Rv1733c Family assigned · medium auto-curated

H37Rv Rv1733c · MTBC0 mtbc0_001845 · 210 aa · 1971927–1972559 (-) · RefSeq NP_216249.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)transmembrane protein
MTBC0 PGAP re-annotationhypothetical protein
Revised (this work)Contains Rv1733c (PF27099.1) domain(s); putative function inferred from the domain architecture.

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

Curated reference (UniProt)

UniProt P9WLS9 SwissProt · reviewed · Evidence at protein level
UniProt nameProbable membrane protein Rv1733c

Functional vocabulary (eggNOG-mapper, orthology transfer)

Orthologous group2E3P4

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 0.979 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 8 missense, 0 nonsense, 0 frameshift

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
Rv1733cPF27099.1 1.6e-1283–152 Rv1733c-like dormancy-induced membrane protein

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

Closest characterised functional partner: Rv3134c (universal stress protein), high confidence from genomic context alone (score 937 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv3134c universal stress protein 975 937 ctx cooccurence:647 coexpression:829 textmining:626
Rv2032 acg NAD(P)H nitroreductase 939 882 coexpression:860 textmining:510
Rv2627c hyp hypothetical protein 876 877 coexpression:860
Rv2626c hrp1 hypoxic response protein 950 861 coexpression:860 textmining:659
Rv2030c hyp hypothetical protein 881 860 coexpression:860
Rv1737c narK2 nitrate/nitrite transporter 872 860 coexpression:860
Rv1738 hyp hypothetical protein 922 845 coexpression:797 textmining:518
Rv2623 TB31.7 universal stress protein 878 843 coexpression:843
Rv1996 universal stress protein 870 843 coexpression:822
Rv2031c hspX alpha-crystallin 936 837 coexpression:804 textmining:625
Rv3127 hyp hypothetical protein 902 836 coexpression:813 textmining:432
Rv1736c narX nitrate reductase-like protein NarX 836 836 coexpression:836
Rv2028c universal stress protein 881 833 coexpression:740
Rv2625c rip3 zinc metalloprotease Rip3 832 833 coexpression:810
Rv3131 NAD(P)H nitroreductase 898 828 coexpression:806 textmining:433

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: transmembrane protein
  • MTBC0 PGAP product: hypothetical protein
  • Pfam (hmmscan --cut_ga): Rv1733c PF27099.1 (E=2e-12)
  • (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_216249.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Rv1733c (PF27099.1)
  • 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 2E3P4
  • Curated reference: UniProt P9WLS9 (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 — 92 functional partner(s); context anchor Rv3134c
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001845|Rv1733c|
MIATTRDREGATMITFRLRLPCRTILRVFSRNPLVRGTDRLEAVVMLLAVTVSLLTIPFAAAAGTAVHDSRSHVYAHQAQTRHPATATVIDHEGVIDSNTTATSAPPRTKITVPARWVVNGIERSGEVNAKPGTKSGDRVGIWVDSAGQLVDEPAPPARAIADAALAALGLWLSVAAVAGALLALTRAILIRVRNASWQHDIDSLFCTQR