Rv1085c Family assigned · medium auto-curated

H37Rv Rv1085c · MTBC0 mtbc0_001165 · 242 aa · 1218025–1218753 (-) · RefSeq NP_215601.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hemolysin-like protein
MTBC0 PGAP re-annotationhemolysin III family protein
Revised (this work)Hemolysin III family protein. Pfam: HlyIII (PF03006.27).

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

Curated reference (UniProt)

UniProt P9WFN7 SwissProt · reviewed · Inferred from homology
UniProt nameUPF0073 membrane protein Rv1085c

UniProt still lists this protein as UPF0073 membrane protein Rv1085c; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
Preferred namehlyI
eggNOG descriptionprotein, hemolysin III
Orthologous groupCOG1272
KEGG orthology K11068

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, 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
HlyIIIPF03006.27 9.4e-5231–234 Haemolysin-III related

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

Closest characterised functional partner: Rv1086 ((2Z,6E)-farnesyl diphosphate synthase), medium confidence from genomic context alone (score 596 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1086 (2Z,6E)-farnesyl diphosphate synthase 595 596 ctx neighborhood:596
Rv3696c glpK glycerol kinase 605 554 database:546
Rv1770 hyp hypothetical protein 532 532 database:532
Rv0418 lpqL lipoprotein aminopeptidase LpqL 532 532 database:532
Rv3884c eccA2 ESX-2 secretion system protein EccA 476 477 database:475
Rv0282 eccA3 ESX-3 secretion system protein EccA 476 477 database:475
Rv3868 eccA1 ESX-1 secretion system protein EccA1 476 477 database:475
Rv0435c ATPase 476 477 database:475
Rv3211 rhlE ATP-dependent RNA helicase RhlE 446 426
Rv1329c dinG ATP-dependent helicase DinG 414 415 database:404
Rv3537 kstD 3-oxosteroid 1-dehydrogenase 413 414
Rv3318 sdhA succinate dehydrogenase flavoprotein subunit 413 414
Rv0248c succinate dehydrogenase flavoprotein subunit 413 414
Rv1817 flavoprotein 413 414
Rv1552 frdA fumarate reductase flavoprotein subunit 413 414

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: hemolysin-like protein
  • MTBC0 PGAP product: hemolysin III family protein
  • Pfam (hmmscan --cut_ga): HlyIII PF03006.27 (E=9e-52)
  • (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_215601.1)
  • Domains: Pfam-A via hmmscan --cut_ga — HlyIII (PF03006.27)
  • 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 COG1272
  • Curated reference: UniProt P9WFN7 (SwissProt, reviewed; Inferred from homology)
  • 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 — 28 functional partner(s); context anchor Rv1086
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001165|Rv1085c|
MSGQADTATTAEARTPAHAAHHLVEGVARVLTKPRFRGWIHVYSAGTAVLAGASLVAVSWAVGSAKAGLTTLAYTAATITMFTVSATYHRVNWKSATARNWMKRADHSMIFVFIAGSYTPFALLALPAHDGRVVLSIVWGGAIAGILLKMCWPAAPRSVGVPLYLLLGWVAVWYTATILHNAGVTALVLLFVGGALYSIGGILYAVRWPDPWPTTFGYHEFFHACTAVAAICHYIAMWFVVF