Rv2655c Still unknown · low auto-curated

H37Rv Rv2655c · MTBC0 mtbc0_002829 · 475 aa · 2999434–3000861 (-) · RefSeq NP_217171.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)prophage protein
MTBC0 PGAP re-annotationDUF3631 domain-containing protein
Revised (this work)Conserved hypothetical protein; DUF domain(s) DUF3631. Function unknown.

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

Curated reference (UniProt)

UniProt I6Y1F0 TrEMBL · unreviewed · Predicted
UniProt namePossible PhiRv2 prophage protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category O Post-translational modification, protein turnover, chaperones
eggNOG descriptionProtein of unknown function (DUF3631)
Orthologous groupCOG0464

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 0.796 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 7 missense, 0 nonsense, 1 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.40% of strains (585) · clonal

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
DUF3631PF12307.14 2.1e-61195–375 Protein of unknown function (DUF3631)

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

Closest characterised functional partner: Rv2656c (prophage protein), high confidence from genomic context alone (score 830 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2656c prophage protein 831 830 ctx neighborhood:799
Rv2659c prophage integrase 819 819 ctx neighborhood:746
Rv2657c prophage protein 800 800 ctx neighborhood:798
Rv2654c antitoxin 784 784 ctx neighborhood:781
Rv2658c prophage protein 747 748 ctx neighborhood:746
Rv2653c toxin 585 586 ctx neighborhood:567
Rv2652c prophage protein 513 512 ctx neighborhood:504
Rv2660c hyp hypothetical protein 469 469 ctx neighborhood:461
Rv2661c hyp hypothetical protein 464 464 ctx neighborhood:461
Rv3578 arsB2 arsenic transport integral membrane protein ArsB 440 441 ctx cooccurence:437
Rv3875 esxA ESAT-6 protein EsxA 422 423 ctx cooccurence:421
Rv3660c ssd hyp hypothetical protein 421 421 ctx cooccurence:416
Rv2650c prophage protein 402 371
Rv2896c dprA hyp hypothetical protein 655 51 textmining:652
Rv1014c pth peptidyl-tRNA hydrolase 570 46 textmining:568

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: prophage protein
  • MTBC0 PGAP product: DUF3631 domain-containing protein
  • Pfam (hmmscan --cut_ga): DUF3631 PF12307.14 (E=2e-61)
  • (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_217171.1)
  • Domains: Pfam-A via hmmscan --cut_ga — DUF3631 (PF12307.14)
  • 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 COG0464
  • Curated reference: UniProt I6Y1F0 (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 — 19 functional partner(s); context anchor Rv2656c
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002829|Rv2655c|
MADIPYGRDYPDPIWCDEDGQPMPPVGAELLDDIRAFLRRFVVYPSDHELIAHTLWIAHCWFMEAWDSTPRIAFLSPEPGSGKSRALEVTEPLVPRPVHAINCTPAYLFRRVADPVGRPTVLYDECDTLFGPKAKEHEEIRGVINAGHRKGAVAGRCVIRGKIVETEELPAYCAVALAGLDDLPDTIMSRSIVVRMRRRAPTEPVEPWRPRVNGPEAEKLHDRLANWAAAINPLESGWPAMPDGVTDRRADVWESLVAVADTAGGHWPKTARATAETDATANRGAKPSIGVLLLRDIRRVFSDRDRMRTSDILTGLNRMEEGPWGSIRRGDPLDARGLATRLGRYGIGPKFQHSGGEPPYKGYSRTQFEDAWSRYLSADDETPEERDLSVSAVSAVSPPVGDPGDATGATDATDLPEAGDLPYEPPAPNGHPNGDAPLCSGPGCPNKLLSTEAKAAGKCRPCRGRAAASARDGAR