ctpG Resolved · high auto-curated

H37Rv Rv1992c · MTBC0 mtbc0_002119 · 771 aa · 2258604–2260919 (-) · RefSeq NP_216508.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)cation transporter ATPase G
MTBC0 PGAP re-annotationcation transporter ATPase CptG
Revised (this work)Cation transporter ATPase CptG. Pfam: E1-E2_ATPase (PF00122.26), Hydrolase (PF00702.33).

Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.

Curated reference (UniProt)

UniProt P9WPS7 SwissProt · reviewed · Evidence at protein level
UniProt nameProbable cation-transporting ATPase G
EC (curated) EC 7.2.2.-

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category P Inorganic ion transport and metabolism
Preferred namecadA
eggNOG descriptionATPase, P-type (transporting), HAD superfamily, subfamily IC
Orthologous groupCOG2217
EC number EC 3.6.3.3, EC 3.6.3.4, EC 3.6.3.5, EC 3.6.3.54
KEGG orthology K01533, K01534, K12950, K12951, K12954, K12956, K17686, K21887
KEGG pathways map01524, map04016
Gene Ontology (18) GO:0005575, GO:0005623, GO:0005886, GO:0005887, GO:0008150, GO:0010035, GO:0010038, GO:0016020, GO:0016021, GO:0031224, GO:0031226, GO:0042221 +6 more

Orthology-based transfer (eggNOG 5.0.2, diamond). EC/KO/GO/CAZy are computed annotations, not manual curation; cross-check against the primary literature before treating a specific reaction as established.

Conservation & selection (intra-MTBC, 145 209 strains)

pN/pS 0.526 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 11 synonymous, 15 missense, 0 nonsense, 1 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.14% of strains (207) · clonal

pN/pS from segregating SNPs (singletons removed) normalised by possible sites. Low pN/pS = purifying selection (a strong signal that a "hypothetical" is a real, constrained gene). A high pN/pS is ambiguous: relaxed constraint or positive selection (drug resistance, antigenic variation) inflate it; e.g. rpoB/katG/pncA score high here for resistance, not loss of function. A clonal disruption (one allele over a clade) suggests lineage pseudogenisation; a convergent one (many independent alleles) is typical of resistance loss-of-function.

Domains (Pfam, hmmscan --cut_ga)

PfamAccessioni-EvalueResiduesDescription
E1-E2_ATPasePF00122.26 2.9e-24262–361 P-type ATPase actuator domain
HydrolasePF00702.33 2.3e-32456–663 haloacid dehalogenase-like hydrolase

Functional interaction network (STRING v12, guilt-by-association)

Closest characterised functional partner: cmtR (HTH-type transcriptional regulator CmtR), high confidence from genomic context alone (score 780 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1993c hyp hypothetical protein 992 963 ctx neighborhood:801 coexpression:820 textmining:802
Rv1994c cmtR HTH-type transcriptional regulator CmtR 892 780 ctx neighborhood:663 textmining:533
Rv1991A mazE6 antitoxin MazE6 579 560 ctx neighborhood:536
Rv1991c mazF6 mRNA interferase MazF6 551 551 ctx neighborhood:536
Rv0432 sodC superoxide dismutase 560 523 database:462
Rv0846c mmcO oxidase 604 517
Rv1995 hyp hypothetical protein 636 445 ctx neighborhood:440
Rv1997 ctpF cation transporter ATPase F 517 405
Rv1990A Rv1990A, len: 111 aa. Possible dehydrogenase (fragment), similar to N-terminal part of several dehydrogenases and hypothetical proteins, e.g 405 402
Rv0967 csoR copper-sensing transcriptional repressor CsoR 406 296
Rv0103c ctpB cation-transporter P-type ATPase B 433 272
Rv0092 ctpA cation transporter ATPase A 456 271
Rv0107c ctpI cation-transporter ATPase I 471 262
Rv0362 mgtE Mg2+ transport transmembrane protein MgtE 452 187
Rv0908 ctpE metal cation transporter ATPase E 413 184

STRING combines evidence channels (neighborhood, fusion, cooccurrence, coexpression, experimental, database, text-mining) into a 0–1000 score. The ctx badge marks edges carried by the genomic-context channels (conserved neighborhood, fusion, phylogenetic co-occurrence), which are independent of orthology and structure and the strongest signal for an unknown gene. The no text-mining column recomputes the score from data alone, so a link that does not depend on the literature is visible. Association is a function hypothesis, not proof: corroborate with the operon context and the primary literature before assigning a function.

Evidence

  • Legacy H37Rv annotation: cation transporter ATPase G
  • MTBC0 PGAP product: cation transporter ATPase CptG
  • Pfam (hmmscan --cut_ga): E1-E2_ATPase PF00122.26 (E=3e-24), Hydrolase PF00702.33 (E=2e-32)
  • (auto-curated by rules from PGAP + Pfam + Foldseek; not hand-reviewed)

Sources

  • Ancestral sequence & coordinates: Harrison LB et al. (2024), An imputed ancestral reference genome for the MTBC, doi:10.1101/2023.09.07.556366
  • Product annotation: NCBI PGAP on MTBC0; legacy from H37Rv NC_000962.3 (RefSeq NP_216508.1)
  • Domains: Pfam-A via hmmscan --cut_ga — E1-E2_ATPase (PF00122.26), Hydrolase (PF00702.33)
  • Sequence-level signal: ESM Atlas (EvolutionaryScale × BioHub) — exploratory
  • Controlled vocabulary: eggNOG-mapper 2.1.12 (Cantalapiedra et al. 2021, doi:10.1093/molbev/msab293), eggNOG 5.0 DB (Huerta-Cepas et al. 2019) — OG COG2217
  • Curated reference: UniProt P9WPS7 (SwissProt, reviewed; Evidence at protein level)
  • Intra-MTBC selection: pN/pS and disruption from SPDI variants of 145 209 MTBC strains (this work, local collection vs H37Rv NC_000962.3)
  • Interaction network: STRING v12.0 (Szklarczyk et al. 2023, doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 — 16 functional partner(s); context anchor cmtR
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002119|Rv1992c|ctpG
MTTVVDAEVQLTVVSDAAGRMRVQATGFQFDAGRAVAIEDTVGKVAGVQAVHAYPRTASIVIWYSRAICDTAAILSAIIDAETVPAAAVPAYASRSASNRKAGVVQKIIDWSTRTLSGVRRDVAAQPSGETSDACCDGEDNEDREPEQLWQVAKLRRAAFSGVLLTASLVAAWAYPLWPVVLGLKALALAVGASTFVPSSLKRLAEGRVGVGTLMTIAALGAVALGELGEAATLAFLFSISEGLEEYATARTRRGLRALLSLVPDQATVLREGTETIVASTELHVGDQMIVKPGERLATDGIIRAGRTALDVSAITGESVPVEVGPGDEVFAGSINGLGVLQVGVTATAANNSLARIVHIVEAEQVRKGASQRLADCIARPLVPSIMIAAALIAGTGSVLGNPLVWIERALVVLVAAAPCALAIAVPVTVVASIGAASRLGVLIKGGAALETLGTIRAVALDKTGTLTANRPVVIDVATTNGATREEVLAVAAALEARSEHPLAVAVLAATQATTAASDVQAVPGAGLIGRLDGRVVRLGRPGWLDAAELADHVACMQQAGATAVLVERDQQLLGAIAVRDELRPEAAEVVAGLRTGGYQVTMLTGDNHATAAALAAQAGIEQVHAELRPEDKAHLVAQLRARQPTAMVGDGVNDAPALAAADLGIAMGAMGTDVAIETADVALMGQDLRHLPQALDHARRSRQIMVQNVGLSLSIITVLMPLALFGILGLAAVVLVHEFTEVIVIANGVRAGRIKPLAGPPKTPDRTIPG