Rv2672 Resolved · high auto-curated

H37Rv Rv2672 · MTBC0 mtbc0_002846 · 528 aa · 3009885–3011471 (+) · RefSeq NP_217188.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)protease
MTBC0 PGAP re-annotationalpha/beta fold hydrolase
Revised (this work)Alpha/beta fold hydrolase. Pfam: Abhydrolase_1 (PF00561.27), Abhydrolase_4 (PF08386.17).

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

Curated reference (UniProt)

UniProt P71969 TrEMBL · unreviewed · Evidence at protein level
UniProt namePossible secreted protease

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
eggNOG descriptionAlpha beta hydrolase
Orthologous groupCOG0596

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 0.616 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 4 synonymous, 7 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
Abhydrolase_1PF00561.27 1.9e-09160–313 alpha/beta hydrolase fold
Abhydrolase_4PF08386.17 3.3e-21424–526 TAP-like protein

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

Closest characterised functional partner: aftC (alpha-(1->3)-arabinofuranosyltransferase), high confidence from genomic context alone (score 909 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2673 aftC alpha-(1->3)-arabinofuranosyltransferase 909 909 ctx neighborhood:849 cooccurence:414
Rv1275 lprC lipoprotein LprC 767 768 ctx cooccurence:755
Rv3035 hyp hypothetical protein 756 757 ctx cooccurence:745
Rv0817c lmeA hyp hypothetical protein 750 751 ctx cooccurence:750
Rv2674 msrB peptide methionine sulfoxide reductase MsrB 748 749 ctx neighborhood:747
Rv1274 lprB lipoprotein LprB 748 749 ctx cooccurence:745
Rv3244c lpqB lipoprotein LpqB 737 738 ctx cooccurence:736
Rv0466 hyp hypothetical protein 714 715 ctx cooccurence:713
Rv0383c ttfA hyp hypothetical protein 713 713 ctx cooccurence:713
Rv0290 eccD3 ESX-3 secretion system protein EccD 699 700 ctx cooccurence:699
Rv2671 ribD bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase 724 664 ctx neighborhood:659
Rv1125 hyp hypothetical protein 663 664 ctx cooccurence:662
Rv3668c protease 653 653 ctx cooccurence:649
Rv1109c hyp hypothetical protein 648 648 ctx cooccurence:645
Rv3910 murJ peptidoglycan biosynthesis protein 642 643 ctx cooccurence:628

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: protease
  • MTBC0 PGAP product: alpha/beta fold hydrolase
  • Pfam (hmmscan --cut_ga): Abhydrolase_1 PF00561.27 (E=2e-09), Abhydrolase_4 PF08386.17 (E=3e-21)
  • (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_217188.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Abhydrolase_1 (PF00561.27), Abhydrolase_4 (PF08386.17)
  • 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 COG0596
  • Curated reference: UniProt P71969 (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 — 125 functional partner(s); context anchor aftC
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002846|Rv2672|
MATVVGMSRPMTSTAMLVALTCSATVLAACVPAFGADPRFATYSGAGPQGAATTTPPPAGPPPLAAPKNDLSWHDCTSRVYSNAGIPAAPGVKLECASYDTDLDPLVGGSTAVSIGVVRARSNQTPSDAGPLVFTTGSDLPSSTQLPVWLAHAGIDVLRSHPIVAVDRRGMGMSSPIDCRDHFDRDEMRDQAQFQAGDDPVANLSDISNTATTDCTDAIAPGESAYDNTHAASDIERLRKLWDVPALAFVGIGNGTQVALAYAASRPDNVARLILDSPIALGVSAEAAAEQQVQGQQAALDAFAAQCVAVNCALGSDPKGAVSALLSAARSGDGPGGASVAAVANAVATALGFPDSGRVDSTTKLADALAAARSGDMNLLSALINRADTTRDTDGQFISSCSDAVNRPTPDRVRELVVAWGKLYPQFGAVAALNLVKCVHWPSSSPPQPPKDLKVDVLLLGVQNDPIVGNEGVAATAATAINANAASKRVMWQGIGHGASIYSSCAVPPLVAYLDTGKLPDTDTYCPA