Rv1906c Family assigned · medium auto-curated

H37Rv Rv1906c · MTBC0 mtbc0_002021 · 156 aa · 2170535–2171005 (-) · RefSeq NP_216422.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationhypothetical protein
Revised (this work)Contains Rv1352 (PF27111.1) 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 O07726 TrEMBL · unreviewed · Evidence at protein level
UniProt nameConserved protein

UniProt still lists this protein as Conserved protein; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category P Inorganic ion transport and metabolism
eggNOG descriptionABC-type Fe3 transport system, periplasmic component
Orthologous groupCOG1840

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 0.347 · purifying
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 1 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
Rv1352PF27111.1 2.7e-2743–114 Rv1352-like extracellular domain

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

Closest characterised functional partner: aao (D-amino acid oxidase), high confidence from genomic context alone (score 722 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv1905c aao D-amino acid oxidase 942 722 ctx neighborhood:717 textmining:803
Rv0941c hyp hypothetical protein 716 716 ctx cooccurence:715
Rv2721c hyp hypothetical protein 674 674 ctx cooccurence:666
Rv0538 membrane protein 665 653 ctx cooccurence:618
Rv1904 hyp hypothetical protein 869 639 ctx cooccurence:482 textmining:652
Rv3810 pirG cell surface protein 620 621 ctx cooccurence:617
Rv2015c hyp hypothetical protein 603 603 ctx cooccurence:600
Rv0479c membrane protein 594 595 ctx cooccurence:590
Rv2743c hyp hypothetical protein 583 584 ctx cooccurence:581
Rv1765c hyp hypothetical protein 575 576 ctx cooccurence:572
Rv1836c hyp hypothetical protein 572 572 ctx cooccurence:549
Rv2719c chiZ membrane protein 564 564 ctx cooccurence:545
Rv1648 transmembrane protein 546 546 ctx cooccurence:546
Rv1111c hyp hypothetical protein 523 523 ctx cooccurence:520
Rv1364c sigma factor regulatory protein 524 519 coexpression:505

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: hypothetical protein
  • MTBC0 PGAP product: hypothetical protein
  • Pfam (hmmscan --cut_ga): Rv1352 PF27111.1 (E=3e-27)
  • (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_216422.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Rv1352 (PF27111.1)
  • 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 COG1840
  • Curated reference: UniProt O07726 (TrEMBL, unreviewed; 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 — 57 functional partner(s); context anchor aao
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002021|Rv1906c|
MRLKPAPSPAAAFAVAGLILAGWAGSVGLAGADPEPAPTPKTAIDSDGTYAVGIDIAPGTYSSAGPVGDGTCYWKRMGNPDGALIDNALSKKPQVVTIEPTDKAFKTHGCQPWQNTGSEGAAPAGVPGPEAGAQLQNQLGILNGLLGPTGGRVPQP