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NCU04652 | AP-3 complex subunit delta; Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane. (1060 aa) | ||||
NCU11187 | Signal sequence receptor alpha subunit. (659 aa) | ||||
NCU11209 | Vacuolar protein sorting-associated protein 28; Component of the ESCRT-I complex (endosomal sorting complex required for transport I), a regulator of vesicular trafficking process. (237 aa) | ||||
ti | Oligosaccharyl transferase STT3 subunit. (749 aa) | ||||
NCU11248 | Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the en [...] (283 aa) | ||||
NCU11258 | LYR family protein; Belongs to the complex I LYR family. (99 aa) | ||||
NCU10457 | Uncharacterized protein. (355 aa) | ||||
NCU10762 | UDP-N-acetyl-glucosamine-1-P transferase Alg7. (470 aa) | ||||
NCU11109 | ORM1. (180 aa) | ||||
NCU10618 | AP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (155 aa) | ||||
NCU11313 | Microsomal signal peptidase Spc12. (103 aa) | ||||
tca-12 | Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial; Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (648 aa) | ||||
NCU10430 | SNF7 family protein. (215 aa) | ||||
NCU11370 | 6-phosphogluconate dehydrogenase 2. (306 aa) | ||||
NCU11402 | DUF786 family protein. (130 aa) | ||||
NCU01539 | Vacuolar morphogenesis protein AvaB. (1138 aa) | ||||
NCU03740 | RING-type domain-containing protein. (941 aa) | ||||
NCU01024 | MICOS complex subunit MIC12; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. (313 aa) | ||||
gnb-1 | Guanine nucleotide-binding protein beta subunit. (358 aa) | ||||
NCU08438 | CFEM domain-containing protein. (93 aa) | ||||
NCU03898 | ESCRT-II complex component. (225 aa) | ||||
Nuo19.3 | NADH-ubiquinone oxidoreductase 19.3 kDa subunit, mitochondrial; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (226 aa) | ||||
vma-8 | V-type proton ATPase subunit D; Subunit of the peripheral V1 complex of vacuolar ATPase. V- ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system; Belongs to the V-ATPase D subunit family. (264 aa) | ||||
cox-3 | Cytochrome c oxidase subunit 3; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and t [...] (269 aa) | ||||
oli | ATP synthase subunit 9, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the centr [...] (147 aa) | ||||
cox-1 | Cytochrome c oxidase subunit 1; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and t [...] (557 aa) | ||||
ndh-5 | NADH-ubiquinone oxidoreductase chain 5; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (715 aa) | ||||
cox-4 | Cytochrome c oxidase subunit 4, mitochondrial; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane [...] (186 aa) | ||||
cya-4 | Cytochrome c oxidase subunit 5, mitochondrial; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane [...] (171 aa) | ||||
fes-1 | Cytochrome b-c1 complex subunit Rieske, mitochondrial; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical g [...] (231 aa) | ||||
cyt-1 | Cytochrome c1, heme protein, mitochondrial; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient ove [...] (332 aa) | ||||
Por | Mitochondrial outer membrane protein porin; Forms a channel through the cell membrane that allows diffusion of small hydrophilic molecules. The channel adopts an open conformation at low or zero membrane potential and a closed conformation at potentials above 30-40 mV. The open state has a weak anion selectivity whereas the closed state is cation-selective. (283 aa) | ||||
ndh-1 | NADH-ubiquinone oxidoreductase chain 1; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (371 aa) | ||||
vtr-7 | Small COPII coat GTPase sar1; Small GTPase component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules. Vtr-7/sar1 controls the coat assembly in a stepwise manner. Activated sar1-GTP binds to membranes first and recruits the sec23/24 complex. These sec23/24-sar1 prebudding intermediates are then collected by the sec13/31 complex as subunits polymerize to form coated [...] (189 aa) | ||||
vma-1 | V-type proton ATPase catalytic subunit A; Catalytic subunit of the peripheral V1 complex of vacuolar ATPase. V-ATPase vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (607 aa) | ||||
vma-2 | V-type proton ATPase subunit B; Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells; Belongs to the ATPase alpha/beta chains family. (513 aa) | ||||
Nuo20.8 | NADH-ubiquinone oxidoreductase 20.8 kDa subunit; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (183 aa) | ||||
nuo-49 | NADH-ubiquinone oxidoreductase 49 kDa subunit, mitochondrial; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (478 aa) | ||||
atp-2 | ATP synthase subunit beta, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the c [...] (519 aa) | ||||
nuo-31 | NADH-ubiquinone oxidoreductase 30.4 kDa subunit, mitochondrial; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (283 aa) | ||||
tom40 | Mitochondrial import receptor subunit tom40; Channel-forming protein essential for import of protein precursors into mitochondria; Belongs to the Tom40 family. (349 aa) | ||||
nuo-51 | NADH-ubiquinone oxidoreductase 51 kDa subunit, mitochondrial; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (493 aa) | ||||
nuo-32 | NADH-ubiquinone oxidoreductase 29.9 kDa subunit, mitochondrial; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (273 aa) | ||||
Nuo21.3b | NADH-ubiquinone oxidoreductase 21.3 kDa subunit; Transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (200 aa) | ||||
nuo-21 | NADH-ubiquinone oxidoreductase 21 kDa subunit, mitochondrial; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (218 aa) | ||||
vma-3 | V-type proton ATPase 16 kDa proteolipid subunit; Proton-conducting pore forming subunit of the membrane integral V0 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (161 aa) | ||||
tom20 | Mitochondrial import receptor subunit tom20; Central component of the receptor complex responsible for the recognition and translocation of cytosolically synthesized mitochondrial preproteins. Together with tom22 functions as the transit peptide receptor at the surface of the mitochondrion outer membrane and facilitates the movement of preproteins into the translocation pore. (181 aa) | ||||
atp-1 | ATP synthase subunit alpha, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the [...] (551 aa) | ||||
atp-6 | ATP synthase subunit a; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subuni [...] (261 aa) | ||||
nuo-24 | NADH-ubiquinone oxidoreductase 24 kDa subunit, mitochondrial; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (263 aa) | ||||
nuo14.8 | NADH-ubiquinone oxidoreductase 14.8 kDa subunit; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed to be not involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. The precise function of this subunit is unknown but believed to be important. (124 aa) | ||||
qcr8 | Cytochrome b-c1 complex subunit 8; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inn [...] (107 aa) | ||||
vma-6 | V-type proton ATPase subunit d; Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. The active enzyme consists of a catalytic V1 domain attached to an integral membrane V0 proton pore complex. This subunit is a non-integral membrane component of the membrane pore domain and is required for proper assembly of the V0 sector. Might be involved in the regulated assembly of V1 subunits onto the membrane sector or alternatively may prevent the passage of protons through V0 pores (By similarity); Belongs to the V-ATPase V0D/AC39 subunit family. (364 aa) | ||||
des | ATP synthase subunit delta, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP turnover in the catalytic domain of F(1) is coupled via a rotary mechanism of the c [...] (165 aa) | ||||
tim17 | Mitochondrial import inner membrane translocase subunit tim17; Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane. (155 aa) | ||||
vma-10 | V-type proton ATPase subunit G; Catalytic subunit of the peripheral V1 complex of vacuolar ATPase (V-ATPase). V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (115 aa) | ||||
vma-4 | V-type proton ATPase subunit E; Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (230 aa) | ||||
vph-1 | V-type proton ATPase subunit a; Subunit of the integral membrane V0 complex of vacuolar ATPase essential for assembly and catalytic activity. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells (By similarity). (856 aa) | ||||
cox-6 | Cytochrome c oxidase subunit 6, mitochondrial; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane [...] (148 aa) | ||||
nuo20.9 | NADH-ubiquinone oxidoreductase 20.9 kDa subunit; Transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (189 aa) | ||||
nuo-12.3 | NADH-ubiquinone oxidoreductase 12 kDa subunit, mitochondrial; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity). (104 aa) | ||||
gna-2 | Guanine nucleotide-binding protein alpha-2 subunit; Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems; Belongs to the G-alpha family. G(q) subfamily. (355 aa) | ||||
gna-1 | Guanine nucleotide-binding protein alpha-1 subunit; Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems; Belongs to the G-alpha family. G(q) subfamily. (353 aa) | ||||
tom22 | Mitochondrial import receptor subunit tom22; Central component of the receptor complex responsible for the recognition and translocation of cytosolically synthesized mitochondrial preproteins. Together with tom20 functions as the transit peptide receptor at the surface of the mitochondrion outer membrane and facilitates the movement of preproteins into the translocation pore. Docks tom20 and tom70 for interaction with the general TOM40 import pore (GIP) complex. May regulate the TOM machinery organization, stability and channel gating (By similarity); Belongs to the Tom22 family. (154 aa) | ||||
nuo-10.5 | NADH-ubiquinone oxidoreductase 10.5 kDa subunit; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (94 aa) | ||||
atp-8 | ATP synthase protein 8; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subuni [...] (54 aa) | ||||
atp-9 | ATP synthase subunit 9, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the centr [...] (74 aa) | ||||
nuo21.3c | NADH-ubiquinone oxidoreductase 23 kDa subunit, mitochondrial; Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. May donate electrons to ubiquinone. (219 aa) | ||||
NCU03497 | Plasma membrane iron permease. (422 aa) | ||||
NCU03459 | UBA domain-containing protein Ucp14. (275 aa) | ||||
NCU03558 | Uncharacterized protein. (78 aa) | ||||
NCU01575 | SNARE complex subunit. (292 aa) | ||||
NCU01655 | DUF2012 domain-containing protein. (273 aa) | ||||
iap-1 | Intermembrane space AAA protease IAP-1. (843 aa) | ||||
NCU03344 | Uncharacterized protein. (337 aa) | ||||
cox-15 | Cytochrome c oxidase subunit 8, mitochondrial; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane [...] (82 aa) | ||||
NCU01814 | Uncharacterized protein. (299 aa) | ||||
NCU01791 | SNF7 family protein. (235 aa) | ||||
NCU03440 | AP-2 complex subunit alpha; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (988 aa) | ||||
NCU01783 | Phosphatidylinositol N-acetylglucosaminyltransferase. (263 aa) | ||||
NCU01741 | SNARE complex subunit. (181 aa) | ||||
NCU01739 | Uncharacterized protein. (206 aa) | ||||
acw-5 | Anchored cell wall protein 5. (190 aa) | ||||
NCU09216 | Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit OST2; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the [...] (205 aa) | ||||
NCU04651 | Tetratricopeptide repeat domain-containing protein. (310 aa) | ||||
NCU04633 | RING finger protein. (829 aa) | ||||
pre-2 | Pheromone receptor. (566 aa) | ||||
NCU04165 | Low-temperature viability protein ltv1. (417 aa) | ||||
NCU09673 | AP-2 complex subunit mu-1; Belongs to the adaptor complexes medium subunit family. (437 aa) | ||||
NCU08939 | Mannan polymerase II complex ANP1 subunit. (404 aa) | ||||
NCU06713 | Vacuolar protein sorting protein 55. (128 aa) | ||||
NCU06708 | Protein transporter sec22; Belongs to the synaptobrevin family. (217 aa) | ||||
NCU04188 | UPF0220 domain-containing protein. (173 aa) | ||||
syn-2 | Syntaxin 2. (335 aa) | ||||
NCU04121 | AP-1 complex subunit gamma. (842 aa) | ||||
NCU04119 | SNARE complex subunit; Belongs to the syntaxin family. (362 aa) | ||||
NCU04115 | Clathrin light chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin light chain family. (244 aa) | ||||
NCU03623 | Ubiquitin-conjugating enzyme E; Belongs to the ubiquitin-conjugating enzyme family. (166 aa) | ||||
NCU03605 | Amidohydrolase. (453 aa) | ||||
NCU01002 | Coatomer subunit epsilon; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. The coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. Belongs to the COPE family. (296 aa) | ||||
NCU06856 | Ubiquitin fusion degradation protein. (382 aa) | ||||
cox-13 | Cytochrome c oxidase subunit 12, mitochondrial; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane [...] (84 aa) | ||||
NCU06777 | Syntaxin; Belongs to the syntaxin family. (275 aa) | ||||
tim44 | Mitochondrial import inner membrane translocase subunit TIM44; Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner; Belongs to the Tim44 family. (526 aa) | ||||
cob | Cytochrome b; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that driv [...] (385 aa) | ||||
NCU16010 | Probable intron-encoded endonuclease 3; Mitochondrial DNA endonuclease involved in intron homing. In the C-terminal section; belongs to the LAGLIDADG endonuclease family. (533 aa) | ||||
NCU16011 | Probable intron-encoded endonuclease 4; Mitochondrial DNA endonuclease involved in intron homing. In the C-terminal section; belongs to the LAGLIDADG endonuclease family. (545 aa) | ||||
map-1 | Matrix AAA protease MAP-1. (928 aa) | ||||
NCU09688 | AP-1 complex subunit mu; Belongs to the adaptor complexes medium subunit family. (448 aa) | ||||
NCU01822 | Vacuolar protein sorting-associated protein 29; Belongs to the VPS29 family. (239 aa) | ||||
NCU05069 | FAD dependent oxidoreductase. (551 aa) | ||||
gng-1 | Guanine nucleotide-binding protein subunit gamma; Belongs to the G protein gamma family. (93 aa) | ||||
NCU00493 | Coatomer subunit delta; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (512 aa) | ||||
nuo18.4 | NADH:ubiquinone oxidoreductase 18.4kD subunit. (165 aa) | ||||
NCU04346 | Uncharacterized protein. (618 aa) | ||||
NCU04345 | Adaptin ear-binding coat-associated protein 2. (274 aa) | ||||
tim14 | Mitochondrial import inner membrane translocase subunit tim14; Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. In the complex, it is required to stimulate activity of mtHSP70 (hsp70-5) (By similarity); Belongs to the TIM14 family. (105 aa) | ||||
NCU00184 | Uncharacterized protein. (384 aa) | ||||
NCU05060 | CFEM domain-containing protein. (468 aa) | ||||
NCU03995 | Oligosaccharyl transferase subunit. (330 aa) | ||||
NCU00169 | Translocation complex component. (700 aa) | ||||
NCU00435 | SNF7 family protein. (227 aa) | ||||
NCU00447 | Serine palmitoyltransferase 2. (663 aa) | ||||
sec11 | Signal peptidase complex catalytic subunit sec11; Catalytic component of the signal peptidase complex (SPC), which catalyzes the cleavage of N-terminal signal sequences of proteins targeted to the endoplasmic reticulum. Signal peptide cleavage occurs during the translocation (cotranslationally or post-translationally) through the translocon pore into the endoplasmic reticulum (By similarity). (172 aa) | ||||
mic10 | MICOS complex subunit mic10; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. (93 aa) | ||||
NCU00126 | Erf4 domain-containing protein. (257 aa) | ||||
NCU04404 | Coatomer subunit beta; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (957 aa) | ||||
gem-1 | Mitochondrial Rho GTPase 1; Mitochondrial GTPase involved in mitochondrial trafficking. Probably involved in control of anterograde transport of mitochondria and their subcellular distribution. (629 aa) | ||||
nup-20 | Protein transport protein sec13; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules. It also functions as a component of the nuclear pore complex (NPC). NPC components, collectively referred to as nucleoporins (NUPs), can play the role of both NPC structural components and of docking or interaction partners for transiently associated nuclear transport facto [...] (304 aa) | ||||
NCU03998 | Adaptor protein complex 3 Mu3A; Belongs to the adaptor complexes medium subunit family. (568 aa) | ||||
mdm34 | Mitochondrial distribution and morphology protein 34; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum (ER) and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis, and function in nonvesicular lipid trafficking between the ER and mitochondria. Mdm34 is required for the interaction of the ER-resident membrane protein mmm-1 and the outer mitochondrial membrane-resident beta-barrel protein mdm10. (615 aa) | ||||
cpr-8 | Calpain-like protease palB/cpr-8; Required for the proteolytic cleavage of the transcription factor pacc-1 in response to alkaline ambient pH. (932 aa) | ||||
NCU00290 | ABC transporter. (659 aa) | ||||
NCU00242 | V-SNARE. (562 aa) | ||||
NCU10066 | Coatomer subunit alpha; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. (1223 aa) | ||||
do | 1,3-beta-glucan synthase component GLS1. (1955 aa) | ||||
NCU06870 | Serine palmitoyl CoA transferase subunit LcbA. (521 aa) | ||||
NCU07513 | Uncharacterized protein. (1325 aa) | ||||
NCU07363 | Uncharacterized protein. (349 aa) | ||||
NCU06868 | Sec23/Sec24 family protein. (1052 aa) | ||||
nuo20.1 | NADH:ubiquinone oxidoreductase 20.1kD subunit. (177 aa) | ||||
NCU09459 | Uncharacterized protein. (647 aa) | ||||
gpig-1 | Glycosylphosphatidylinositol anchor N-acetylglucosamine transferase. (534 aa) | ||||
nuo14 | NADH:ubiquinone oxidoreductase 14kD subunit. (121 aa) | ||||
tca-11 | Succinate dehydrogenase cytochrome b560 subunit. (180 aa) | ||||
NCU07746 | F-box domain-containing protein. (216 aa) | ||||
NCU07745 | Uncharacterized protein. (893 aa) | ||||
NCU09055 | CFEM domain-containing protein. (89 aa) | ||||
NCU05959 | Vesicle transport V-SNARE protein VTI1. (228 aa) | ||||
vma-5 | V-type proton ATPase subunit C; Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit C is necessary for the assembly of the catalytic sector of the enzyme and is likely to have a specific function in its catalytic activity. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (391 aa) | ||||
NCU09143 | Uncharacterized protein. (99 aa) | ||||
NCU09121 | Vacuolar sorting protein; Belongs to the STXBP/unc-18/SEC1 family. (666 aa) | ||||
NCU09119 | ATP synthase subunit gamma. (299 aa) | ||||
NCU09721 | AP complex subunit beta; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (749 aa) | ||||
NCU09713 | Uncharacterized protein. (281 aa) | ||||
nuo10.6 | NADH:ubiquinone oxidoreductase 10.6kD subunit. (93 aa) | ||||
NCU09210 | Dyp-type peroxidase. (513 aa) | ||||
NCU08217 | SRP receptor beta subunit. (440 aa) | ||||
NCU04943 | Protein transport protein BOS1; SNARE required for protein transport between the ER and the Golgi complex. (264 aa) | ||||
NCU05902 | Vacuolar assembly protein. (1359 aa) | ||||
NCU05899 | Flotillin domain-containing protein; Belongs to the band 7/mec-2 family. Flotillin subfamily. (525 aa) | ||||
stk-14 | Serine/threonine kinase IREI. (1208 aa) | ||||
NCU06033 | GPI transamidase component PIG-S. (568 aa) | ||||
NCU08166 | MCU domain-containing protein. (493 aa) | ||||
sec24 | Protein transport protein sec24; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules (By similarity). (950 aa) | ||||
NCU02368 | Rhomboid protein 2. (617 aa) | ||||
NCU02293 | Uncharacterized protein. (117 aa) | ||||
NCU05817 | Uncharacterized protein. (311 aa) | ||||
tkl-1 | Serine/threonine protein kinase. (514 aa) | ||||
NCU07061 | Uncharacterized protein. (177 aa) | ||||
gpit-1 | GPI transamidase component GPI16. (632 aa) | ||||
nuo9.8 | NADH:ubiquinone oxidoreductase 9.8 kDa subunit. (86 aa) | ||||
un-4 | Mitochondrial import inner membrane translocase subunit tim16; Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. In the complex, it is required to regulate activity of mtHSP70 (hsp70-5) via its interaction with tim14/pam18. May act by positioning tim14/pam18 in juxtaposition to mtHSP70 at the translocon to maximize ATPase stimulation (By similarity); Belongs to the TIM16/PAM16 family. (141 aa) | ||||
NCU05582 | Ubiquitin fusion degradation protein. (784 aa) | ||||
NCU06677 | Signal peptidase subunit 3. (227 aa) | ||||
NCU01199 | SNARE domain-containing protein. (259 aa) | ||||
NCU08689 | Polyphosphoinositide phosphatase Fig4. (1190 aa) | ||||
NCU05160 | ATP-dependent Zn protease. (486 aa) | ||||
NCU05232 | AP complex subunit beta; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (748 aa) | ||||
NCU05231 | ER membrane protein complex subunit 4; Belongs to the EMC4 family. (190 aa) | ||||
NCU05228 | Rad60-SLD_2 domain-containing protein. (264 aa) | ||||
NCU05220 | ATP synthase subunit F. (101 aa) | ||||
NCU06588 | Uncharacterized protein. (181 aa) | ||||
NCU08811 | Arf GTPase-activating protein. (496 aa) | ||||
tim21 | Mitochondrial import inner membrane translocase subunit tim21; Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane. Required to keep the TOM and the TIM23 complexes in close contact. At some point, it is released from the TOM23 complex to allow protein translocation into the mitochondrial matrix (By similarity). (251 aa) | ||||
NCU07962 | CFEM domain-containing protein. (234 aa) | ||||
NCU07260 | Uncharacterized protein. (851 aa) | ||||
NCU07259 | GPI-anchor transamidase; Mediates GPI anchoring in the endoplasmic reticulum, by replacing a protein's C-terminal GPI attachment signal peptide with a pre-assembled GPI. During this transamidation reaction, the GPI transamidase forms a carbonyl intermediate with the substrate protein. Belongs to the peptidase C13 family. (401 aa) | ||||
NCU07020 | Vacuolar protein sorting-associated protein vps17. (662 aa) | ||||
NCU06569 | AP-3 adaptor complex subunit beta. (805 aa) | ||||
NCU06560 | HTH APSES-type domain-containing protein. (484 aa) | ||||
vma-9 | Vacuolar ATPase subunit E. (75 aa) | ||||
stk-45 | Phosphoinositide 3-kinase regulatory subunit 4. (1563 aa) | ||||
NCU06595 | Vacuolar protein sorting protein. (637 aa) | ||||
NCU07939 | Syntaxin. (360 aa) | ||||
NCU07319 | Coatomer subunit beta; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (858 aa) | ||||
NCU06331 | Uncharacterized protein. (448 aa) | ||||
NCU06284 | Vacuolar protein sorting-associated protein 35; Plays a role in vesicular protein sorting. (881 aa) | ||||
NCU08024 | Mannan polymerase II complex ANP1 subunit. (481 aa) | ||||
aps-2 | AP-2 complex subunit sigma; Component of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration (By similarity). (143 aa) | ||||
NCU06268 | Probable vacuolar protein sorting-associated protein 16 homolog; Essential for vacuolar protein sorting. Required for vacuole biogenesis, stability and to maintain vacuole morphology. (865 aa) | ||||
mdm10 | Mitochondrial distribution and morphology protein 10; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis and may function in phospholipid exchange. mdm10 is involved in the late assembly steps of the general translocase of the mitochondrial outer membrane (TOM complex). Functions in the tom40-specific route of the assembly of outer membrane beta-barrel proteins, including the association of tom40 with the recepto [...] (480 aa) | ||||
NCU06183 | Vacuolar protein sorting protein DigA. (973 aa) | ||||
NCU08538 | HNHc domain-containing protein. (407 aa) | ||||
nor-1 | NADPH oxidase regulator NoxR. (517 aa) | ||||
NCU07843 | Vacuolar-sorting protein SNF8; Component of the endosomal sorting complex required for transport II (ESCRT-II), which is required for multivesicular body (MVB) formation and sorting of endosomal cargo proteins into MVBs. Belongs to the SNF8 family. (267 aa) | ||||
NCU09461 | AP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (194 aa) | ||||
NCU05422 | E3 ubiquitin-protein ligase PEP5. (1016 aa) | ||||
smco-1 | Calcium channel subunit Cch1. (2218 aa) | ||||
NCU09386 | Uncharacterized protein. (145 aa) | ||||
NCU09332 | Mannosyltransferase PMTI. (774 aa) | ||||
NCU08382 | Peroxisomal half ABC transporter. (865 aa) | ||||
NCU02635 | Mannan polymerase complexes MNN9 subunit. (373 aa) | ||||
NCU00527 | Mitochondrial genome maintenance protein Mgr2. (115 aa) | ||||
NCU01928 | UBX domain-containing protein. (514 aa) | ||||
NCU00753 | Uncharacterized protein. (444 aa) | ||||
NCU02137 | Phosphatidylinositol:UDP-GlcNAc transferase PIG-C. (701 aa) | ||||
atp-3 | ATP synthase subunit 4, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the cent [...] (241 aa) | ||||
pam17 | Presequence translocated-associated motor subunit pam17, mitochondrial; Component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. (267 aa) | ||||
NCU00725 | Epsin-3. (521 aa) | ||||
vma-16 | Vacuolar ATPase proteolipid subunit; Belongs to the V-ATPase proteolipid subunit family. (200 aa) | ||||
NCU02147 | Ankyrin repeat and zinc finger domain-containing protein 1. (649 aa) | ||||
NCU02083 | 1-phosphatidylinositol-3-phosphate 5-kinase. (2558 aa) | ||||
mdm12 | Mitochondrial distribution and morphology protein 12; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum (ER) and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis, and function in nonvesicular lipid trafficking between the ER and mitochondria. Mdm12 is required for the interaction of the ER-resident membrane protein MMM1 and the outer mitochondrial membrane-resident beta-barrel protein mdm10. The mdm12-mmm-1 subcomplex functions in the major beta-barrel assembly pa [...] (675 aa) | ||||
NCU02064 | MICOS complex subunit; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. (280 aa) | ||||
NCU09243 | Uncharacterized protein. (388 aa) | ||||
NCU00566 | Synaptobrevin. (116 aa) | ||||
gpit-2 | Glycosylphosphatidylinositol transamidase 2. (427 aa) | ||||
tob37 | Topogenesis of outer membrane beta barrel protein 37. (442 aa) | ||||
mic60 | MICOS complex subunit mic60; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. Plays a role in keeping cristae membranes connected to the inner boundary membrane. Also promotes protein import via the mitochondrial intermembrane space assembly (MIA) pathway (By similarity). (672 aa) | ||||
NCU01992 | Coatomer subunit gamma; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (916 aa) | ||||
vma-13 | V-type proton ATPase subunit H; Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit H activates ATPase activity of the enzyme and couples ATPase activity to proton flow. Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system. (481 aa) | ||||
NCU02743 | Vacuolar protein sorting protein 26. (327 aa) | ||||
NCU00966 | ER membrane protein complex subunit 3; The EMC seems to be required for efficient folding of proteins in the endoplasmic reticulum (ER). Belongs to the EMC3 family. (259 aa) | ||||
NCU00965 | Uncharacterized protein. (245 aa) | ||||
NCU08093 | Uncharacterized protein. (63 aa) | ||||
NCU08379 | Protein transport protein Sec61 subunit beta; Necessary for protein translocation in the endoplasmic reticulum. (114 aa) | ||||
qcr9 | Cytochrome b-c1 complex subunit 9, mitochondrial; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradie [...] (59 aa) | ||||
NCU03199 | ATP synthase subunit H. (124 aa) | ||||
NCU03198 | DOMON domain-containing protein. (428 aa) | ||||
Tca-13 | Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial; Membrane-anchoring subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q); Belongs to the CybS family. (166 aa) | ||||
NCU02706 | Golgi SNAP receptor complex member 1; Involved in transport from the ER to the Golgi apparatus as well as in intra-Golgi transport. It belongs to a super-family of proteins called t-SNAREs or soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein receptor. (227 aa) | ||||
NCU02681 | Translocation protein. (221 aa) | ||||
npl4 | Nuclear protein localization protein 4; Involved in the import of nuclear-targeted proteins into the nucleus and the export of poly(A) RNA out of the nucleus. Has a role in the endoplasmic reticulum-associated degradation (ERAD) pathway (By similarity); Belongs to the NPL4 family. (660 aa) | ||||
NCU02676 | DUF1746 domain-containing protein. (373 aa) | ||||
snx-3 | Sorting nexin-3; Required for retention of late Golgi membrane proteins. Component of the retrieval machinery that functions by direct interaction with the cytosolic tails of certain TGN membrane proteins during the sorting/budding process at the prevacuolar compartment. Binds phosphatidylinositol 3-phosphate (PtdIns(P3)) (By similarity). (142 aa) | ||||
NCU01907 | Syntaxin 5. (317 aa) | ||||
NCU02541 | Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the en [...] (501 aa) | ||||
NCU02538 | Coatomer subunit zeta; The zeta subunit may be involved in regulating the coat assembly and, hence, the rate of biosynthetic protein transport due to its association-dissociation properties with the coatomer complex. (208 aa) | ||||
NCU02510 | Clathrin heavy chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin heavy chain family. (1678 aa) | ||||
NCU00669 | Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit WBP1; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the [...] (466 aa) | ||||
NCU00656 | Phosphatidylinositol 3-kinase VPS34. (914 aa) | ||||
NCU00644 | ATP synthase subunit G. (187 aa) | ||||
atp7 | ATP synthase subunit d, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the cent [...] (173 aa) | ||||
NCU00614 | DUF1620 domain-containing protein. (972 aa) | ||||
och-1 | Initiation-specific alpha-1,6-mannosyltransferase. (372 aa) | ||||
sec-61 | Protein transport protein SEC61 subunit alpha; Appears to play a crucial role in the insertion of secretory and membrane polypeptides into the ER. It is required for assembly of membrane and secretory proteins and is essential for cell growth. It interacts with other membrane proteins required for protein translocation. Upon binding to SEC62/63 complex, secretory precursor polypeptides may engage SEC61 to begin membrane penetration event. A cycle of assembly and disassembly of SEC62/63 from SEC61 may govern the activity of the translocase (By similarity). (476 aa) | ||||
qcr7 | Cytochrome b-c1 complex subunit 7; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inn [...] (123 aa) | ||||
vsp-3 | Vacuolar-sorting protein snf7; Required for the sorting and concentration of proteins resulting in the entry of these proteins into the invaginating vesicles of the multivesicular body (MVB). Also required for the proteolytic cleavage of the transcription factor pacc-1 in response to alkaline ambient pH (By similarity). (228 aa) | ||||
cyn1 | Cyanate hydratase; Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide; Belongs to the cyanase family. (164 aa) | ||||
sec31 | Protein transport protein sec31; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules (By similarity). (1256 aa) | ||||
tim50 | Mitochondrial import inner membrane translocase subunit tim50; Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane. Required to direct preproteins in transit and direct them to the channel protein tim23, and possibly facilitates transfer of the translocating proteins from the TOM complex to the TIM23 complex. (540 aa) | ||||
tim10 | Mitochondrial import inner membrane translocase subunit tim10; Mitochondrial intermembrane chaperone that participates in the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. Also required for the transfer of beta- barrel precursors from the TOM complex to the sorting and assembly machinery (SAM complex) of the outer membrane. Acts as a chaperone-like protein that protects the hydrophobic precursors from aggregation and guide them through the mitochondrial intermembrane space. Belongs to the small Tim family. (90 aa) | ||||
tim54 | Mitochondrial import inner membrane translocase subunit tim54; Essential component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. The TIM22 complex forms a twin- pore translocase that uses the membrane potential as external driving force (By similarity). (468 aa) | ||||
tim22 | Mitochondrial import inner membrane translocase subunit tim22; Essential core component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. In the TIM22 complex, it constitutes the voltage-activated and signal-gated channel. Forms a twin-pore translocase that uses the membrane potential as external driving force in 2 voltage-dependent steps (By similarity). (194 aa) | ||||
sec23-1 | Protein transport protein sec23; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules (By similarity). (775 aa) | ||||
9G6.310 | Probable protein transport protein Sec61 subunit gamma; Necessary for protein translocation in the endoplasmic reticulum. (70 aa) | ||||
gna-3 | Guanine nucleotide-binding protein alpha-3 subunit; Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. Involved in conidiation; Belongs to the G-alpha family. G(q) subfamily. (356 aa) | ||||
mmm-1 | Maintenance of mitochondrial morphology protein 1; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum (ER) and mitochondria (By similarity). Components of this complex are involved in the control of mitochondrial shape and protein biogenesis, and function in nonvesicular lipid trafficking between the ER and mitochondria. The mdm12-mmm-1 subcomplex functions in the major beta-barrel assembly pathway that is responsible for biogenesis of all outer membrane beta-barrel proteins, and acts in a late step after the SAM complex. The mdm [...] (415 aa) | ||||
grpe | GrpE protein homolog, mitochondrial; Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. Seems to control the nucleotide-dependent binding of mtHSP70 (hsp70-5) to substrate proteins (By similarity). (238 aa) | ||||
atp-5 | ATP synthase subunit 5, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the centr [...] (220 aa) | ||||
B1D1.150 | Probable vesicular-fusion protein sec17 homolog; Required for vesicular transport between the endoplasmic reticulum and the Golgi apparatus; Belongs to the SNAP family. (292 aa) | ||||
vma-7 | V-type proton ATPase subunit F; Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells (By similarity). (124 aa) | ||||
vma-11 | V-type proton ATPase 16 kDa proteolipid subunit 2; Proton-conducting pore forming subunit of the membrane integral V0 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells (By similarity). (167 aa) | ||||
tim23 | Mitochondrial import inner membrane translocase subunit tim23. (238 aa) | ||||
NCU00018 | Cell division control protein Cdc48, variant; Belongs to the AAA ATPase family. (824 aa) | ||||
syn-1 | Syntaxin family protein. (473 aa) | ||||
NCU02409 | Uncharacterized protein. (892 aa) | ||||
tob55 | Mitochondrial outer membrane beta-barrel protein Tob55. (521 aa) | ||||
NCU02255 | N-acetylglucosaminyl transferase component Gpi1. (717 aa) | ||||
nuo13.4 | NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (216 aa) | ||||
tom7 | TOM7, variant 1. (53 aa) | ||||
qcr6 | Cytochrome b-c1 complex subunit 6, mitochondrial; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradie [...] (141 aa) | ||||
NCU01283 | Uncharacterized protein. (1354 aa) | ||||
NCU02351 | Chitin synthase regulator 3, variant 1. (935 aa) | ||||
NCU08948 | NIF domain-containing protein, variant. (531 aa) | ||||
NCU08961 | Uncharacterized protein. (1047 aa) | ||||
NCU05195 | Uncharacterized protein. (484 aa) | ||||
NCU17017 | Mitochondrial inner membrane protease subunit. (321 aa) | ||||
NCU01854 | Uncharacterized protein. (214 aa) | ||||
NCU16844 | Cytochrome b-c1 complex subunit 10, mitochondrial; Component of the ubiquinol-cytochrome c oxidoreductase, a multisubunit transmembrane complex that is part of the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradi [...] (91 aa) | ||||
NCU02718 | Uncharacterized protein. (692 aa) | ||||
tob38 | Mitochondrial outer membrane protein, variant. (340 aa) | ||||
NCU01436 | Questionable protein, variant. (83 aa) | ||||
NCU04212 | Uncharacterized protein. (511 aa) | ||||
NCU08300 | Uncharacterized protein. (91 aa) | ||||
NCU16791 | Mitochondrial inner membrane protease subunit 2. (184 aa) | ||||
eat-5 | Cytochrome c oxidase subunit 13, mitochondrial; Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol- cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane [...] (136 aa) |