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| | EW14_0020 | Hypothetical protein; Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection. (116 aa) |
| | EW14_0035 | Serine--glyoxylate aminotransferase; Alternative locus ID: PMIT0604_0035. (378 aa) |
| | EW14_0047 | Replicative DNA helicase; Alternative locus ID: PMIT0604_0047. (298 aa) |
| | smc | Chromosome segregation ATPase; Required for chromosome condensation and partitioning. Belongs to the SMC family. (1194 aa) |
| | psbX | Photosystem II protein PsbX; Involved in the binding and/or turnover of quinones at the Q(B) site of Photosystem II. (61 aa) |
| | EW14_0097 | ATPase; Alternative locus ID: PMIT0604_0097. (429 aa) |
| | EW14_0132 | 6-pyruvoyl tetrahydrobiopterin synthase; Alternative locus ID: PMIT0604_0132. (308 aa) |
| | EW14_0140 | Oligoketide cyclase/lipid transport protein; Alternative locus ID: PMIT0604_0140. (156 aa) |
| | ndhO | 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. (78 aa) |
| | ycf3 | Photosystem I assembly related protein Ycf3; Seems to be required for the assembly of the photosystem I complex; Belongs to the Ycf3 family. (173 aa) |
| | ndhM | Putative subunit of NAD(P)H:quinone oxidoreductase; 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. (115 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. (534 aa) |
| | cugP | Putative sugar-phosphate nucleotidyl transferase; Catalyzes the formation of UDP-glucose, from UTP and glucose 1-phosphate. (392 aa) |
| | ndhE | NADH dehydrogenase subunit 4L; 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. (106 aa) |
| | ndhI | NAD(P)H-quinone oxidoreductase chain I; 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; Belongs to the complex I 23 kDa subunit family. (208 aa) |
| | ndhA | NAD(P)H-quinone oxidoreductase chain 1; 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) |
| | ndhH | NAD(P)H-quinone oxidoreductase chain 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. (395 aa) |
| | rplL | LSU ribosomal protein L7/L12 (P1/P2); Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation; Belongs to the bacterial ribosomal protein bL12 family. (131 aa) |
| | rplJ | LSU ribosomal protein L10p (P0); Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors. Belongs to the universal ribosomal protein uL10 family. (175 aa) |
| | rplA | LSU ribosomal protein L1p (L10Ae); Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release. (235 aa) |
| | rplK | LSU ribosomal protein L11p (L12e); Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. (141 aa) |
| | secE | Preprotein translocase subunit SecE; Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation. (80 aa) |
| | mutS2 | Recombination inhibitory protein MutS2; Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity; Belongs to the DNA mismatch repair MutS family. MutS2 subfamily. (803 aa) |
| | psbA | Photosystem II protein D1 (PsbA); 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) |
| | ftsH | Cell division protein FtsH; 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. (603 aa) |
| | EW14_0278 | DNA-3-methyladenine glycosylase II; Alternative locus ID: PMIT0604_0278; Belongs to the DNA glycosylase MPG family. (135 aa) |
| | EW14_0288 | Thymidylate synthase thyX; Catalyzes the reductive methylation of 2'-deoxyuridine-5'- monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor, and NADPH and FADH(2) as the reductant. (210 aa) |
| | psbH | Photosystem II 10 kDa phosphoprotein (PsbH); 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) |
| | psbN | Photosystem II protein PsbN; May play a role in photosystem I and II biogenesis. Belongs to the PsbN family. (58 aa) |
| | psbI | Photosystem II protein PsbI; 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. (42 aa) |
| | EW14_0304 | Hypothetical protein; Alternative locus ID: PMIT0604_0304; FIG00941574: hypothetical protein. (96 aa) |
| | psbK | Photosystem II protein PsbK; 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. (46 aa) |
| | EW14_0324 | Retinal pigment epithelial membrane protein; Alternative locus ID: PMIT0604_0324. (494 aa) |
| | EW14_0329 | Deoxyribodipyrimidine photolyase; Alternative locus ID: PMIT0604_0329; Belongs to the DNA photolyase family. (478 aa) |
| | ndhJ | NAD(P)H-quinone oxidoreductase chain 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. (176 aa) |
| | ndhK | NAD(P)H-quinone oxidoreductase chain 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. (244 aa) |
| | ndhC | NAD(P)H-quinone oxidoreductase subunit 3; 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) |
| | psbE | Cytochrome b559 alpha chain (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. (82 aa) |
| | psbF | Cytochrome b559 beta chain (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. (48 aa) |
| | psbJ | Photosystem II protein PsbJ; 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. (65 aa) |
| | EW14_0357 | SSU ribosomal protein S1p; Alternative locus ID: PMIT0604_0357. (363 aa) |
| | psbB | Photosystem II CP47 protein (PsbB); 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) |
| | psbM | Photosystem II protein PsbM; 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. (50 aa) |
| | EW14_0369 | dNTP triphosphohydrolase; Alternative locus ID: PMIT0604_0369; putative. (418 aa) |
| | petB | Cytochrome b6-f complex 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. (218 aa) |
| | petD | Cytochrome b6-f complex subunit IV (PetD); 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) |
| | psaE | Photosystem I subunit IV (PsaE); 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. (69 aa) |
| | EW14_0411 | Deoxyribodipyrimidine photolyase; Alternative locus ID: PMIT0604_0411; Belongs to the DNA photolyase family. (498 aa) |
| | recO | DNA recombination and repair protein RecO; Involved in DNA repair and RecF pathway recombination. (261 aa) |
| | rpsD | SSU ribosomal protein S4p (S9e); One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit. (188 aa) |
| | ndhB | NADH dehydrogenase subunit 2; 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. (506 aa) |
| | petA | Cytochrome b6-f complex 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. (322 aa) |
| | petC | Cytochrome b6-f complex iron-sulfur subunit PetC1; 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. (178 aa) |
| | psaJ | Photosystem I subunit IX (PsaJ); May help in the organization of the PsaE and PsaF subunits. Belongs to the PsaJ family. (44 aa) |
| | EW14_0512 | Photosystem I subunit III precursor; Alternative locus ID: PMIT0604_0512; plastocyanin (cyt c553) docking protein (PsaF). (184 aa) |
| | rplS | LSU ribosomal protein L19p; This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site. (156 aa) |
| | EW14_0536 | Pterin-4-alpha-carbinolamine dehydratase; Alternative locus ID: PMIT0604_0536. (96 aa) |
| | priA | Helicase PriA essential for oriC/DnaA-independent DNA replication; Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA; Belongs to the helicase family. PriA subfamily. (744 aa) |
| | EW14_0547 | Single-stranded DNA-binding protein; Alternative locus ID: PMIT0604_0547. (141 aa) |
| | psb27 | Photosystem II protein Psb27; 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. (104 aa) |
| | EW14_0575 | Hypothetical protein; Alternative locus ID: PMIT0604_0575; FIG00940617: hypothetical protein. (301 aa) |
| | EW14_0576 | SSU ribosomal protein S1p; Alternative locus ID: PMIT0604_0576. (401 aa) |
| | psaM | Putative photosystem I reaction centre subunit XII (PsaM); Alternative locus ID: PMIT0604_0586. (44 aa) |
| | chlL | Light-independent protochlorophyllide reductase iron-sulfur ATP-binding protein ChlL; Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The L component serves as a unique electron donor to the NB-component of the complex, and binds Mg-ATP. (295 aa) |
| | EW14_0593 | Hypothetical protein; Alternative locus ID: PMIT0604_0593; FIG00940838: hypothetical protein. (256 aa) |
| | EW14_0595 | Carboxysome shell protein CsoS1; Alternative locus ID: PMIT0604_0595. (103 aa) |
| | cbbL | Ribulose bisphosphate carboxylase large chain; RuBisCO catalyzes two reactions: the carboxylation of D- ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate in the photorespiration process. Both reactions occur simultaneously and in competition at the same active site. Belongs to the RuBisCO large chain family. Type I subfamily. (471 aa) |
| | EW14_0597 | Ribulose bisphosphate carboxylase small chain; Alternative locus ID: PMIT0604_0597. (113 aa) |
| | EW14_0599 | Carboxysome shell protein CsoS3; Alternative locus ID: PMIT0604_0599. (509 aa) |
| | EW14_0600 | Putative carboxysome peptide A; Alternative locus ID: PMIT0604_0600. (82 aa) |
| | EW14_0601 | Putative carboxysome peptide B; Alternative locus ID: PMIT0604_0601. (82 aa) |
| | EW14_0602 | Putative pterin-4 alpha-carbinolamine dehydratase-like protein; Alternative locus ID: PMIT0604_0602. (79 aa) |
| | EW14_0608 | N-acetyltransferase (GNAT) family; Alternative locus ID: PMIT0604_0608; Syn7942_0773 homolog, Ycf52 protein. (176 aa) |
| | EW14_0616 | NADH dehydrogenase subunit; Alternative locus ID: PMIT0604_0616; NdhL. (37 aa) |
| | EW14_0625 | Queuosine biosynthesis QueD; Alternative locus ID: PMIT0604_0625; PTPS-I. (156 aa) |
| | glmU | N-acetylglucosamine-1-phosphate uridyltransferase; Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP-GlcNAc). The C- terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N- acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5-monophosphate (from uridine 5- triphosphate), a reaction catalyzed by the N-terminal domain. (449 aa) |
| | EW14_0673 | Chlorophyll a/b-binding light-harvesting protein Pcb; Alternative locus ID: PMIT0604_0673. (352 aa) |
| | EW14_0755 | Hypothetical protein; Alternative locus ID: PMIT0604_0755; COG1565: Uncharacterized conserved protein. (396 aa) |
| | EW14_0800 | Cytochrome C553 (soluble cytochrome f); Alternative locus ID: PMIT0604_0800. (89 aa) |
| | EW14_0812 | mRNA 3-end processing factor; Alternative locus ID: PMIT0604_0812. (328 aa) |
| | thf1 | Hypothetical protein; May be involved in photosynthetic membrane biogenesis. (202 aa) |
| | ftsH-2 | FtsH ATP-dependent protease precursor; 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) |
| | rpsB | SSU ribosomal protein S2p (SAe); Alternative locus ID: PMIT0604_0842; Belongs to the universal ribosomal protein uS2 family. (234 aa) |
| | EW14_0855 | Cytochrome c-type bioproteinsis protein CcsA/ResC; Alternative locus ID: PMIT0604_0855. (221 aa) |
| | hemA | Glutamyl-tRNA reductase; Catalyzes the NADPH-dependent reduction of glutamyl-tRNA(Glu) to glutamate 1-semialdehyde (GSA). (405 aa) |
| | EW14_0859 | Glucose-1-phosphate adenylyltransferase; Alternative locus ID: PMIT0604_0859; Belongs to the bacterial/plant glucose-1-phosphate adenylyltransferase family. (428 aa) |
| | lpxD | UDP-3-O-(3-hydroxymyristoyl) glucosamine N-acyltransferase; Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3- hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell. Belongs to the transferase hexapeptide repeat family. LpxD subfamily. (344 aa) |
| | EW14_0886 | Thioredoxin family protein; Alternative locus ID: PMIT0604_0886. (182 aa) |
| | EW14_0928 | D-glycerate 3-kinase; Alternative locus ID: PMIT0604_0928; plant type. (314 aa) |
| | rpsO | SSU ribosomal protein S15p (S13e); Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome. (89 aa) |
| | dnaG | DNA primase; RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication. (676 aa) |
| | ispE | 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase; Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol. (311 aa) |
| | psb28 | Photosystem II 13 kDa protein Psb28 (PsbW); Alternative locus ID: PMIT0604_0965; Belongs to the Psb28 family. (117 aa) |
| | EW14_0972 | Serine--pyruvate aminotransferase; Alternative locus ID: PMIT0604_0972; L-alanine:glyoxylate aminotransferase. (394 aa) |
| | rpmB | LSU ribosomal protein L28p; Alternative locus ID: PMIT0604_0990; Belongs to the bacterial ribosomal protein bL28 family. (78 aa) |
| | rpmG | LSU ribosomal protein L33p; Alternative locus ID: PMIT0604_1023; Belongs to the bacterial ribosomal protein bL33 family. (64 aa) |
| | rpsR | SSU ribosomal protein S18p; Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit; Belongs to the bacterial ribosomal protein bS18 family. (73 aa) |
| | EW14_1032 | ATP-dependent Clp protease adaptor protein ClpS Cyano2; Alternative locus ID: PMIT0604_1032; Belongs to the ClpS family. (95 aa) |
| | ftsH-3 | Cell division protein FtsH; 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. (584 aa) |
| | rpmF | LSU ribosomal protein L32p; Alternative locus ID: PMIT0604_1050; Belongs to the bacterial ribosomal protein bL32 family. (57 aa) |
| | EW14_1079 | Hypothetical protein; Alternative locus ID: PMIT0604_1079; FIG017608: hypothetical membrane protein; specific for cyanobacteria. (212 aa) |
| | EW14_1139 | Hypothetical protein; Alternative locus ID: PMIT0604_1139; FIG00942471: hypothetical protein. (289 aa) |
| | petG | Cytochrome b6-f complex subunit V (PetG); 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. (49 aa) |
| | gyrA | DNA gyrase subunit A; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. (865 aa) |
| | EW14_1215 | Ferredoxin-NADP(+) reductase; Alternative locus ID: PMIT0604_1215. (375 aa) |
| | recR | Recombination protein RecR; May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO. (199 aa) |
| | psbY | Photosystem II protein PsbY; Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II. Belongs to the PsbY family. (43 aa) |
| | EW14_1322 | Hypothetical protein; Alternative locus ID: PMIT0604_1322; FIG00940651: hypothetical protein; Belongs to the SOS response-associated peptidase family. (212 aa) |
| | EW14_1352 | Selenoprotein O-like; Alternative locus ID: PMIT0604_1352. (567 aa) |
| | ycf4 | Photosystem I assembly related protein Ycf4; Seems to be required for the assembly of the photosystem I complex; Belongs to the Ycf4 family. (185 aa) |
| | psbD | Photosystem II protein D2 (PsbD); 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. (358 aa) |
| | psbC | Photosystem II CP43 protein (PsbC); 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. (460 aa) |
| | EW14_1408 | Ferric iron ABC transporter; Alternative locus ID: PMIT0604_1408; iron-binding protein. (340 aa) |
| | EW14_1416 | Hypothetical protein; Alternative locus ID: PMIT0604_1416; FIG00942030: hypothetical protein. (212 aa) |
| | EW14_1419 | Iron starvation-induced chlorophyll a(b) binding protein IsiA; Alternative locus ID: PMIT0604_1419; photosystem II CP43 protein (PsbC) homolog. (352 aa) |
| | rpmH | LSU ribosomal protein L34p; Alternative locus ID: PMIT0604_1432; Belongs to the bacterial ribosomal protein bL34 family. (45 aa) |
| | rpsN | SSU ribosomal protein S14p (S29e); Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site; Belongs to the universal ribosomal protein uS14 family. (100 aa) |
| | EW14_1455 | D-glycero-D-manno-heptose 1,7-bisphosphate phosphatasee; Alternative locus ID: PMIT0604_1455. (420 aa) |
| | EW14_1481 | Hypothetical protein; Alternative locus ID: PMIT0604_1481. (275 aa) |
| | EW14_1507 | Hypothetical protein; Alternative locus ID: PMIT0604_1507. (203 aa) |
| | EW14_1522 | Hypothetical protein; Alternative locus ID: PMIT0604_1522. (441 aa) |
| | EW14_1528 | Cytochrome C553 (soluble cytochrome f); Alternative locus ID: PMIT0604_1528. (109 aa) |
| | ftsH-4 | Cell division protein FtsH; 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) |
| | EW14_1572 | Riboflavin kinase; Alternative locus ID: PMIT0604_1572; FMN adenylyltransferase; Belongs to the ribF family. (307 aa) |
| | rpsP | SSU ribosomal protein S16p; Alternative locus ID: PMIT0604_1586; Belongs to the bacterial ribosomal protein bS16 family. (114 aa) |
| | pdhA | Pyruvate dehydrogenase E1 component alpha subunit; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (345 aa) |
| | EW14_1638 | Acyl-(acyl-carrier-protein)--UDP-N- acetylglucosamine O-acyltransferase; Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell. (280 aa) |
| | kaiC | Circadian clock protein KaiC; Core component of the KaiBC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. Binds to DNA. The KaiBC complex may act as a promoter-nonspecific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction; Belongs to the KaiC family. (509 aa) |
| | rplU | LSU ribosomal protein L21p; This protein binds to 23S rRNA in the presence of protein L20; Belongs to the bacterial ribosomal protein bL21 family. (146 aa) |
| | rpmA | LSU ribosomal protein L27p; Alternative locus ID: PMIT0604_1648; Belongs to the bacterial ribosomal protein bL27 family. (86 aa) |
| | EW14_1653 | Putative lumenal protein; Alternative locus ID: PMIT0604_1653; contains 8 pentapeptide repeats, sll0577 homolog. (200 aa) |
| | EW14_1659 | Hypothetical protein; Alternative locus ID: PMIT0604_1659; FIG001583: hypothetical protein; contains S4-like RNA binding domain. (263 aa) |
| | EW14_1661 | Pyridoxamine-phosphate oxidase; Alternative locus ID: PMIT0604_1661. (183 aa) |
| | EW14_1664 | Deoxyribodipyrimidine photolyase; Alternative locus ID: PMIT0604_1664. (384 aa) |
| | EW14_1747 | Hypothetical protein; Alternative locus ID: PMIT0604_1747; FIG01150344: hypothetical protein. (239 aa) |
| | EW14_1768 | Hypothetical protein; Alternative locus ID: PMIT0604_1768; Protein of unknown function DUF55. (152 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. (486 aa) |
| | atpC | ATP synthase epsilon chain; Produces ATP from ADP in the presence of a proton gradient across the membrane. (134 aa) |
| | EW14_1780 | Putative 30S ribosomal protein PSRP-3; Probably a ribosomal protein or a ribosome-associated protein; Belongs to the chloroplast-specific ribosomal protein cS23 family. (158 aa) |
| | EW14_1785 | Nicotinate-nucleotide adenylyltransferase bacterial NadD family; Alternative locus ID: PMIT0604_1785; Belongs to the NadD family. (192 aa) |
| | atpG | ATP synthase gamma chain; 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. (315 aa) |
| | atpA | ATP synthase alpha chain; Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit. (505 aa) |
| | atpH | ATP synthase delta chain; 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. (180 aa) |
| | atpF | ATP synthase B chain; Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0); Belongs to the ATPase B chain family. (170 aa) |
| | atpG-2 | ATP synthase B' chain; Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0). The b'-subunit is a diverged and duplicated form of b found in plants and photosynthetic bacteria. Belongs to the ATPase B chain family. (153 aa) |
| | atpE | ATP synthase C chain; 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 A chain; Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane. Belongs to the ATPase A chain family. (241 aa) |
| | ccsB | Cytochrome c-type bioproteinsis protein Ccs1/ResB; Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment. (428 aa) |
| | EW14_1813 | Hypothetical protein; Alternative locus ID: PMIT0604_1813; FIG00941839: hypothetical protein. (85 aa) |
| | rpsT | SSU ribosomal protein S20p; Binds directly to 16S ribosomal RNA. (106 aa) |
| | clpS | ATP-dependent Clp protease adaptor protein ClpS; Involved in the modulation of the specificity of the ClpAP- mediated ATP-dependent protein degradation; Belongs to the ClpS family. (105 aa) |
| | rpsJ | SSU ribosomal protein S10p (S20e); Involved in the binding of tRNA to the ribosomes. Belongs to the universal ribosomal protein uS10 family. (106 aa) |
| | rpsG | SSU ribosomal protein S7p (S5e); One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA; Belongs to the universal ribosomal protein uS7 family. (156 aa) |
| | rpsL | SSU ribosomal protein S12p (S23e); Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit. (124 aa) |
| | psaL | Photosystem I subunit XI (PsaL); Alternative locus ID: PMIT0604_1858. (199 aa) |
| | psaB | Photosystem I chlorophyll a apoprotein subunit Ib (PsaB); 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; Belongs to the PsaA/PsaB family. (706 aa) |
| | psaA | Photosystem I chlorophyll a apoprotein subunit Ia (PsaA); 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; Belongs to the PsaA/PsaB family. (767 aa) |
| | rpmE | LSU ribosomal protein L31p; Binds the 23S rRNA; Belongs to the bacterial ribosomal protein bL31 family. Type A subfamily. (86 aa) |
| | rpsI | SSU ribosomal protein S9p (S16e); Alternative locus ID: PMIT0604_1889; Belongs to the universal ribosomal protein uS9 family. (136 aa) |
| | rplM | LSU ribosomal protein L13p (L13Ae); This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly. (143 aa) |
| | rplQ | LSU ribosomal protein L17p; Alternative locus ID: PMIT0604_1892. (116 aa) |
| | rpsK | SSU ribosomal protein S11p (S14e); Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine- Dalgarno cleft in the 70S ribosome; Belongs to the universal ribosomal protein uS11 family. (130 aa) |
| | rpsM | SSU ribosomal protein S13p (S18e); Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits; these bridges are implicated in subunit movement. Contacts the tRNAs in the A and P-sites. Belongs to the universal ribosomal protein uS13 family. (121 aa) |
| | rpmJ | LSU ribosomal protein L36p; Alternative locus ID: PMIT0604_1896; Belongs to the bacterial ribosomal protein bL36 family. (38 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) |
| | rplO | LSU ribosomal protein L15p (L27Ae); Binds to the 23S rRNA; Belongs to the universal ribosomal protein uL15 family. (152 aa) |
| | rpsE | SSU ribosomal protein S5p (S2e); Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body. Belongs to the universal ribosomal protein uS5 family. (206 aa) |
| | rplR | LSU ribosomal protein L18p (L5e); This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. (122 aa) |
| | rplF | LSU ribosomal protein L6p (L9e); This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7/L12 stalk, and near the tRNA binding site of the peptidyltransferase center; Belongs to the universal ribosomal protein uL6 family. (179 aa) |
| | rpsH | SSU ribosomal protein S8p (S15Ae); One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit; Belongs to the universal ribosomal protein uS8 family. (133 aa) |
| | rplE | LSU ribosomal protein L5p (L11e); This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits; this bridge is implicated in subunit movement. Contacts the P site tRNA; the 5S rRNA and some of its associated proteins might help stabilize positioning of ribosome-bound tRNAs. (179 aa) |
| | rplX | LSU ribosomal protein L24p (L26e); One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit. (118 aa) |
| | rplN | LSU ribosomal protein L14p (L23e); Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome; Belongs to the universal ribosomal protein uL14 family. (121 aa) |
| | rpsQ | SSU ribosomal protein S17p (S11e); One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA. (88 aa) |
| | rpmC | LSU ribosomal protein L29p (L35e); Alternative locus ID: PMIT0604_1908; Belongs to the universal ribosomal protein uL29 family. (72 aa) |
| | rplP | LSU ribosomal protein L16p (L10e); Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs; Belongs to the universal ribosomal protein uL16 family. (144 aa) |
| | rpsC | SSU ribosomal protein S3p (S3e); Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation; Belongs to the universal ribosomal protein uS3 family. (243 aa) |
| | rplV | LSU ribosomal protein L22p (L17e); The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome. (128 aa) |
| | rpsS | SSU ribosomal protein S19p (S15e); Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA. (92 aa) |
| | rplB | LSU ribosomal protein L2p (L8e); One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity; this is somewhat controversial. Makes several contacts with the 16S rRNA in the 70S ribosome. Belongs to the universal ribosomal protein uL2 family. (287 aa) |
| | rplW | LSU ribosomal protein L23p (L23Ae); One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome; Belongs to the universal ribosomal protein uL23 family. (100 aa) |
| | rplD | LSU ribosomal protein L4p (L1e); Forms part of the polypeptide exit tunnel. (210 aa) |
| | rplC | LSU ribosomal protein L3p (L3e); One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit; Belongs to the universal ribosomal protein uL3 family. (206 aa) |
| | ndhN | Putative subunit of NAD(P)H:quinone oxidoreductase; 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. (158 aa) |
| | EW14_1936 | Photosystem I subunit II (PsaD); Alternative locus ID: PMIT0604_1936. (140 aa) |
| | EW14_1951 | Heme oxygenase; Alternative locus ID: PMIT0604_1952. (236 aa) |
| | EW14_1962 | Hypothetical protein; Alternative locus ID: PMIT0604_1963; FIG00940915: hypothetical protein. (61 aa) |
| | rimM | 16S rRNA processing protein RimM; An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes; Belongs to the RimM family. (179 aa) |
| | psaC | Photosystem I iron-sulfur center subunit VII (PsaC); 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 ch [...] (81 aa) |
| | gyrB | DNA gyrase subunit B; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. (655 aa) |
| | miaA | tRNA delta(2)-isopentenylpyrophosphate transferase; Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A); Belongs to the IPP transferase family. (299 aa) |
| | EW14_1995 | Serine acetyltransferase; Alternative locus ID: PMIT0604_1996. (244 aa) |
| | secA | Protein export cytoplasm protein SecA ATPase RNA helicase; 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. (943 aa) |
| | rpmI | LSU ribosomal protein L35p; Alternative locus ID: PMIT0604_2030; Belongs to the bacterial ribosomal protein bL35 family. (65 aa) |
| | rplT | LSU ribosomal protein L20p; Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit. (115 aa) |
| | rplI | LSU ribosomal protein L9p; Binds to the 23S rRNA. (151 aa) |
| | EW14_2042 | Replicative DNA helicase; Participates in initiation and elongation during chromosome replication; it exhibits DNA-dependent ATPase activity. Belongs to the helicase family. DnaB subfamily. (460 aa) |
| | rpsF | SSU ribosomal protein S6p; Binds together with S18 to 16S ribosomal RNA. (143 aa) |
