Rv2146c Family assigned · medium auto-curated

H37Rv Rv2146c · MTBC0 mtbc0_002282 · 96 aa · 2433045–2433335 (-) · RefSeq NP_216662.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)transmembrane protein
MTBC0 PGAP re-annotationYggT family protein
Revised (this work)YggT family protein. Pfam: CCB3_YggT (PF02325.24).

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

Curated reference (UniProt)

UniProt O06230 TrEMBL · unreviewed · Predicted
UniProt namePossible conserved transmembrane protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
eggNOG descriptionintegral membrane protein
Orthologous groupCOG0762
KEGG orthology K02221

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 n/a
Polymorphic sites (≥ 0.1% of strains) 0 synonymous, 2 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
CCB3_YggTPF02325.24 1.2e-121–92 CCB3/YggT

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

Closest characterised functional partner: sepF (cell division protein SepF), high confidence from genomic context alone (score 946 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2147c sepF cell division protein SepF 953 946 ctx neighborhood:747 coexpression:795
Rv2145c wag31 cell wall synthesis protein Wag31 899 892 ctx neighborhood:722 coexpression:434
Rv2150c ftsZ cell division protein FtsZ 850 844 ctx neighborhood:569 coexpression:652
Rv2148c hyp hypothetical protein 812 782 ctx neighborhood:571 coexpression:513
Rv2256c hyp hypothetical protein 773 774 ctx cooccurence:763
Rv2413c hyp hypothetical protein 742 726 ctx cooccurence:719
Rv2144c transmembrane protein 682 682 ctx neighborhood:672
Rv2050 rbpA RNA polymerase-binding protein RbpA 663 663 ctx cooccurence:658
Rv3009c gatB aspartyl/glutamyl-tRNA(Asn/Gln) amidotransferase subunit B 660 660 coexpression:649
Rv2680 hyp hypothetical protein 641 641 ctx cooccurence:637
Rv1002c pmt dolichyl-phosphate-mannose--protein mannosyltransferase 638 638 ctx cooccurence:637
Rv0807 hyp hypothetical protein 630 630 ctx cooccurence:629
Rv2169c transmembrane protein 627 627 ctx cooccurence:612
Rv2699c hyp hypothetical protein 621 621 ctx cooccurence:618
Rv2745c clgR transcriptional regulator ClgR 599 599 ctx cooccurence:595

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: YggT family protein
  • Pfam (hmmscan --cut_ga): CCB3_YggT PF02325.24 (E=1e-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_216662.1)
  • Domains: Pfam-A via hmmscan --cut_ga — CCB3_YggT (PF02325.24)
  • 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 COG0762
  • Curated reference: UniProt O06230 (TrEMBL, unreviewed; Predicted)
  • 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 — 73 functional partner(s); context anchor sepF
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002282|Rv2146c|
MVVFFQILGFALFIFWLLLIARVVVEFIRSFSRDWRPTGVTVVILEIIMSITDPPVKVLRRLIPQLTIGAVRFDLSIMVLLLVAFIGMQLAFGAAA