Your Input: | |
| | metH | Unannotated protein; Catalyzes the transfer of a methyl group from methyl- cobalamin to homocysteine, yielding enzyme-bound cob(I)alamin and methionine. Subsequently, remethylates the cofactor using methyltetrahydrofolate. (1149 aa) |
| | CHR53_15885 | Unannotated protein; Belongs to the cytochrome P450 family. (409 aa) |
| | CHR53_15200 | Unannotated protein. (155 aa) |
| | CHR53_15140 | Unannotated protein. (256 aa) |
| | CHR53_15060 | Unannotated protein. (110 aa) |
| | CHR53_14880 | Unannotated protein. (150 aa) |
| | CHR53_14595 | Unannotated protein; Belongs to the cytochrome P450 family. (464 aa) |
| | CHR53_14465 | Unannotated protein. (378 aa) |
| | CHR53_14375 | Unannotated protein. (153 aa) |
| | CHR53_13865 | Unannotated protein. (256 aa) |
| | CHR53_13820 | Unannotated protein. (241 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. Belongs to the ThiC family. (590 aa) |
| | hydA | Unannotated protein. (472 aa) |
| | CHR53_13275 | Unannotated protein. (84 aa) |
| | CHR53_13000 | Unannotated protein. (227 aa) |
| | allB | Unannotated protein. (489 aa) |
| | CHR53_12915 | Unannotated protein. (786 aa) |
| | CHR53_11980 | Unannotated protein. (129 aa) |
| | CHR53_11745 | Unannotated protein. (171 aa) |
| | CHR53_11650 | Unannotated protein. (307 aa) |
| | hutI-2 | Unannotated protein. (424 aa) |
| | ppaC | Unannotated protein. (312 aa) |
| | ribBA | Unannotated protein; Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate; In the C-terminal section; belongs to the GTP cyclohydrolase II family. (397 aa) |
| | ribD | Unannotated protein; Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'- phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)-pyrimidinedione 5'- phosphate; In the C-terminal section; belongs to the HTP reductase family. (360 aa) |
| | CHR53_11110 | Unannotated protein. (781 aa) |
| | CHR53_11075 | Unannotated protein. (772 aa) |
| | corA | Unannotated protein; Mediates influx of magnesium ions. Belongs to the CorA metal ion transporter (MIT) (TC 1.A.35) family. (316 aa) |
| | CHR53_10840 | Unannotated protein. (82 aa) |
| | CHR53_10665 | Unannotated protein. (283 aa) |
| | hutI | Unannotated protein. (417 aa) |
| | CHR53_10100 | Unannotated protein. (277 aa) |
| | CHR53_10075 | Unannotated protein. (287 aa) |
| | rnz-2 | Unannotated protein; Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA. (278 aa) |
| | CHR53_10060 | Unannotated protein. (445 aa) |
| | CHR53_10025 | Unannotated protein; Belongs to the cytochrome P450 family. (395 aa) |
| | rnj-3 | Unannotated protein; An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and/or decay; Belongs to the metallo-beta-lactamase superfamily. RNA- metabolizing metallo-beta-lactamase-like family. Bacterial RNase J subfamily. (555 aa) |
| | rnhB | Unannotated protein; Endonuclease that specifically degrades the RNA of RNA-DNA hybrids. (261 aa) |
| | priA | Unannotated protein; 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. (803 aa) |
| | pyrC | Unannotated protein; Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate; Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily. (428 aa) |
| | CHR53_09335 | Unannotated protein. (98 aa) |
| | ileS | Unannotated protein; Catalyzes the attachment of isoleucine to tRNA(Ile). As IleRS can inadvertently accommodate and process structurally similar amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile). Belongs to the class-I aminoacyl-tRNA synthetase family. IleS type 1 subfamily. (923 aa) |
| | coxB | Unannotated protein; Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B). (384 aa) |
| | rnj-2 | Unannotated protein; An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and/or decay; Belongs to the metallo-beta-lactamase superfamily. RNA- metabolizing metallo-beta-lactamase-like family. Bacterial RNase J subfamily. (555 aa) |
| | CHR53_08705 | Unannotated protein. (351 aa) |
| | CHR53_08635 | Unannotated protein. (764 aa) |
| | CHR53_08590 | Unannotated protein. (567 aa) |
| | CHR53_08515 | Unannotated protein. (120 aa) |
| | prpE | Unannotated protein; Asymmetrically hydrolyzes Ap4p to yield AMP and ATP. (246 aa) |
| | CHR53_08300 | Unannotated protein. (798 aa) |
| | CHR53_08245 | Unannotated protein. (571 aa) |
| | CHR53_07695 | Unannotated protein. (74 aa) |
| | CHR53_07590 | Unannotated protein. (259 aa) |
| | CHR53_07575 | Unannotated protein. (327 aa) |
| | CHR53_07500 | Unannotated protein. (160 aa) |
| | CHR53_07495 | Unannotated protein. (279 aa) |
| | CHR53_06515 | Unannotated protein. (539 aa) |
| | CHR53_06430 | Unannotated protein. (153 aa) |
| | CHR53_06420 | Unannotated protein. (163 aa) |
| | CHR53_06410 | Unannotated protein; Belongs to the UPF0753 family. (872 aa) |
| | map-2 | Unannotated protein; Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed; Belongs to the peptidase M24A family. Methionine aminopeptidase type 1 subfamily. (249 aa) |
| | bioB | Unannotated protein; Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical-based mechanism; Belongs to the radical SAM superfamily. Biotin synthase family. (337 aa) |
| | CHR53_04940 | Unannotated protein. (235 aa) |
| | CHR53_04890 | Unannotated protein. (511 aa) |
| | CHR53_04645 | Unannotated protein. (312 aa) |
| | CHR53_04320 | Unannotated protein. (188 aa) |
| | CHR53_04085 | Unannotated protein. (158 aa) |
| | CHR53_04005 | Unannotated protein. (350 aa) |
| | CHR53_03965 | Unannotated protein. (834 aa) |
| | luxS | Unannotated protein; Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5-dihydroxy-2,3-pentadione (DPD). Belongs to the LuxS family. (153 aa) |
| | rnj | Unannotated protein; An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and/or decay; Belongs to the metallo-beta-lactamase superfamily. RNA- metabolizing metallo-beta-lactamase-like family. Bacterial RNase J subfamily. (557 aa) |
| | CHR53_03305 | Unannotated protein. (149 aa) |
| | CHR53_03265 | Unannotated protein. (799 aa) |
| | CHR53_03260 | Unannotated protein. (795 aa) |
| | CHR53_03220 | Unannotated protein. (568 aa) |
| | CHR53_03025 | Unannotated protein; Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N- terminal amino acids from various peptides. Belongs to the peptidase M17 family. (475 aa) |
| | CHR53_02860 | Unannotated protein. (1056 aa) |
| | CHR53_02760 | Unannotated protein. (759 aa) |
| | CHR53_02265 | Unannotated protein. (361 aa) |
| | CHR53_02140 | Unannotated protein. (351 aa) |
| | tsaD | Unannotated protein; Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction; Belongs to the KAE1 / TsaD family. (348 aa) |
| | CHR53_01640 | Unannotated protein; Belongs to the SprT family. (159 aa) |
| | CHR53_01395 | Unannotated protein. (394 aa) |
| | GCA_001636315_02798 | Unannotated protein. (139 aa) |
| | CHR53_00980 | Unannotated protein; Belongs to the peptidase M24B family. (372 aa) |
| | adk | Unannotated protein; Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism; Belongs to the adenylate kinase family. (216 aa) |
| | rpsZ | Unannotated protein; 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. (61 aa) |
| | rpoC | Unannotated protein; DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. (1199 aa) |
| | cysS | Unannotated protein; Belongs to the class-I aminoacyl-tRNA synthetase family. (465 aa) |
| | gltX | Unannotated protein; Catalyzes the attachment of glutamate to tRNA(Glu) in a two- step reaction: glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu). (485 aa) |
| | CHR53_00530 | Unannotated protein. (182 aa) |
| | ftsH | Unannotated 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. (652 aa) |
| | tadA | Unannotated protein; Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2); Belongs to the cytidine and deoxycytidylate deaminase family. (171 aa) |
| | CHR53_28080 | Unannotated protein; Belongs to the prokaryotic molybdopterin-containing oxidoreductase family. (668 aa) |
| | CHR53_27940 | Unannotated protein. (190 aa) |
| | CHR53_27855 | Unannotated protein. (134 aa) |
| | pepT | Unannotated protein; Cleaves the N-terminal amino acid of tripeptides. Belongs to the peptidase M20B family. (410 aa) |
| | CHR53_27435 | Unannotated protein. (622 aa) |
| | CHR53_27415 | Unannotated protein. (115 aa) |
| | fdnG | Unannotated protein; Belongs to the prokaryotic molybdopterin-containing oxidoreductase family. (789 aa) |
| | CHR53_27370 | Unannotated protein; Necessary for formate dehydrogenase activity. Belongs to the FdhE family. (271 aa) |
| | fba | Unannotated protein. (285 aa) |
| | tdk | Unannotated protein. (202 aa) |
| | nuoB | Unannotated protein; NDH-1 shuttles electrons from NADH, 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 a menaquinone. 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. (170 aa) |
| | nuoI | Unannotated protein; NDH-1 shuttles electrons from NADH, 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 ubiquinone. 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. (141 aa) |
| | CHR53_26910 | Unannotated protein. (304 aa) |
| | CHR53_26800 | Unannotated protein; Belongs to the Dps family. (151 aa) |
| | CHR53_26675 | Unannotated protein. (543 aa) |
| | CHR53_26500 | Unannotated protein. (254 aa) |
| | GCA_001636315_02146 | Unannotated protein. (803 aa) |
| | GCA_001636315_02135 | Unannotated protein. (538 aa) |
| | CHR53_26100 | Unannotated protein. (520 aa) |
| | CHR53_26075 | Unannotated protein; Belongs to the peptidase M17 family. (463 aa) |
| | cutC-2 | Unannotated protein; Participates in the control of copper homeostasis. Belongs to the CutC family. (227 aa) |
| | CHR53_26010 | Unannotated protein. (584 aa) |
| | CHR53_25805 | Unannotated protein. (359 aa) |
| | deoB-2 | Unannotated protein; Phosphotransfer between the C1 and C5 carbon atoms of pentose; Belongs to the phosphopentomutase family. (392 aa) |
| | CHR53_25550 | Unannotated protein. (458 aa) |
| | manA | Unannotated protein; Belongs to the mannose-6-phosphate isomerase type 1 family. (319 aa) |
| | CHR53_25370 | Unannotated protein; Destroys radicals which are normally produced within the cells and which are toxic to biological systems. Belongs to the Cu-Zn superoxide dismutase family. (210 aa) |
| | CHR53_25250 | Unannotated protein. (263 aa) |
| | CHR53_25220 | Unannotated protein. (316 aa) |
| | kynB | Unannotated protein; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. (207 aa) |
| | CHR53_25105 | Unannotated protein; This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis; Belongs to the cytidine and deoxycytidylate deaminase family. (132 aa) |
| | ureA-2 | Unannotated protein; Belongs to the urease gamma subunit family. (100 aa) |
| | ureC-2 | Unannotated protein. (570 aa) |
| | ureE-2 | Unannotated protein; Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly. Belongs to the UreE family. (151 aa) |
| | ureF-2 | Unannotated protein; Required for maturation of urease via the functional incorporation of the urease nickel metallocenter. (228 aa) |
| | ureG-2 | Unannotated protein; Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG. (203 aa) |
| | ureD-2 | Unannotated protein; Required for maturation of urease via the functional incorporation of the urease nickel metallocenter. (274 aa) |
| | fdhA | Unannotated protein. (405 aa) |
| | CHR53_24010 | Unannotated protein. (281 aa) |
| | cutC | Unannotated protein; Participates in the control of copper homeostasis. Belongs to the CutC family. (216 aa) |
| | CHR53_23665 | Unannotated protein. (351 aa) |
| | CHR53_23520 | Unannotated protein. (351 aa) |
| | CHR53_23400 | Unannotated protein. (111 aa) |
| | uvrA | Unannotated protein; The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate. (957 aa) |
| | hisD | Unannotated protein; Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine. (423 aa) |
| | gpmI | Unannotated protein; Catalyzes the interconversion of 2-phosphoglycerate and 3- phosphoglycerate; Belongs to the BPG-independent phosphoglycerate mutase family. (510 aa) |
| | metE | Unannotated protein; Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation; Belongs to the vitamin-B12 independent methionine synthase family. (757 aa) |
| | CHR53_22730 | Unannotated protein. (147 aa) |
| | CHR53_22635 | Unannotated protein. (78 aa) |
| | pepA | Unannotated protein; Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N- terminal amino acids from various peptides. (502 aa) |
| | CHR53_22550 | Unannotated protein; Destroys radicals which are normally produced within the cells and which are toxic to biological systems. Belongs to the Cu-Zn superoxide dismutase family. (182 aa) |
| | CHR53_22450 | Unannotated protein. (251 aa) |
| | fucI | Unannotated protein; Converts the aldose L-fucose into the corresponding ketose L- fuculose. (596 aa) |
| | CHR53_22175 | Unannotated protein; Belongs to the Dps family. (148 aa) |
| | GCA_001636315_01304 | Unannotated protein. (378 aa) |
| | CHR53_22025 | Unannotated protein. (389 aa) |
| | GCA_001636315_01285 | Unannotated protein. (549 aa) |
| | GCA_001636315_01278 | Unannotated protein. (359 aa) |
| | CHR53_21965 | Unannotated protein. (368 aa) |
| | menD | Unannotated protein; Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2- succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC). Belongs to the TPP enzyme family. MenD subfamily. (583 aa) |
| | CHR53_21760 | Unannotated protein. (190 aa) |
| | CHR53_21655 | Unannotated protein; Belongs to the cytochrome c-552 family. (483 aa) |
| | CHR53_21565 | Unannotated protein. (473 aa) |
| | CHR53_21315 | Unannotated protein. (365 aa) |
| | accD | Unannotated protein; Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl-CoA; Belongs to the AccD/PCCB family. (292 aa) |
| | mutM | Unannotated protein; Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic/apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates. (277 aa) |
| | nrdR | Unannotated protein; Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes; Belongs to the NrdR family. (153 aa) |
| | clpX | Unannotated protein; ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP. (419 aa) |
| | alaS | Unannotated protein; Catalyzes the attachment of alanine to tRNA(Ala) in a two- step reaction: alanine is first activated by ATP to form Ala-AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain. (879 aa) |
| | CHR53_20185 | Unannotated protein. (153 aa) |
| | dnaJ | Unannotated protein; Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins and by disaggregating proteins, also in an autonomous, DnaK-independent fashion. Unfolded proteins bind initially to DnaJ; upon interaction with the DnaJ-bound protein, DnaK hydrolyzes its bound ATP, resulting in the formation of a stable complex. GrpE releases ADP from DnaK; ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK [...] (378 aa) |
| | ybeY | Unannotated protein; Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA. (156 aa) |
| | CHR53_20040 | Unannotated protein; This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis; Belongs to the cytidine and deoxycytidylate deaminase family. (133 aa) |
| | dnaG | Unannotated protein; RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication. (602 aa) |
| | CHR53_19990 | Unannotated protein. (122 aa) |
| | nfo | Unannotated protein; Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin. (297 aa) |
| | ispG | Unannotated protein; Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME- 2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate. Belongs to the IspG family. (369 aa) |
| | CHR53_19675 | Unannotated protein. (68 aa) |
| | CHR53_19670 | Unannotated protein. (804 aa) |
| | CHR53_19645 | Unannotated protein. (353 aa) |
| | rnz | Unannotated protein; Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA; Belongs to the RNase Z family. (307 aa) |
| | deoB | Unannotated protein; Phosphotransfer between the C1 and C5 carbon atoms of pentose; Belongs to the phosphopentomutase family. (394 aa) |
| | CHR53_19050 | Unannotated protein. (82 aa) |
| | folE | Unannotated protein. (188 aa) |
| | CHR53_18780 | Unannotated protein; Component of the menaquinol-cytochrome c reductase complex. (256 aa) |
| | CHR53_18535 | Unannotated protein. (158 aa) |
| | mntR | Unannotated protein; Central regulator of manganese homeostasis. Belongs to the DtxR/MntR family. (140 aa) |
| | CHR53_17775 | Unannotated protein. (178 aa) |
| | ureA | Unannotated protein; Belongs to the urease gamma subunit family. (100 aa) |
| | ureC | Unannotated protein. (570 aa) |
| | ureE | Unannotated protein; Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly. Belongs to the UreE family. (151 aa) |
| | ureF | Unannotated protein; Required for maturation of urease via the functional incorporation of the urease nickel metallocenter. (232 aa) |
| | ureG | Unannotated protein; Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG. (203 aa) |
| | ureD | Unannotated protein; Required for maturation of urease via the functional incorporation of the urease nickel metallocenter. (274 aa) |
| | CHR53_17375 | Unannotated protein; Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic/apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates. (269 aa) |
| | CHR53_17240 | Unannotated protein. (324 aa) |
| | CHR53_17220 | Unannotated protein. (779 aa) |
| | qoxA | Unannotated protein; Catalyzes quinol oxidation with the concomitant reduction of oxygen to water. Subunit II transfers the electrons from a quinol to the binuclear center of the catalytic subunit I. (301 aa) |
| | map | Unannotated protein; Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed; Belongs to the peptidase M24A family. Methionine aminopeptidase type 1 subfamily. (246 aa) |
| | queC | Unannotated protein; Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)). (219 aa) |
| | CHR53_16230 | Unannotated protein. (214 aa) |
| | CHR53_16120 | Unannotated protein. (344 aa) |
| | CHR53_16095 | Unannotated protein. (143 aa) |
| | CHR53_16080 | Unannotated protein. (251 aa) |
| | GCA_001636315_00035 | Unannotated protein. (446 aa) |
| | GCA_001636315_00029 | Unannotated protein. (760 aa) |
