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Q5KPQ9_CRYNJ | AP-1 complex subunit gamma. (854 aa) | ||||
Q5KPR9_CRYNJ | ER membrane protein complex subunit 4; Belongs to the EMC4 family. (197 aa) | ||||
Q5KPS5_CRYNJ | Vacuolar protein sorting-associated protein 29; Belongs to the VPS29 family. (203 aa) | ||||
A0A0S2LHW3 | Uncharacterized protein. (52 aa) | ||||
A0A0S2LI43 | Uncharacterized protein. (326 aa) | ||||
A0A0S2LII0 | Uncharacterized protein. (90 aa) | ||||
A0A0S2LIJ5 | Uncharacterized protein. (226 aa) | ||||
A0A0S2LIL8 | Uncharacterized protein. (143 aa) | ||||
A0A0S2LIR2 | Uncharacterized protein. (336 aa) | ||||
A0A0S2LIT1 | FCP1 homology domain-containing protein. (495 aa) | ||||
A0A0S2LIX3 | Uncharacterized protein. (206 aa) | ||||
A0A0S2LIY7 | V-SNARE coiled-coil homology domain-containing protein. (154 aa) | ||||
A0A0S2M5A9 | G protein gamma domain-containing protein. (87 aa) | ||||
A0A0S2M5L1 | Uncharacterized protein. (220 aa) | ||||
A0A0S2M5R0 | Uncharacterized protein. (208 aa) | ||||
A0A0S2M5Z0 | G protein gamma domain-containing protein. (81 aa) | ||||
A0A0S2M611 | Uncharacterized protein. (293 aa) | ||||
A0A0S2M691 | Ubiquitin-like domain-containing protein. (511 aa) | ||||
ALG14 | UDP-N-acetylglucosamine transferase subunit ALG14; Involved in protein N-glycosylation. Essential for the second step of the dolichol-linked oligosaccharide pathway. Anchors the catalytic subunit ALG13 to the ER (By similarity). (229 aa) | ||||
CYN1 | Cyanate hydratase; Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide; Belongs to the cyanase family. (183 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 (By similarity). (516 aa) | ||||
GPA1 | Guanine nucleotide-binding protein subunit alpha; Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. Involved in the mating pathway; Belongs to the G-alpha family. (432 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 [...] (508 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-MMM1 subcomplex functions in the major beta-barrel assembly pat [...] (388 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 MMM1 and the outer mitochondrial membrane-resident beta-barrel protein MDM10. (343 aa) | ||||
MMM1 | 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. 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-MMM1 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 MDM10-MDM12-MMM1 su [...] (475 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. (693 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. (217 aa) | ||||
SAR1 | 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. 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 trans [...] (189 aa) | ||||
SEC23 | 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). (763 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); Belongs to the SEC23/SEC24 family. SEC24 subfamily. (920 aa) | ||||
SNF7 | 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 RIM101 in response to alkaline ambient pH (By similarity). (220 aa) | ||||
SNX3 | 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). (144 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). (187 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). (458 aa) | ||||
TIM9 | Mitochondrial import inner membrane translocase subunit TIM9; 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 (By similarity); Belongs to the small Tim family. (89 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 (By similarity); Belongs to the small Tim family. (102 aa) | ||||
SEC13 | 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 [...] (339 aa) | ||||
Q5K6T7_CRYNJ | 1,3-beta-glucan synthase, putative. (1801 aa) | ||||
Q5K6T9_CRYNJ | Expressed protein. (475 aa) | ||||
Q5K6Y2_CRYNJ | Response to unfolded-protein, putative. (277 aa) | ||||
Q5K6Z4_CRYNJ | Signal peptidase subunit 3. (199 aa) | ||||
Q5K701_CRYNJ | 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. (99 aa) | ||||
Q5K720_CRYNJ | AP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (143 aa) | ||||
Q5K728_CRYNJ | Expressed protein. (71 aa) | ||||
Q5K757_CRYNJ | E3 ubiquitin-protein ligase PEP5. (1071 aa) | ||||
Q5K779_CRYNJ | Protein transport protein Sec61 subunit beta; Necessary for protein translocation in the endoplasmic reticulum. (100 aa) | ||||
Q5K7H4_CRYNJ | Uncharacterized protein. (441 aa) | ||||
Q5K7H5_CRYNJ | Acidic laccase, putative; Belongs to the multicopper oxidase family. (640 aa) | ||||
Q5K7J0_CRYNJ | Uncharacterized protein. (131 aa) | ||||
Q5K7M2_CRYNJ | t-SNARE coiled-coil homology domain-containing protein. (356 aa) | ||||
Q5K7N6_CRYNJ | Uncharacterized protein. (179 aa) | ||||
Q5K7Q5_CRYNJ | PIPK domain-containing protein. (1821 aa) | ||||
Q5K7S8_CRYNJ | zf-CHCC domain-containing protein. (144 aa) | ||||
Q5K7X0_CRYNJ | ER to Golgi transport-related protein, putative. (1003 aa) | ||||
Q5K7Z1_CRYNJ | Expressed protein. (682 aa) | ||||
Q5K822_CRYNJ | Expressed protein. (531 aa) | ||||
Q5K888_CRYNJ | Ubiquitin fusion-degradation 1-like protein, putative. (481 aa) | ||||
Q5K889_CRYNJ | t-SNARE, putative; Belongs to the syntaxin family. (409 aa) | ||||
Q5K8G6_CRYNJ | Uncharacterized protein. (235 aa) | ||||
Q5K8H0_CRYNJ | Uncharacterized protein. (114 aa) | ||||
Q5K8J0_CRYNJ | Expressed protein. (74 aa) | ||||
Q5K8K8_CRYNJ | 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. (725 aa) | ||||
Q5K8L7_CRYNJ | ENTH domain-containing protein. (494 aa) | ||||
Q5K8Q1_CRYNJ | Cytochrome c oxidase polypeptide iv, mitochondrial, putative. (158 aa) | ||||
VMA9 | V-type proton ATPase subunit e; Subunit of the integral membrane V0 complex of vacuolar ATPase (By similarity). V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (71 aa) | ||||
Q5K8T1_CRYNJ | Expressed protein. (312 aa) | ||||
Q5K8U4_CRYNJ | Ubiquinol-cytochrome C reductase complex core protein 2, putative. (434 aa) | ||||
Q5K8W3_CRYNJ | NADH-ubiquinone oxidoreductase; 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. (155 aa) | ||||
Q5K8Y5_CRYNJ | Uncharacterized protein. (435 aa) | ||||
Q5K906_CRYNJ | 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. (755 aa) | ||||
Q5K938_CRYNJ | V-type proton ATPase 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. (167 aa) | ||||
Q5K946_CRYNJ | Cytochrome c oxidase subunit V, putative. (167 aa) | ||||
Q5K9E5_CRYNJ | Grpe protein, putative; Belongs to the GrpE family. (228 aa) | ||||
Q5K9H6_CRYNJ | Chloride channel protein. (864 aa) | ||||
Q5K9K1_CRYNJ | Uncharacterized protein. (1535 aa) | ||||
Q5K9K5_CRYNJ | Uncharacterized protein. (361 aa) | ||||
Q5K9Y4_CRYNJ | UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase, putative. (502 aa) | ||||
Q5KA21_CRYNJ | Integral membrane protein sed5, putative. (364 aa) | ||||
Q5KA29_CRYNJ | Clathrin heavy chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin heavy chain family. (1684 aa) | ||||
Q5KA71_CRYNJ | MMS2, putative; Belongs to the AAA ATPase family. (810 aa) | ||||
Q5KA77_CRYNJ | Mitochondrial import receptor subunit tom22, putative. (149 aa) | ||||
Q5KAA7_CRYNJ | Hydrogen-transporting ATPase, putative; Belongs to the V-ATPase proteolipid subunit family. (198 aa) | ||||
Q5KAB5_CRYNJ | Structural molecule, putative. (1440 aa) | ||||
Q5KAG9_CRYNJ | 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 [...] (468 aa) | ||||
Q5KAJ6_CRYNJ | 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 [...] (480 aa) | ||||
Q5KAU1_CRYNJ | Uncharacterized protein. (181 aa) | ||||
Q5KAX9_CRYNJ | Ferro-O2-oxidoreductase, putative; Belongs to the multicopper oxidase family. (632 aa) | ||||
Q5KB19_CRYNJ | SNAP receptor, putative. (269 aa) | ||||
Q5KB78_CRYNJ | Voltage-gated potassium channel beta-2 subunit, putative. (355 aa) | ||||
Q5KBA0_CRYNJ | 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). (637 aa) | ||||
Q5KBG5_CRYNJ | Mitochondrial import inner membrane translocase subunit tim17, putative. (161 aa) | ||||
Q5KBG8_CRYNJ | Expressed protein. (72 aa) | ||||
Q5KBH1_CRYNJ | Vacuolar protein sorting-associated protein 41; Required for vacuolar assembly and vacuolar traffic. Belongs to the VPS41 family. (1038 aa) | ||||
Q5KBI9_CRYNJ | Expressed protein. (518 aa) | ||||
Q5KBP6_CRYNJ | LRRNT_2 domain-containing protein. (840 aa) | ||||
Q5KBP7_CRYNJ | Uncharacterized protein. (821 aa) | ||||
Q5KBR2_CRYNJ | Uncharacterized protein. (123 aa) | ||||
Q5KBR3_CRYNJ | Trafficking-related protein, putative. (130 aa) | ||||
Q5KBW0_CRYNJ | Vacuolar proton pump subunit B; Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase; Belongs to the ATPase alpha/beta chains family. (515 aa) | ||||
Q5KC20_CRYNJ | Clathrin light chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin light chain family. (288 aa) | ||||
Q5KC44_CRYNJ | GPI-anchor transamidase, putative. (553 aa) | ||||
Q5KC66_CRYNJ | Expressed protein. (408 aa) | ||||
Q5KC69_CRYNJ | Protein transporter, putative. (478 aa) | ||||
Q5KCD5_CRYNJ | Rab guanyl-nucleotide exchange factor, putative. (570 aa) | ||||
Q5KCF2_CRYNJ | GPI anchor biosynthesis-related protein, putative. (534 aa) | ||||
Q5KCH4_CRYNJ | NADH dehydrogenase 10.5K chain, putative. (100 aa) | ||||
Q5KCK0_CRYNJ | RING-type domain-containing protein. (740 aa) | ||||
Q5KCK9_CRYNJ | Uncharacterized protein. (251 aa) | ||||
Q5KCR0_CRYNJ | Expressed protein. (236 aa) | ||||
Q5KCT8_CRYNJ | Uncharacterized protein. (346 aa) | ||||
Q5KCX6_CRYNJ | Syntaxin, putative. (352 aa) | ||||
Q5KCZ2_CRYNJ | NADH-ubiquinone oxidoreductase, putative; Belongs to the complex I 49 kDa subunit family. (452 aa) | ||||
Q5KCZ3_CRYNJ | Ubiquinol-cytochrome c reductase complex 7.3 kDa protein, putative. (66 aa) | ||||
Q5KD38_CRYNJ | ARF GTPase activator, putative. (479 aa) | ||||
Q5KD54_CRYNJ | Uncharacterized protein. (289 aa) | ||||
Q5KD71_CRYNJ | V-SNARE, putative. (120 aa) | ||||
Q5KDA3_CRYNJ | 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. (755 aa) | ||||
Q5KDB1_CRYNJ | Uncharacterized protein. (167 aa) | ||||
Q5KDM0_CRYNJ | Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial; Iron-sulfur protein (IP) 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). (289 aa) | ||||
Q5KDT1_CRYNJ | 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. (238 aa) | ||||
Q5KDU1_CRYNJ | Expressed protein. (90 aa) | ||||
Q5KDU2_CRYNJ | 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. (952 aa) | ||||
Q5KDU5_CRYNJ | Cytoplasm protein, putative. (604 aa) | ||||
Q5KDU9_CRYNJ | t-SNARE coiled-coil homology domain-containing protein. (229 aa) | ||||
Q5KDW0_CRYNJ | Clathrin assembly protein AP47, putative; Belongs to the adaptor complexes medium subunit family. (435 aa) | ||||
Q5KE76_CRYNJ | Uncharacterized protein. (216 aa) | ||||
Q5KE79_CRYNJ | Uncharacterized protein. (573 aa) | ||||
Q5KEA9_CRYNJ | Uncharacterized protein. (1214 aa) | ||||
Q5KED1_CRYNJ | Osmosensor, putative. (1883 aa) | ||||
Q5KEF7_CRYNJ | 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. (1047 aa) | ||||
Q5KEH2_CRYNJ | Uncharacterized protein. (170 aa) | ||||
Q5KQ38_CRYNJ | Uncharacterized protein. (70 aa) | ||||
Q5KEH7_CRYNJ | 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. (1222 aa) | ||||
Q5KEN2_CRYNJ | Adaptin_N domain-containing protein. (859 aa) | ||||
Q5KEQ0_CRYNJ | Endoplasmic reticulum protein, putative. (1022 aa) | ||||
Q5KEW4_CRYNJ | Mitochondrion protein, putative. (566 aa) | ||||
Q5KEX5_CRYNJ | 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. (454 aa) | ||||
Q5KEZ5_CRYNJ | 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. (415 aa) | ||||
Q5KEZ7_CRYNJ | Uncharacterized protein. (268 aa) | ||||
Q5KF04_CRYNJ | UCR_hinge domain-containing protein. (126 aa) | ||||
Q5KF23_CRYNJ | NADH-ubiquinone oxidoreductase 30.4 kDa subunit, putative; Belongs to the complex I 30 kDa subunit family. (270 aa) | ||||
Q5KF63_CRYNJ | 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. (121 aa) | ||||
Q5KF78_CRYNJ | Negative regulation of transcription by glucose-related protein, putative. (275 aa) | ||||
Q5KFA1_CRYNJ | 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. (270 aa) | ||||
Q5KFB9_CRYNJ | ATP synthase subunit alpha; Produces ATP from ADP in the presence of a proton gradient across the membrane. (540 aa) | ||||
Q5KFE4_CRYNJ | Uncharacterized protein. (663 aa) | ||||
Q5KFF8_CRYNJ | 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. (119 aa) | ||||
Q5KFH7_CRYNJ | t-SNARE coiled-coil homology domain-containing protein. (392 aa) | ||||
Q5KFL3_CRYNJ | NAD_binding_2 domain-containing protein. (312 aa) | ||||
Q5KFL5_CRYNJ | Cytochrome c oxidase subunit; This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport. (82 aa) | ||||
Q5KFS7_CRYNJ | AP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (220 aa) | ||||
Q5KFT4_CRYNJ | Electron transporter, transferring electrons within CoQH2-cytochrome c reductase complex, putative. (320 aa) | ||||
Q5KFU0_CRYNJ | ATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (547 aa) | ||||
Q5KFX3_CRYNJ | UAS domain-containing protein. (567 aa) | ||||
Q5KG39_CRYNJ | J domain-containing protein. (615 aa) | ||||
Q5KG89_CRYNJ | Heterotrimeric G-protein GTPase, putative. (358 aa) | ||||
Q5KGB2_CRYNJ | AP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (164 aa) | ||||
Q5KGD9_CRYNJ | 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. (144 aa) | ||||
Q5KGN1_CRYNJ | Ubiquitin conjugating enzyme, putative; Belongs to the ubiquitin-conjugating enzyme family. (175 aa) | ||||
Q5KGP7_CRYNJ | Oxidored_q6 domain-containing protein; Belongs to the complex I 20 kDa subunit family. (229 aa) | ||||
Q5KGU5_CRYNJ | Cytochrome b-c1 complex subunit Rieske, mitochondrial; Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis. (279 aa) | ||||
Q5KGV5_CRYNJ | Endodeoxyribonuclease, putative. (618 aa) | ||||
Q5KGZ9_CRYNJ | ATP binding protein, putative; Belongs to the STXBP/unc-18/SEC1 family. (672 aa) | ||||
Q5KH01_CRYNJ | Polyphosphoinositide phosphatase, putative. (827 aa) | ||||
Q5KH85_CRYNJ | 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. (939 aa) | ||||
Q5KHA1_CRYNJ | ATP synthase subunit gamma. (288 aa) | ||||
Q5KHC9_CRYNJ | Expressed protein. (325 aa) | ||||
Q5KHT1_CRYNJ | Protein-Golgi retention-related protein, putative. (295 aa) | ||||
Q5KHT8_CRYNJ | Expressed protein. (314 aa) | ||||
Q5KHU7_CRYNJ | 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. (259 aa) | ||||
Q5KHW4_CRYNJ | Mitochondrial import inner membrane translocase subunit tim23, putative. (241 aa) | ||||
Q5KI28_CRYNJ | Ubiquinol-cytochrome-c reductase, putative. (166 aa) | ||||
Q5KI75_CRYNJ | 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. (921 aa) | ||||
Q5KI86_CRYNJ | WD_REPEATS_REGION domain-containing protein. (343 aa) | ||||
Q5KIA5_CRYNJ | Uncharacterized protein. (1021 aa) | ||||
Q5KID6_CRYNJ | 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. (306 aa) | ||||
Q5KID7_CRYNJ | 1-phosphatidylinositol-3-phosphate 5-kinase, putative. (2432 aa) | ||||
Q5KID8_CRYNJ | Uncharacterized protein. (2102 aa) | ||||
Q5KIE2_CRYNJ | Uncharacterized protein. (208 aa) | ||||
Q5KIF5_CRYNJ | Uncharacterized protein; Belongs to the synaptobrevin family. (224 aa) | ||||
Q5KIM9_CRYNJ | Uncharacterized protein. (106 aa) | ||||
Q5KIN5_CRYNJ | 1-acyl-sn-glycerol-3-phosphate acyltransferase; Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family. (783 aa) | ||||
Q5KIN6_CRYNJ | V-type proton ATPase subunit a; Essential component of the vacuolar proton pump (V-ATPase), a multimeric enzyme that catalyzes the translocation of protons across the membranes. Required for assembly and activity of the V-ATPase. (849 aa) | ||||
Q5KIV8_CRYNJ | t-SNARE coiled-coil homology domain-containing protein. (257 aa) | ||||
Q5KIW2_CRYNJ | Uncharacterized protein. (250 aa) | ||||
Q5KIZ0_CRYNJ | Uncharacterized protein. (61 aa) | ||||
Q5KIZ1_CRYNJ | Dolichyl-phosphate-mannose-protein mannosyltransferase, putative. (767 aa) | ||||
Q5KIZ7_CRYNJ | Uncharacterized protein. (122 aa) | ||||
Q5KJ79_CRYNJ | Expressed protein. (73 aa) | ||||
Q5KJC6_CRYNJ | Uncharacterized protein. (697 aa) | ||||
Q5KJD9_CRYNJ | Expressed protein. (385 aa) | ||||
Q5KJG1_CRYNJ | 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. (396 aa) | ||||
Q5KJI7_CRYNJ | Golgi to vacuole transport-related protein, putative. (849 aa) | ||||
Q5KJJ6_CRYNJ | BET1 protein, putative. (155 aa) | ||||
Q5KJJ9_CRYNJ | Cytoplasm protein, putative. (654 aa) | ||||
Q5KJP2_CRYNJ | Voltage-dependent ion-selective channel, putative. (292 aa) | ||||
Q5KJQ3_CRYNJ | Expressed protein. (60 aa) | ||||
Q5KJQ5_CRYNJ | High-affinity iron permease CaFTR1, putative. (433 aa) | ||||
Q5KJQ6_CRYNJ | Ferroxidase, putative; Belongs to the multicopper oxidase family. (639 aa) | ||||
Q5KJT0_CRYNJ | X15341 cytochrome C oxidase subunit, putative; Belongs to the cytochrome c oxidase subunit 6A family. (119 aa) | ||||
Q5KJT1_CRYNJ | J domain-containing protein. (717 aa) | ||||
Q5KJV2_CRYNJ | Hydrogen-transporting ATP synthase, putative. (100 aa) | ||||
Q5KJW3_CRYNJ | Uncharacterized protein. (121 aa) | ||||
Q5KJZ1_CRYNJ | Mitochondrial inner membrane protease subunit. (222 aa) | ||||
Q5KK05_CRYNJ | 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 [...] (297 aa) | ||||
Q5KK91_CRYNJ | Uncharacterized protein. (156 aa) | ||||
Q5KKE9_CRYNJ | Vacuolar protein sorting-associated protein 35; Plays a role in vesicular protein sorting. (938 aa) | ||||
Q5KKG9_CRYNJ | Signal recognition particle binding protein, putative. (674 aa) | ||||
Q5KKI3_CRYNJ | Uncharacterized protein. (119 aa) | ||||
Q5KKK1_CRYNJ | Uncharacterized protein. (532 aa) | ||||
Q5KKS9_CRYNJ | ATP-dependent peptidase, putative. (782 aa) | ||||
Q5KKW7_CRYNJ | Uncharacterized protein. (175 aa) | ||||
Q5KKX0_CRYNJ | Expressed protein. (302 aa) | ||||
Q5KL04_CRYNJ | DigA protein, putative. (1177 aa) | ||||
Q5KL26_CRYNJ | ATP synthase, putative. (237 aa) | ||||
Q5KL41_CRYNJ | Expressed protein. (347 aa) | ||||
Q5KL66_CRYNJ | Vacuolar ATP synthase subunit d, putative. (263 aa) | ||||
Q5KLD3_CRYNJ | 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. (223 aa) | ||||
Q5KLE1_CRYNJ | Dolichyl-diphosphooligosaccharide-protein glycotransferase, putative. (322 aa) | ||||
Q5KLE4_CRYNJ | 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. (829 aa) | ||||
Q5KLI4_CRYNJ | ATPase, putative. (817 aa) | ||||
Q5KLP2_CRYNJ | 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) | ||||
Q5KLS9_CRYNJ | Mitochondrial import receptor subunit tom40, putative. (375 aa) | ||||
Q5KLT1_CRYNJ | 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. (696 aa) | ||||
Q5KLT4_CRYNJ | Peptidase, putative. (182 aa) | ||||
Q5KLY0_CRYNJ | Adaptor complex subunit medium chain 3, putative; Belongs to the adaptor complexes medium subunit family. (454 aa) | ||||
Q5KLZ6_CRYNJ | Cytochrome-c oxidase chain VI, putative. (142 aa) | ||||
Q5KM37_CRYNJ | Phosphatidylinositol 3-kinase VPS34. (880 aa) | ||||
Q5KPZ9_CRYNJ | MCU domain-containing protein. (556 aa) | ||||
Q5KM59_CRYNJ | Expressed protein. (395 aa) | ||||
Q5KMF5_CRYNJ | Intracellular protein transport-related protein, putative; Belongs to the adaptor complexes medium subunit family. (428 aa) | ||||
Q5KMH4_CRYNJ | Protein kinase/endoribonuclease, putative. (1073 aa) | ||||
Q5KMJ1_CRYNJ | t-SNARE, putative; Belongs to the syntaxin family. (274 aa) | ||||
Q5KMK2_CRYNJ | Expressed protein. (379 aa) | ||||
Q5KMN4_CRYNJ | Ion_trans domain-containing protein. (554 aa) | ||||
Q5KMQ0_CRYNJ | Uncharacterized protein. (335 aa) | ||||
Q5KMR1_CRYNJ | Succinate dehydrogenase [ubiquinone] cytochrome b small subunit. (181 aa) | ||||
Q5KMR4_CRYNJ | Uncharacterized protein. (835 aa) | ||||
Q5KMS5_CRYNJ | Probable vacuolar protein sorting-associated protein 16 homolog; Essential for vacuolar protein sorting. Required for vacuole biogenesis, stability and to maintain vacuole morphology. (847 aa) | ||||
Q5KMV9_CRYNJ | ATP synthase delta chain, mitochondrial, putative. (168 aa) | ||||
Q5KMY1_CRYNJ | Protein-vacuolar targeting-related protein, putative. (187 aa) | ||||
Q5KMZ4_CRYNJ | Ligase, putative. (852 aa) | ||||
Q5KN99_CRYNJ | Alpha-1,6-mannosyltransferase, putative. (572 aa) | ||||
Q5KNA1_CRYNJ | Serine C-palmitoyltransferase, putative. (526 aa) | ||||
Q5KNC8_CRYNJ | Uncharacterized protein. (80 aa) | ||||
Q5KND0_CRYNJ | 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. (444 aa) | ||||
Q5KNG8_CRYNJ | 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. (213 aa) | ||||
Q5KPS8_CRYNJ | Heterotrimeric G protein alpha subunit B, putative. (352 aa) | ||||
Q5KNJ1_CRYNJ | ATP-binding cassette (ABC) transporter, putative. (853 aa) | ||||
Q5KNL8_CRYNJ | Uncharacterized protein. (283 aa) | ||||
Q5KNR5_CRYNJ | Uncharacterized protein. (131 aa) | ||||
Q5KNT0_CRYNJ | Vacuolar ATP synthase subunit e, putative. (227 aa) | ||||
Q5KNV4_CRYNJ | Expressed protein. (85 aa) | ||||
Q5KNV6_CRYNJ | Expressed protein. (76 aa) | ||||
Q5KNY1_CRYNJ | Retrograde transport, endosome to Golgi-related protein, putative. (817 aa) | ||||
Q5KP16_CRYNJ | 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 [...] (123 aa) | ||||
Q5KP19_CRYNJ | Protein-vacuolar targeting-related protein, putative. (202 aa) | ||||
Q5KP23_CRYNJ | DUF1681 domain-containing protein. (200 aa) | ||||
Q5KP39_CRYNJ | V-type proton ATPase subunit; 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; Belongs to the V-ATPase V0D/AC39 subunit family. (356 aa) | ||||
Q5KP61_CRYNJ | Late endosome to vacuole transport-related protein, putative. (212 aa) | ||||
Q5KP79_CRYNJ | Cell division cycle protein 91, putative. (436 aa) | ||||
Q5KPA4_CRYNJ | Succinate dehydrogenase (Ubiquinone), putative. (177 aa) | ||||
Q5KPD4_CRYNJ | 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. (294 aa) | ||||
Q5KQ15_CRYNJ | Conserved expressed protein. (547 aa) | ||||
Q5KPE2_CRYNJ | Uncharacterized protein. (159 aa) | ||||
Q5KPF8_CRYNJ | Protein transport protein BOS1; SNARE required for protein transport between the ER and the Golgi complex. (241 aa) | ||||
Q5KPI4_CRYNJ | V-type proton ATPase 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. (164 aa) | ||||
Q5KPJ0_CRYNJ | NAD_binding_2 domain-containing protein. (318 aa) | ||||
Q5KPL4_CRYNJ | GLUE N-terminal domain-containing protein. (545 aa) | ||||
Q5KPM7_CRYNJ | Chaperone, putative. (103 aa) |