Your Input: | |
| | B8LCN4_THAPS | Predicted protein. (414 aa) |
| | B8LCT5_THAPS | 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) |
| | B8LCU5_THAPS | Phosphatidylinositol 3-kinase; Belongs to the PI3/PI4-kinase family. (258 aa) |
| | PETC2 | Cytochrome b6-f complex iron-sulfur subunit; Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions. (181 aa) |
| | B8LD94_THAPS | Predicted protein. (105 aa) |
| | B8LDE7_THAPS | Predicted protein. (72 aa) |
| | B8LDI9_THAPS | Sar1-type small G protein; Belongs to the small GTPase superfamily. SAR1 family. (194 aa) |
| | Lhcr8 | Fucoxanthin chl a/c light-harvesting protein. (222 aa) |
| | B8LDW8_THAPS | Cytochrome c1. (277 aa) |
| | B8LDX7_THAPS | H-atpase subunit alpha. (322 aa) |
| | B8LE06_THAPS | Sec1-family transport protein; Belongs to the STXBP/unc-18/SEC1 family. (457 aa) |
| | B8LE52_THAPS | Copia-like retroelement pol polyprotein found-like protein. (187 aa) |
| | B8LE78_THAPS | Predicted protein. (179 aa) |
| | B8LEL7_THAPS | Predicted protein. (624 aa) |
| | PSAE | PSAE, photosystem I reaction center subunit. (63 aa) |
| | B8LEQ9_THAPS | Predicted protein. (66 aa) |
| | atpA-3 | ATP synthase subunit alpha; Produces ATP from ADP in the presence of a proton gradient across the membrane. (503 aa) |
| | atpD-2 | Plastid thylakoid ATPase delta chain, plastid protein. (187 aa) |
| | atpF-2 | Plastid thylakoid ATPase subunit, plastid protein; Belongs to the ATPase B chain family. (179 aa) |
| | B8LER4_THAPS | Predicted protein; Belongs to the ATPase B chain family. (156 aa) |
| | B8LER5_THAPS | Predicted protein; Belongs to the ATPase C chain family. (82 aa) |
| | PsbV | Cytochrome c550, PsbV. (163 aa) |
| | B8LES4_THAPS | Predicted protein. (733 aa) |
| | B8LET6_THAPS | ATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (474 aa) |
| | B8LEU4_THAPS | Predicted protein. (181 aa) |
| | B8LEU5_THAPS | Cytochrome b559 subunit alpha; This b-type cytochrome is tightly associated with the reaction center of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. (84 aa) |
| | PSAF | PSAF, photosystem I reaction center subunit. (169 aa) |
| | B8LEX2_THAPS | Tim17-like protein. (140 aa) |
| | B8LEY8_THAPS | SNARE component. (284 aa) |
| | atpC_2 | 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. (162 aa) |
| | B8BVG6_THAPS | Cytochrome b6-f complex iron-sulfur subunit; Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions. (212 aa) |
| | APM3 | Mu subunit of clathrin adaptor complex AP3; Belongs to the adaptor complexes medium subunit family. (427 aa) |
| | B8BWC2_THAPS | Uncharacterized protein. (178 aa) |
| | B8BWD3_THAPS | t-SNARE coiled-coil homology domain-containing protein. (492 aa) |
| | B8BWD4_THAPS | Uncharacterized protein. (1705 aa) |
| | B8BWF3_THAPS | Uncharacterized protein. (1058 aa) |
| | B8BWQ6_THAPS | Syntaxin, epimorphin family; Belongs to the syntaxin family. (265 aa) |
| | B8BWR3_THAPS | Uncharacterized protein. (1763 aa) |
| | B8BWT6_THAPS | NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12; 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. (244 aa) |
| | risp1 | 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. (168 aa) |
| | B8BX29_THAPS | Uncharacterized protein. (588 aa) |
| | STT3b | Oliosaccharyl transferase. (725 aa) |
| | B8BX97_THAPS | Uncharacterized protein. (174 aa) |
| | APM2 | Clathrin adaptor complex subunit; Belongs to the adaptor complexes medium subunit family. (426 aa) |
| | B8BXV1_THAPS | Uncharacterized protein. (258 aa) |
| | COP6 | 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. (303 aa) |
| | B8BY83_THAPS | TPR_REGION domain-containing protein. (200 aa) |
| | B8BY88_THAPS | Ion_trans domain-containing protein. (462 aa) |
| | SDH1 | 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). (240 aa) |
| | B8BYX3_THAPS | Uncharacterized protein. (612 aa) |
| | B8BZ96_THAPS | 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; Belongs to the SEC23/SEC24 family. SEC23 subfamily. (757 aa) |
| | B8BZJ7_THAPS | Uncharacterized protein. (230 aa) |
| | B8BZM1_THAPS | GrpE protein homolog; 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 GrpE family. (178 aa) |
| | B8BZP8_THAPS | DUF1681 domain-containing protein. (254 aa) |
| | B8C019_THAPS | Uncharacterized protein. (302 aa) |
| | COP2 | 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. (846 aa) |
| | THAPS_41256 | ATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (500 aa) |
| | THAPS_19298 | F-type H-ATPase delta subunit. (137 aa) |
| | B8BQH4_THAPS | Uncharacterized protein. (268 aa) |
| | B8BQK2_THAPS | ENTH domain-containing protein. (670 aa) |
| | B8BQQ2_THAPS | Uncharacterized protein. (1381 aa) |
| | B8BR47_THAPS | Uncharacterized protein. (644 aa) |
| | B8BR92_THAPS | V-type h-atpase subunit. (250 aa) |
| | B8BRG8_THAPS | Uncharacterized protein. (431 aa) |
| | APB3 | Beta subunit of clathrin adaptor protein AP3. (956 aa) |
| | B8BS51_THAPS | Mu subunit of AP4-like protein; Belongs to the adaptor complexes medium subunit family. (452 aa) |
| | B8BS55_THAPS | V-type h-atpase subunit; Belongs to the V-ATPase proteolipid subunit family. (191 aa) |
| | B8BS69_THAPS | Prohibitin. (258 aa) |
| | lhcx5 | Fucoxanthin chlorophyll a/c protein, LI818 clade. (236 aa) |
| | B8BSI6_THAPS | Uncharacterized protein. (72 aa) |
| | B8BTE1_THAPS | Uncharacterized protein. (1754 aa) |
| | B8BTK5_THAPS | Uncharacterized protein. (321 aa) |
| | B8BTR1_THAPS | Uncharacterized protein. (213 aa) |
| | VAT4 | 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. (166 aa) |
| | B8BTX3_THAPS | Peptidase_M6 domain-containing protein. (449 aa) |
| | B8BUA4_THAPS | Arf-type small G protein; Belongs to the small GTPase superfamily. SAR1 family. (192 aa) |
| | B8BUC5_THAPS | Uncharacterized protein. (853 aa) |
| | B8BUC7_THAPS | Ion_trans domain-containing protein. (354 aa) |
| | B8BUE6_THAPS | Uncharacterized protein. (208 aa) |
| | THAPS_29053 | 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. (329 aa) |
| | THAPS_23630 | Predicted protein. (437 aa) |
| | THAPS_35340 | Predicted protein. (182 aa) |
| | THAPS_35642 | Predicted protein. (61 aa) |
| | THAPS_35745 | Predicted protein. (243 aa) |
| | THAPS_596 | Predicted protein. (435 aa) |
| | THAPS_7044 | Predicted protein. (552 aa) |
| | THAPS_6974 | Predicted protein. (193 aa) |
| | THAPS_23464 | Predicted protein. (482 aa) |
| | THAPS_263135 | V-type H-ATPase subunit H. (299 aa) |
| | THAPS_6874 | Predicted protein. (640 aa) |
| | THAPS_23419 | Predicted protein. (1189 aa) |
| | THAPS_573 | 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. (162 aa) |
| | THAPS_23402 | Predicted protein. (243 aa) |
| | THAPS_23388 | Predicted protein. (324 aa) |
| | THAPS_38123 | Predicted protein. (280 aa) |
| | CYN | Cyanate hydratase; Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide; Belongs to the cyanase family. (205 aa) |
| | SEC61-1 | Protein translocase complex subunit; Belongs to the SecY/SEC61-alpha family. (473 aa) |
| | THAPS_38207 | Predicted protein. (72 aa) |
| | psb28 | Photosystem II reaction center Psb28 protein; Belongs to the Psb28 family. (114 aa) |
| | psaC | Photosystem I iron-sulfur center; Apoprotein for the two 4Fe-4S centers FA and FB of photosystem I (PSI); essential for photochemical activity. FB is the terminal electron acceptor of PSI, donating electrons to ferredoxin. The C-terminus interacts with PsaA/B/D and helps assemble the protein into the PSI complex. Required for binding of PsaD and PsaE to PSI. PSI is a plastocyanin/cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized accepto [...] (81 aa) |
| | psbA | Photosystem II protein D1; Photosystem II (PSII) is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1/D2 (PsbA/PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors. (360 aa) |
| | psbY-A | Photosystem II protein Y; Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II. Belongs to the PsbY family. (36 aa) |
| | psaJ | Photosystem I reaction center subunit IX; May help in the organization of the PsaE and PsaF subunits. Belongs to the PsaJ family. (41 aa) |
| | psaF | Photosystem I protein F. (185 aa) |
| | psbI | Photosystem II reaction center protein I; One of the components of the core complex of photosystem II (PSII), required for its stability and/or assembly. PSII is a light- driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. (38 aa) |
| | psaL | Photosystem I reaction center subunit XI. (148 aa) |
| | ycf4 | Photosystem I assembly protein Ycf4; Seems to be required for the assembly of the photosystem I complex; Belongs to the Ycf4 family. (181 aa) |
| | psbE | Cytochrome b559 subunit alpha; This b-type cytochrome is tightly associated with the reaction center of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. Belongs to the PsbE/PsbF family. (84 aa) |
| | psbF | Cytochrome b559 subunit beta; This b-type cytochrome is tightly associated with the reaction center of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. Belongs to the PsbE/PsbF family. (43 aa) |
| | psbL | Photosystem II reaction center protein L; One of the components of the core complex of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. This subunit is found at the monomer-monomer interface and is required for correct PSII assembly and/or dimerization. (38 aa) |
| | psbJ | Photosystem II reaction center protein J; One of the components of the core complex of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. (39 aa) |
| | psaD | Photosystem I ferredoxin-binding protein. (139 aa) |
| | psbZ | Photosystem II reaction center protein Z; Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna. (61 aa) |
| | ycf12 | Photosystem II reaction center protein Ycf12; A core subunit of photosystem II (PSII); Belongs to the Ycf12 family. (34 aa) |
| | psbD | Photosystem II D2 protein; Photosystem II (PSII) is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1/D2 (PsbA/PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors. D2 is needed for assembly of a stable PSII complex. (351 aa) |
| | psaI | Photosystem I reaction center subunit VIII; May help in the organization of the PsaL subunit. Belongs to the PsaI family. (36 aa) |
| | psbK | Photosystem II reaction center protein K; One of the components of the core complex of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. (44 aa) |
| | psaM | Photosystem I reaction center subunit XII. (30 aa) |
| | tatC | Sec-independent protein translocase component TatC. (246 aa) |
| | atpE | ATP synthase epsilon chain, chloroplastic; Produces ATP from ADP in the presence of a proton gradient across the membrane. (133 aa) |
| | atpB | ATP synthase subunit beta, chloroplastic; Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits; Belongs to the ATPase alpha/beta chains family. (474 aa) |
| | psaE | Photosystem I reaction center subunit IV. (65 aa) |
| | psbH | Photosystem II reaction center protein H; One of the components of the core complex of photosystem II (PSII), required for its stability and/or assembly. PSII is a light- driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. (66 aa) |
| | psbT | Photosystem II reaction center protein T; Seems to play a role in the dimerization of PSII. Belongs to the PsbT family. (32 aa) |
| | atpA | ATP synthase subunit alpha, chloroplastic; Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit. Belongs to the ATPase alpha/beta chains family. (503 aa) |
| | atpD | ATP synthase subunit delta, chloroplastic; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. 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 subunits to proton translocation; Belongs to the ATPase delta chain family. (187 aa) |
| | atpF | ATP synthase subunit b, chloroplastic; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. 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 subunits to proton translocation. (179 aa) |
| | atpG | ATP synthase subunit b', chloroplastic; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. 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 subunits to proton translocation. (156 aa) |
| | atpH | ATP synthase subunit c, chloroplastic; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. 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 subunits to proton translocation. (82 aa) |
| | atpI | ATP synthase subunit a, chloroplastic; Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane. (242 aa) |
| | psbX | Photosystem II reaction center X protein; Involved in the binding and/or turnover of quinones at the Q(B) site of Photosystem II. (38 aa) |
| | psbV | Cytochrome c-550; Low-potential cytochrome c that plays a role in the oxygen- evolving complex of photosystem II. (163 aa) |
| | B8C0F2_THAPS | Derlin; May be involved in the degradation of misfolded endoplasmic reticulum (ER) luminal proteins; Belongs to the derlin family. (164 aa) |
| | B8C0K7_THAPS | 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. (116 aa) |
| | VAT1 | Vacuolar proton pump subunit B; Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase; Belongs to the ATPase alpha/beta chains family. (506 aa) |
| | B8C0V0_THAPS | Cation channel. (393 aa) |
| | B8C0W4_THAPS | ATP synthase. (367 aa) |
| | COP3 | Coatomer protein subunit beta2. (1047 aa) |
| | B8C135_THAPS | ANK_REP_REGION domain-containing protein. (951 aa) |
| | B8C157_THAPS | V-snare protein, Vti1 C-terminal half-like protein. (116 aa) |
| | B8C193_THAPS | Uncharacterized protein. (321 aa) |
| | B8C1D2_THAPS | Uncharacterized protein. (120 aa) |
| | APB2 | Beta subunit of clathrin adaptor complex AP2. (853 aa) |
| | B8C1J4_THAPS | Uncharacterized protein. (296 aa) |
| | B8C1R6_THAPS | Uncharacterized protein. (282 aa) |
| | B8C1V5_THAPS | Uncharacterized protein. (81 aa) |
| | B8C2M1_THAPS | VPS37 C-terminal domain-containing protein. (381 aa) |
| | B8C2M2_THAPS | Uncharacterized protein. (616 aa) |
| | B8C2N9_THAPS | 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. (813 aa) |
| | B8C2P4_THAPS | Uncharacterized protein. (492 aa) |
| | B8C2S0_THAPS | Bac_surface_Ag domain-containing protein. (672 aa) |
| | B8C2T8_THAPS | DUF2012 domain-containing protein. (232 aa) |
| | B8C360_THAPS | V-type h-atpase subunit. (249 aa) |
| | B8C3S0_THAPS | Dnaj-like protein. (95 aa) |
| | B8C4A1_THAPS | Uncharacterized protein. (456 aa) |
| | B8C4C5_THAPS | Uncharacterized protein. (278 aa) |
| | SEC61-2 | Protein transportor; Belongs to the SecY/SEC61-alpha family. (479 aa) |
| | B8C4H8_THAPS | Uncharacterized protein; Belongs to the GrpE family. (253 aa) |
| | PsbO | Oxygen-evolving enhancer protein 1. (305 aa) |
| | B8C4L3_THAPS | Derlin; May be involved in the degradation of misfolded endoplasmic reticulum (ER) luminal proteins; Belongs to the derlin family. (220 aa) |
| | B8C5C9_THAPS | Uncharacterized protein. (683 aa) |
| | B8C5E5_THAPS | Uncharacterized protein. (803 aa) |
| | psaB | Photosystem I P700 chlorophyll a apoprotein A2; PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin/cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6. (733 aa) |
| | psaA | Photosystem I P700 chlorophyll a apoprotein A1; PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin/cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6. (752 aa) |
| | B8C5G1_THAPS | 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. (237 aa) |
| | B8C5G7_THAPS | APG6 domain-containing protein. (407 aa) |
| | B8C5I2_THAPS | Syntaxin. (295 aa) |
| | COP1 | 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. (1256 aa) |
| | B8C5Z0_THAPS | Uncharacterized protein. (87 aa) |
| | B8C646_THAPS | Uncharacterized protein. (206 aa) |
| | B8C650_THAPS | Derlin; May be involved in the degradation of misfolded endoplasmic reticulum (ER) luminal proteins; Belongs to the derlin family. (204 aa) |
| | atpA-2 | ATP synthase subunit alpha; Produces ATP from ADP in the presence of a proton gradient across the membrane. (542 aa) |
| | B8C6R8_THAPS | Putative v-type h-ATPase subunit. (212 aa) |
| | B8C704_THAPS | NADH dehydrogenase. (261 aa) |
| | Lhcr9 | Fucoxanthin chl a/c light-harvesting protein. (256 aa) |
| | B8C7T4_THAPS | Uncharacterized protein. (206 aa) |
| | B8C7V6_THAPS | Uncharacterized protein. (306 aa) |
| | APB1 | AP complex subunit beta. (920 aa) |
| | GPA1 | Heterotrimeric G protein alpha subunit 1. (357 aa) |
| | B8C8L2_THAPS | Synthase of ATP synthase. (209 aa) |
| | B8C8N0_THAPS | SNARE component. (283 aa) |
| | CHC | Clathrin heavy chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin heavy chain family. (1718 aa) |
| | APS2 | AP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (142 aa) |
| | B8C964_THAPS | Uncharacterized protein. (730 aa) |
| | B8C9G4_THAPS | APG6 domain-containing protein. (608 aa) |
| | B8C9G6_THAPS | Uncharacterized protein. (1332 aa) |
| | B8C9T9_THAPS | EMC1_C domain-containing protein. (1226 aa) |
| | B8CA52_THAPS | Uncharacterized protein. (611 aa) |
| | B8CA67_THAPS | Vacuolar protein sorting-associated protein 28 homolog; Component of the ESCRT-I complex (endosomal sorting complex required for transport I), a regulator of vesicular trafficking process. (225 aa) |
| | B8CA78_THAPS | Uncharacterized protein. (249 aa) |
| | B8CAM6_THAPS | Uncharacterized protein; Belongs to the PI3/PI4-kinase family. (571 aa) |
| | B8CAY2_THAPS | Adaptin_N domain-containing protein. (597 aa) |
| | B8CAY9_THAPS | Syntaxin, t-snare coiled-coil domain family. (418 aa) |
| | COP4 | 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. (908 aa) |
| | B8CBA1_THAPS | Alpha_adaptinC2 domain-containing protein. (927 aa) |
| | APA1 | Alpha subunit of tetrameric clathrin adaptor complex AP1. (927 aa) |
| | B8CBE6_THAPS | Derlin; May be involved in the degradation of misfolded endoplasmic reticulum (ER) luminal proteins; Belongs to the derlin family. (217 aa) |
| | B8CBG7_THAPS | NADH dehydrogenase [ubiquinone] flavoprotein 1, 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. (499 aa) |
| | B8CBP1_THAPS | Ubiquinol cytochrome c reductase. (78 aa) |
| | B8CBT0_THAPS | WD_REPEATS_REGION domain-containing protein. (337 aa) |
| | B8CBU3_THAPS | Signal recognition particle-like protein. (368 aa) |
| | VAT2 | Vacuolar proton pump alpha subunit. (621 aa) |
| | B8CC66_THAPS | Uncharacterized protein. (1490 aa) |
| | GPA2 | Heterotrimeric G protein alpha subunit 1. (336 aa) |
| | APG2 | AP-1 complex subunit gamma. (871 aa) |
| | VAT3 | V-type proton ATPase subunit; Subunit of the integral membrane V0 complex of vacuolar ATPase. 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. Belongs to the V-ATPase V0D/AC39 subunit family. (383 aa) |
| | B8CC85_THAPS | Coatomer COPII. (831 aa) |
| | B8CCA3_THAPS | Uncharacterized protein. (1481 aa) |
| | B8CCD5_THAPS | Tom40-like protein. (285 aa) |
| | B8CCG5_THAPS | Uncharacterized protein. (191 aa) |
| | B8CCG8_THAPS | Uncharacterized protein. (176 aa) |
| | B8BUF0_THAPS | Aminotran_1_2 domain-containing protein. (622 aa) |
| | B8BUF8_THAPS | t-SNARE coiled-coil homology domain-containing protein; Belongs to the syntaxin family. (395 aa) |
| | B8BUN5_THAPS | Uncharacterized protein. (486 aa) |
| | B8BUT9_THAPS | PsbP domain-containing protein. (261 aa) |
| | COP5 | 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. (514 aa) |
| | B8CCT7_THAPS | 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) |
| | APM1 | Mu subunit of tetrameric clathrin adaptor complex AP1; Belongs to the adaptor complexes medium subunit family. (442 aa) |
| | B8CCZ8_THAPS | Sec13-related protein; Belongs to the WD repeat SEC13 family. (304 aa) |
| | B8CD47_THAPS | Vps8 domain-containing protein. (752 aa) |
| | B8CD62_THAPS | Derlin; May be involved in the degradation of misfolded endoplasmic reticulum (ER) luminal proteins; Belongs to the derlin family. (294 aa) |
| | B8CDI7_THAPS | DUF1681 domain-containing protein. (270 aa) |
| | B8CDQ3_THAPS | V-type H+ transporting ATPase. (112 aa) |
| | B8CDS8_THAPS | Nadh-ubiquinone oxidoreductase. (319 aa) |
| | B8CDT6_THAPS | Uncharacterized protein. (698 aa) |
| | B8CE32_THAPS | DAO domain-containing protein. (431 aa) |
| | B8CES5_THAPS | Uncharacterized protein. (170 aa) |
| | B8CEY0_THAPS | Metallophos_2 domain-containing protein. (202 aa) |
| | B8CF97_THAPS | t-SNARE coiled-coil homology domain-containing protein. (459 aa) |
| | B8CFA2_THAPS | Tim23-like protein. (107 aa) |
| | B8CFC2_THAPS | t-SNARE coiled-coil homology domain-containing protein. (629 aa) |
| | B8CFD9_THAPS | Syntaxin. (92 aa) |
| | B8CFI9_THAPS | V-atpase subunit; Belongs to the V-ATPase proteolipid subunit family. (130 aa) |
| | B8CFQ4_THAPS | Peptidase_S24 domain-containing protein. (242 aa) |
| | B8CG98_THAPS | V-SNARE domain-containing protein. (214 aa) |
| | LASPO | L-aspartate oxidase. (570 aa) |
| | B8LC47_THAPS | Uncharacterized protein. (208 aa) |
| | B8LC69_THAPS | Predicted protein. (149 aa) |
| | B8LCD0_THAPS | Predicted protein. (1273 aa) |
