Rv1279 Family assigned · medium auto-curated

H37Rv Rv1279 · MTBC0 mtbc0_001369 · 528 aa · 1439045–1440631 (+) · RefSeq NP_215795.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)GMC-type oxidoreductase
MTBC0 PGAP re-annotationGMC family oxidoreductase N-terminal domain-containing protein
Revised (this work)GMC family oxidoreductase N-terminal domain-containing protein. Pfam: GMC_oxred_N (PF00732.26), GMC_oxred_C (PF05199.20).

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

Curated reference (UniProt)

UniProt P9WMV5 SwissProt · reviewed · Evidence at protein level
UniProt nameUncharacterized GMC-type oxidoreductase Rv1279
EC (curated) EC 1.1.-.-

UniProt still lists this protein as Uncharacterized GMC-type oxidoreductase Rv1279; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category E Amino acid transport and metabolism
eggNOG descriptionBelongs to the GMC oxidoreductase family
Orthologous groupCOG2303
EC number EC 1.1.99.1
KEGG orthology K00108
KEGG pathways map00260, map01100
KEGG modules M00555
Gene Ontology (13) GO:0005575, GO:0005618, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0005886, GO:0016020, GO:0030312, GO:0044424, GO:0044444, GO:0044464 +1 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) pseudogene candidate

pN/pS 0.801 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 6 missense, 1 nonsense, 1 frameshift
Disruption 2 distinct premature-stop/frameshift site(s); most common in 1.62% of strains (2353) · 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
GMC_oxred_NPF00732.26 1.5e-606–298 GMC oxidoreductase
GMC_oxred_CPF05199.20 1.9e-36383–519 GMC oxidoreductase

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv1278 hyp hypothetical protein 968 969 ctx neighborhood:853 coexpression:796
Rv1277 hyp hypothetical protein 889 889 ctx neighborhood:853
Rv2350c plcB membrane-associated phospholipase B 805 805 database:800
Rv2349c plcC phospholipase C 803 803 database:800
Rv2351c plcA membrane-associated phospholipase A 802 803 database:800
Rv0437c psd phosphatidylserine decarboxylase 808 801 database:800
Rv1755c plcD Rv1755c, (MT1799, MTCY28.21c), len: 280 aa. Probable plcD, phospholipase C 4 (fragment) (see citations below),highly similar to C-terminus o 800 801 database:800
Rv2194 qcrC ubiquinol-cytochrome C reductase cytochrome subunit C 785 775 experimental:762
Rv2267c stf3 hyp hypothetical protein 756 746 experimental:411 database:583
Rv1691 hyp hypothetical protein 756 746 experimental:411 database:583
Rv3529c hyp hypothetical protein 754 744 experimental:411 database:583
Rv0832 PE_PGRS12 PE-PGRS family protein PE_PGRS12 739 729 database:573
Rv2328 PE23 PE family protein PE23 739 729 database:573
Rv3812 PE_PGRS62 PE-PGRS family protein PE_PGRS62 739 729 database:573
Rv3036c TB22.2 hyp hypothetical protein 739 729 database:573

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: GMC-type oxidoreductase
  • MTBC0 PGAP product: GMC family oxidoreductase N-terminal domain-containing protein
  • Pfam (hmmscan --cut_ga): GMC_oxred_N PF00732.26 (E=2e-60), GMC_oxred_C PF05199.20 (E=2e-36)
  • (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_215795.1)
  • Domains: Pfam-A via hmmscan --cut_ga — GMC_oxred_N (PF00732.26), GMC_oxred_C (PF05199.20)
  • 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 COG2303
  • Curated reference: UniProt P9WMV5 (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 — 33 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001369|Rv1279|
MDTQSDYVVVGTGSAGAVVASRLSTDPATTVVALEAGPRDKNRFIGVPAAFSKLFRSEIDWDYLTEPQPELDGREIYWPRGKVLGGSSSMNAMMWVRGFASDYDEWAARAGPRWSYADVLGYFRRIENVTAAWHFVSGDDSGVTGPLHISRQRSPRSVTAAWLAAARECGFAAARPNSPRPEGFCETVVTQRRGARFSTADAYLKPAMRRKNLRVLTGATATRVVIDGDRAVGVEYQSDGQTRIVYARREVVLCAGAVNSPQLLMLSGIGDRDHLAEHDIDTVYHAPEVGCNLLDHLVTVLGFDVEKDSLFAAEKPGQLISYLLRRRGMLTSNVGEAYGFVRSRPELKLPDLELIFAPAPFYDEALVPPAGHGVVFGPILVAPQSRGQITLRSADPHAKPVIEPRYLSDLGGVDRAAMMAGLRICARIAQARPLRDLLGSIARPRNSTELDEATLELALATCSHTLYHPMGTCRMGSDEASVVDPQLRVRGVDGLRVADASVMPSTVRGHTHAPSVLIGEKAADLIRS