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ACB00269.1 | Conserved hypothetical protein; Similar to alr3388 of Nostoc sp. PCC 7120. (99 aa) | ||||
ndhD | NADH dehydrogenase subunit 4; NDH-1 shuttles electrons from NAD(P)H, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient; Belongs to the complex I subunit 4 family. (550 aa) | ||||
petJ-2 | Cytochrome c6; Similar to all0161 of Nostoc sp. strain PCC 7120. (115 aa) | ||||
psaL | Photosystem I reaction center subunit XI. (152 aa) | ||||
psaK | Photosystem I reaction center subunit X; Similar to ssr0390 of Synechocystis sp. PCC 6803. (87 aa) | ||||
sufA-2 | Iron transport protein; Similar to slr1295 of Synechocystis sp. PCC 6803. (363 aa) | ||||
psbZ-2 | Photosystem II 11 kD protein; Plays a role in the repair and/or biogenesis of the calcium- manganese-oxide cluster on the lumenal face of the thylakoid membrane. Its presence in a photosystem II (PSII) preparation prevents binding of some small extrinsic subunits and thus assembly of calcium-manganese- oxide cluster. (137 aa) | ||||
ndhH | NADH dehydrogenase subunit H; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (394 aa) | ||||
ndhB | NADH dehydrogenase subunit B; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (526 aa) | ||||
ACB00596.1 | Conserved hypothetical protein (DUF477). (232 aa) | ||||
ftsH-2 | ATP-dependent metalloprotease FtsH subfamily; Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins; Belongs to the AAA ATPase family. In the central section; belongs to the AAA ATPase family. (620 aa) | ||||
ACA98067.1 | Conserved hypothetical protein; Similar to slr1949 of Synechocystis sp. PCC 6803. (217 aa) | ||||
ACA98095.1 | Conserved hypothetical protein; Similar to sll0982 of Synechocystis sp. PCC 6803. (129 aa) | ||||
psbV | Cytochrome c-550 precursor (Cytochrome c550) (Low potential cytochrome c550); Low-potential cytochrome c that plays a role in the oxygen- evolving complex of photosystem II. (170 aa) | ||||
psbZ | Photosystem II subunit PsbZ; Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna; Belongs to the PsbZ family. (62 aa) | ||||
psbA-II | Photosystem II D1 subunit PsbA-II (Qb protein); Similar to slr1311 of Synechocystis sp. PCC 6803. (348 aa) | ||||
petJ | Cytochrome c6 precursor (Cytochrome c553); Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis. (117 aa) | ||||
psbE | Cytochrome b559, alpha subunit (Photosystem II subunit PsbE); 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. (81 aa) | ||||
psbF | Cytochrome b559, beta subunit (Photosystem II subunit PsbF); 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 subunit PsbL; 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. (39 aa) | ||||
psbJ | Photosystem II subunit PsbJ; This protein is a component of the reaction center of photosystem II; Belongs to the PsbJ family. (39 aa) | ||||
psbO | Photosystem II manganese stabilizing protein PsbO; Similar to sll0427 of Synechocystis sp. PCC 6803. (278 aa) | ||||
psbU | Photosystem II 12 kDa extrinsic protein (PsbU); Stabilizes the structure of photosystem II oxygen-evolving complex (OEC), the ion environment of oxygen evolution and protects the OEC against heat-induced inactivation. (138 aa) | ||||
petG | Cytochrome b6-f complex subunit 5; 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. PetG is required for either the stability or assembly of the cytochrome b6-f complex. (38 aa) | ||||
ACA98463.1 | Conserved hypothetical protein; Similar to sll1769 of Synechocystis sp. PCC 6803. (113 aa) | ||||
ACA98480.1 | Conserved hypothetical protein; Similar to slr1513 of Synechocystis sp. PCC 6803. (104 aa) | ||||
ndhL | NADH dehydrogenase subunit L (inorganic carbon tranpsort protein); NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (77 aa) | ||||
ndhM | Conserved hypothetical protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (119 aa) | ||||
cpcG | Phycocyanin-associated phycobilisome rod-core linker polypeptide; Similar to sll1471 of Synechocystis sp. PCC6803; Belongs to the phycobilisome linker protein family. (242 aa) | ||||
thf1 | Conserved hypothetical protein; May be involved in photosynthetic membrane biogenesis. (254 aa) | ||||
atpG | ATP synthase F1, gamma subunit; Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex. (314 aa) | ||||
atpA | ATP synthase F1, alpha subunit; 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. (505 aa) | ||||
atpH | ATP synthase F1, delta subunit; 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. (185 aa) | ||||
atpF | ATP synthase B chain (Subunit I); 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. (175 aa) | ||||
atpG-2 | ATP synthase B chain (Subunit II); 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. (161 aa) | ||||
atpE | ATP synthase C chain (Lipid-binding protein); 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. (81 aa) | ||||
atpB | ATP synthase F0, A subunit; Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane. (244 aa) | ||||
atpD | ATP synthase beta chain; 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. (483 aa) | ||||
atpC | ATP synthase F1, epsilon subunit; Produces ATP from ADP in the presence of a proton gradient across the membrane. (134 aa) | ||||
psbH | Phosphoprotein of photosystem II; 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. (67 aa) | ||||
psbN | Photosystem II reaction center N protein.-related protein; May play a role in photosystem I and II biogenesis. Belongs to the PsbN family. (43 aa) | ||||
cpcG-2 | Phycobilisome rod-core linker polypeptide cpcG (L-RC 28.5); Rod-core linker protein required for attachment of phycocyanin to allophycocyanin in cores of phycobilisomes. (248 aa) | ||||
petD | Cytb6/f complex subunit IV; 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. (160 aa) | ||||
petB | Cytochrome b6; 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. (222 aa) | ||||
ctpA | Carboxyl-terminal protease; Cleavage of the 16 C-terminal residues from the D1 precursor of photosystem II (PSII). This proteolytic processing is necessary to allow the light-driven assembly of the oxygen-evolving cluster (a tetranuclear manganese), which is responsible for photosynthetic water oxidation. (414 aa) | ||||
petH | ferredoxin-NADP reductase; Similar to gene slr1643 of Synechocystis sp. PCC 6803. (402 aa) | ||||
ftsH-4 | Cell division protein ftsH like protein (ATP-dependent zinc metallopeptidase); Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins; Belongs to the AAA ATPase family. In the central section; belongs to the AAA ATPase family. (625 aa) | ||||
ndhE | NADH dehydrogenase subunit E; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (103 aa) | ||||
ndhI | NADH-plastoquinone oxidoreductase, I subunit; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient (By similarity); Belongs to the complex I 23 kDa subunit family. (203 aa) | ||||
ndhA | NADH dehydrogenase subunit A; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. (372 aa) | ||||
psbT | Photosystem II reaction center, PsbT protein; Seems to play a role in the dimerization of PSII. Belongs to the PsbT family. (31 aa) | ||||
ycf12 | Conserved hypothetical protein Ycf12; A core subunit of photosystem II (PSII); Belongs to the Ycf12 family. (43 aa) | ||||
psaJ | Photosystem I reaction centre, subunit IX / PsaJ; May help in the organization of the PsaE and PsaF subunits. Belongs to the PsaJ family. (37 aa) | ||||
secE | Preprotein translocase, SecE subunit; Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation. (75 aa) | ||||
secY | Preprotein translocase SecY subunit; The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently. (439 aa) | ||||
ccs1 | C-type cytochrome biogenesis protein; Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment. (462 aa) | ||||
ycf4 | Photosystem I assembly protein ycf4; Seems to be required for the assembly of the photosystem I complex; Belongs to the Ycf4 family. (188 aa) | ||||
ndhN | Conserved hypothetical protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (157 aa) | ||||
ssb-2 | Single-stranded DNA-binding protein; Similar to slr1034 in Synechocystis sp. PCC 6803. (148 aa) | ||||
ftsH | Cell division protein; Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins; Belongs to the AAA ATPase family. In the central section; belongs to the AAA ATPase family. (637 aa) | ||||
psbW | Photosystem II reaction center W protein; Similar to sll1398 in Synechocystis sp. PCC 6803; Belongs to the Psb28 family. (111 aa) | ||||
secA | Preprotein translocase, SecA subunit; Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane; Belongs to the SecA family. (938 aa) | ||||
isiA | Photosystem II chlorophyll-binding protein; Functions as an antenna for photosystem I (PSI) under iron- limiting conditions, when phycobilisomes disappear. In the (PSI)3(Isi3)18 complex most of the harvested energy is probably used by PSI; in other PSI-containing supercomplexes a large part of the energy will probably not be used for light harvesting, but rather is dissipated to protect the organism from light damage. Belongs to the PsbB/PsbC family. IsiA/Pcb subfamily. (284 aa) | ||||
psbY | Photosystem II PsbY protein; Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II. Belongs to the PsbY family. (38 aa) | ||||
psaE | Photosystem I reaction center subunit IV; Stabilizes the interaction between PsaC and the PSI core, assists the docking of the ferredoxin to PSI and interacts with ferredoxin-NADP oxidoreductase; Belongs to the PsaE family. (70 aa) | ||||
psbA | Photosystem q(b) 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. (360 aa) | ||||
psbC | Photosystem II 44 kDa subunit reaction center protein; One of the components of the core complex of photosystem II (PSII). It binds chlorophyll and helps catalyze the primary light- induced photochemical processes of PSII. PSII is a light-driven water:plastoquinone oxidoreductase, using light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation; Belongs to the PsbB/PsbC family. PsbC subfamily. (469 aa) | ||||
psbD | Photosystem II D2 protein (photosystem q(a) 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 s [...] (352 aa) | ||||
ycf3 | Photosystem I assembly protein ycf3; Essential for the assembly of the photosystem I (PSI) complex. May act as a chaperone-like factor to guide the assembly of the PSI subunits; Belongs to the Ycf3 family. (173 aa) | ||||
psaC | Photosystem I iron-sulfur center subunit VII; 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 character [...] (81 aa) | ||||
ACA99595.1 | Conserved hypothetical protein; Similar to sll1638 in Synechocystis sp. PCC 6803. (152 aa) | ||||
apcF | Allophycocyanin beta-18 subunit; A variant beta-allophycocyanin (AP) which forms a complex with ApcE, a phycobilisome terminal emitter that influences energy transfer to photosystem II; Belongs to the phycobiliprotein family. (169 aa) | ||||
ACA99677.1 | Conserved hypothetical protein; Similar to ssl2009 in Synechocystis sp. PCC 6803. (100 aa) | ||||
psbB | Photosystem II protein; One of the components of the core complex of photosystem II (PSII). It binds chlorophyll and helps catalyze the primary light- induced photochemical processes of PSII. PSII is a light-driven water:plastoquinone oxidoreductase, using light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation; Belongs to the PsbB/PsbC family. PsbB subfamily. (507 aa) | ||||
psaM | Similar to asr4657 of Nostoc sp. PCC 7120. (31 aa) | ||||
ACB00779.1 | Carotenoid binding protein; Similar to slr1963 of Synechocystis sp. PCC 6803; Belongs to the orange carotenoid-binding protein family. (320 aa) | ||||
ACB00777.1 | Conserved hypothetical protein; Similar to slr1964 of Synechocystis sp. PCC 6803. (111 aa) | ||||
ACB00764.1 | S4 domain protein; Similar to alr2890 of Nostoc sp. PCC 7120. (253 aa) | ||||
psbK | Photosystem II 4 kDa reaction center component superfamily; 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. (45 aa) | ||||
ACB00725.1 | Conserved hypothetical protein; Similar to sll0997 of Synechocystis sp. PCC 6803. (307 aa) | ||||
ndhJ | NADH dehydrogenase subunit J; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (174 aa) | ||||
ndhK | NADH dehydrogenase subunit K; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration; Belongs to the complex I 20 kDa subunit family. (243 aa) | ||||
ndhC | NADH dehydrogenase subunit C; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (120 aa) | ||||
ACB00671.1 | Conserved hypothetical protein; Similar to slr1796 of Synechocystis sp. PCC 6803. (189 aa) | ||||
psaI | Photosystem I reaction center subunit VIII; May help in the organization of the PsaL subunit. Belongs to the PsaI family. (38 aa) | ||||
petC | Rieske FeS protein; 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. Belongs to the Rieske iron-sulfur protein family. (180 aa) | ||||
petA | Apocytochrome f precursor; 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. (325 aa) | ||||
ccsA | C-type cytochrome synthesis protein; Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment. (338 aa) | ||||
apcC | Allophycocyanin-associated phycobilisome 7.8-kDa core-linker polypeptide; Rod linker protein, associated with allophycocyanin. Linker polypeptides determine the state of aggregation and the location of the disk-shaped phycobiliprotein units within the phycobilisome and modulate their spectroscopic properties in order to mediate a directed and optimal energy transfer. (67 aa) | ||||
apcB | Allophycocyanin, beta subunit; Light-harvesting photosynthetic bile pigment-protein from the phycobiliprotein complex. Allophycocyanin has a maximum absorption at approximately 650 nanometers. (161 aa) | ||||
apcA | Allophycocyanin alpha subunit; Light-harvesting photosynthetic bile pigment-protein from the phycobiliprotein complex. Allophycocyanin has a maximum absorption at approximately 650 nanometers (By similarity). (161 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. (739 aa) | ||||
psaB | Photosystem I protein 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) | ||||
ndhD2 | NADH dehydrogenase subunit D2; NDH-1 shuttles electrons from NAD(P)H, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient; Belongs to the complex I subunit 4 family. (534 aa) | ||||
ndhD1 | NADH dehydrogenase subunit D1; NDH-1 shuttles electrons from NAD(P)H, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient; Belongs to the complex I subunit 4 family. (526 aa) | ||||
apcE | Phycobilisome core-membrane linker phycobiliprotein ApcE; This protein is postulated to act both as terminal energy acceptor (by its phycobilin-like domains) and as a linker polypeptide (by its repeats and arms) that stabilizes the phycobilisome core architecture (By similarity). Has intrinsic bilin lyase activity. (886 aa) | ||||
ACB00074.1 | Conserved hypothetical protein (DUF362); Similar to alr3725 of Nostoc sp. PCC 7120. (319 aa) | ||||
ndhO | Conserved hypothetical protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. (71 aa) | ||||
apcD | Allophycocyanin B alpha subunit; A variant alpha-allophycocyanin (AP) which forms a complex with beta-AP with maximum absorption at approximately 670 nanometers. It is an important phycobilisome terminal emitter involved in energy transfer to photosystem I (By similarity); Belongs to the phycobiliprotein family. (161 aa) | ||||
psbM | Photosystem II reaction centre M protein; 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. (34 aa) | ||||
psbA-2 | Photosystem q(b) 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. (360 aa) | ||||
psbD-2 | Photosystem II D2 protein. (352 aa) | ||||
cpcB | Phycocyanin, beta subunit; Light-harvesting photosynthetic bile pigment-protein from the phycobiliprotein complex. (172 aa) | ||||
cpcA | Phycocyanin, alpha subunit; Light-harvesting photosynthetic bile pigment-protein from the phycobiliprotein complex. (162 aa) | ||||
cpcC | Phycocyanin-associated rod linker protein; Rod linker protein, associated with phycocyanin. Linker polypeptides determine the state of aggregation and the location of the disk-shaped phycobiliprotein units within the phycobilisome and modulate their spectroscopic properties in order to mediate a directed and optimal energy transfer. (290 aa) | ||||
cpcD | Phycocyanin-associated, rod-terminating linker protein CpcD; Rod linker protein, associated with phycocyanin. Linker polypeptides determine the state of aggregation and the location of the disk-shaped phycobiliprotein units within the phycobilisome and modulate their spectroscopic properties in order to mediate a directed and optimal energy transfer. (80 aa) |