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| mobB | Unannotated protein. (176 aa) | ||||
| mobA | Unannotated protein; Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo-MPT) cofactor (Moco or molybdenum cofactor) to form Mo-molybdopterin guanine dinucleotide (Mo-MGD) cofactor; Belongs to the MobA family. (191 aa) | ||||
| GCA_000406125_00043 | Unannotated protein; Belongs to the short-chain dehydrogenases/reductases (SDR) family. (265 aa) | ||||
| GCA_000406125_00044 | Unannotated protein. (214 aa) | ||||
| thiH | Unannotated protein. (382 aa) | ||||
| thiG | Unannotated protein; Catalyzes the rearrangement of 1-deoxy-D-xylulose 5-phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S. (259 aa) | ||||
| thiS | Unannotated protein. (66 aa) | ||||
| GCA_000406125_00208 | Unannotated protein. (249 aa) | ||||
| thiE | Unannotated protein; Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP). Belongs to the thiamine-phosphate synthase family. (211 aa) | ||||
| thiC | Unannotated protein; Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction. (653 aa) | ||||
| GCA_000406125_00953 | Unannotated protein. (81 aa) | ||||
| GCA_000406125_00954 | Unannotated protein. (138 aa) | ||||
| GCA_000406125_00955 | Unannotated protein. (318 aa) | ||||
| GCA_000406125_00956 | Unannotated protein. (362 aa) | ||||
| csdE | Unannotated protein. (147 aa) | ||||
| csdA | Unannotated protein. (401 aa) | ||||
| thiI | Unannotated protein; Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS. (482 aa) | ||||
| modF | Unannotated protein. (489 aa) | ||||
| modE | Unannotated protein. (263 aa) | ||||
| acrZ | Unannotated protein; AcrA-AcrB-AcrZ-TolC is a drug efflux protein complex with a broad substrate specificity. This protein binds to AcrB and is required for efflux of some but not all substrates, suggesting it may influence the specificity of drug export. (49 aa) | ||||
| modA | Unannotated protein. (261 aa) | ||||
| modB | Unannotated protein; Part of the binding-protein-dependent transport system for molybdenum; probably responsible for the translocation of the substrate across the membrane; Belongs to the binding-protein-dependent transport system permease family. CysTW subfamily. (229 aa) | ||||
| modC | Unannotated protein; Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system; Belongs to the ABC transporter superfamily. Molybdate importer (TC 3.A.1.8) family. (352 aa) | ||||
| moeB | Unannotated protein. (252 aa) | ||||
| moeA | Unannotated protein; Catalyzes the insertion of molybdate into adenylated molybdopterin with the concomitant release of AMP. Belongs to the MoeA family. (411 aa) | ||||
| moaA | Unannotated protein; Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate. (340 aa) | ||||
| moaB | Unannotated protein; May be involved in the biosynthesis of molybdopterin. Belongs to the MoaB/Mog family. (170 aa) | ||||
| moaC | Unannotated protein; Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP); Belongs to the MoaC family. (160 aa) | ||||
| moaD | Unannotated protein. (81 aa) | ||||
| moaE | Unannotated protein. (150 aa) | ||||
| sufE | Unannotated protein. (138 aa) | ||||
| sufS | Unannotated protein; Cysteine desulfurases mobilize the sulfur from L-cysteine to yield L-alanine, an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Component of the suf operon, which is activated and required under specific conditions such as oxidative stress and iron limitation. Acts as a potent selenocysteine lyase in vitro, that mobilizes selenium from L- selenocysteine. Selenocysteine lyase activity is however unsure in vivo. (407 aa) | ||||
| GCA_000406125_02268 | Unannotated protein. (732 aa) | ||||
| thiD | Unannotated protein. (267 aa) | ||||
| iscX | Unannotated protein. (66 aa) | ||||
| fdx | Unannotated protein. (111 aa) | ||||
| hscA | Unannotated protein; Chaperone involved in the maturation of iron-sulfur cluster- containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB. Involved in the maturation of IscU. (616 aa) | ||||
| hscB | Unannotated protein; Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA; Belongs to the HscB family. (179 aa) | ||||
| iscA | Unannotated protein; Is able to transfer iron-sulfur clusters to apo-ferredoxin. Multiple cycles of [2Fe2S] cluster formation and transfer are observed, suggesting that IscA acts catalytically. Recruits intracellular free iron so as to provide iron for the assembly of transient iron-sulfur cluster in IscU in the presence of IscS, L-cysteine and the thioredoxin reductase system TrxA/TrxB. (107 aa) | ||||
| iscU | Unannotated protein; A scaffold on which IscS assembles Fe-S clusters. It is likely that Fe-S cluster coordination is flexible as the role of this complex is to build and then hand off Fe-S clusters. (128 aa) | ||||
| iscS | Unannotated protein; Master enzyme that delivers sulfur to a number of partners involved in Fe-S cluster assembly, tRNA modification or cofactor biosynthesis. Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine. Functions as a sulfur delivery protein for Fe-S cluster synthesis onto IscU, an Fe-S scaffold assembly protein, as well as other S acceptor proteins. (404 aa) | ||||
| iscR | Unannotated protein; Regulates the transcription of several operons and genes involved in the biogenesis of Fe-S clusters and Fe-S-containing proteins. (164 aa) | ||||
| erpA | Unannotated protein; Required for insertion of 4Fe-4S clusters for at least IspG. (114 aa) | ||||
| clcA | Unannotated protein. (465 aa) | ||||
| GCA_000406125_03086 | Unannotated protein. (255 aa) | ||||
| nsrR | Unannotated protein; Nitric oxide-sensitive repressor of genes involved in protecting the cell against nitrosative stress. May require iron for activity. (141 aa) | ||||
| djlA | Unannotated protein; Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB/RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host. (319 aa) | ||||
| GCA_000406125_03408 | Unannotated protein. (149 aa) | ||||
| GCA_000406125_03409 | Unannotated protein. (49 aa) | ||||
| GCA_000406125_03613 | Unannotated protein. (349 aa) | ||||
| nfuA | Unannotated protein; Involved in iron-sulfur cluster biogenesis. Binds a 4Fe-4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe/S proteins. Could also act as a scaffold/chaperone for damaged Fe/S proteins. (191 aa) | ||||
| cyaY | Unannotated protein; Involved in iron-sulfur (Fe-S) cluster assembly. May act as a regulator of Fe-S biogenesis. (106 aa) | ||||