Rv1577c Resolved · high auto-curated

H37Rv Rv1577c · MTBC0 - · 170 aa · 1782072–1782584 (-) · RefSeq NP_216093.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)phage prohead protease
MTBC0 PGAP re-annotation
Revised (this work)Phage prohead protease. Pfam: Peptidase_S78 (PF04586.23).

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

Annotated on the H37Rv protein: this gene has no 1:1 ancestral MTBC0 anchor (PE/PPE, paralogue, IS element, or otherwise unanchored CDS).

Curated reference (UniProt)

UniProt O06613 TrEMBL · unreviewed · Predicted
UniProt nameProbable PhiRv1 phage protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
eggNOG descriptionCaudovirus prohead serine protease
Orthologous groupCOG3740
KEGG orthology K06904

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
Peptidase_S78PF04586.23 1.2e-199–153 Caudovirus prohead serine protease

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

Closest characterised functional partner: Rv1576c (phage capsid protein), high confidence from genomic context alone (score 988 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1576c phage capsid protein 988 988 ctx neighborhood:787 cooccurence:675 coexpression:838
Rv2650c prophage protein 955 952 ctx cooccurence:693 coexpression:839
Rv2651c prophage protease 848 847 coexpression:846
Rv1578c phage protein 665 646 ctx neighborhood:478
Rv1452c PE_PGRS28 PE-PGRS family protein PE_PGRS28 609 609 ctx cooccurence:604
Rv3350c PPE56 PPE family protein PPE56 590 590 ctx cooccurence:586
Rv0355c PPE8 PPE family protein PPE8 585 586 ctx cooccurence:583
Rv3347c PPE55 PPE family protein PPE55 582 582 ctx cooccurence:578
Rv2490c PE_PGRS43 PE-PGRS family protein PE_PGRS43 577 578 ctx cooccurence:572
Rv0304c PPE5 PPE family protein PPE5 550 551 ctx cooccurence:548
Rv3343c PPE54 PPE family protein PPE54 540 540 ctx cooccurence:536
Rv0872c PE_PGRS15 PE-PGRS family protein PE_PGRS15 539 539 ctx cooccurence:533
Rv1004c membrane protein 538 539 ctx cooccurence:536
Rv1749c integral membrane protein 533 533 ctx cooccurence:532
Rv1917c PPE34 PPE family protein PPE34 532 532 ctx cooccurence:531

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

  • Annotation from H37Rv (no MTBC0 1:1 anchor; H37Rv protein used): phage prohead protease
  • Pfam (hmmscan --cut_ga): Peptidase_S78 PF04586.23 (E=1e-19)
  • (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_216093.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Peptidase_S78 (PF04586.23)
  • 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 COG3740
  • Curated reference: UniProt O06613 (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 — 45 functional partner(s); context anchor Rv1576c
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv1577c|
MAELRSGEGRTVHGTIVPYNEATTVRDFDGEFQEMFAPGAFRRSIAERGHKLKLLVSHDARTRYPVGRAVELREEPHGLFGAFEIADTPDGDEALANVKAGVVDSFSVGFRPIRDRREGDVLVRVEAALLEVSLTGVPAYSGAQIAGVRAESLTVVSRSTAEAWLSLLDW