Rv2913c Family assigned · medium auto-curated

H37Rv Rv2913c · MTBC0 mtbc0_003095 · 611 aa · 3240692–3242527 (-) · RefSeq NP_217429.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)D-amino acid aminohydrolase
MTBC0 PGAP re-annotationamidohydrolase family protein
Revised (this work)Amidohydrolase family protein. Pfam: Amidohydro_3 (PF07969.18).

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

Curated reference (UniProt)

UniProt P9WJH9 SwissProt · reviewed · Evidence at protein level
UniProt nameUncharacterized protein Rv2913c

UniProt still lists this protein as Uncharacterized protein Rv2913c; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category Q Secondary metabolites biosynthesis, transport and catabolism
eggNOG descriptionN-acyl-D-aspartate D-glutamate deacylase
Orthologous groupCOG3653
Gene Ontology (8) GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0044424, GO:0044444, GO:0044464

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) pseudogene candidate

pN/pS 0.252 · purifying
Polymorphic sites (≥ 0.1% of strains) 11 synonymous, 7 missense, 1 nonsense, 2 frameshift
Disruption 3 distinct premature-stop/frameshift site(s); most common in 3.08% of strains (4466) · 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
Amidohydro_3PF07969.18 7.0e-1160–213 Amidohydrolase family

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

Closest characterised functional partner: Rv2912c (TetR family HTH-type transcriptional regulator), high confidence from genomic context alone (score 922 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2912c TetR family HTH-type transcriptional regulator 972 922 ctx neighborhood:881 textmining:653
Rv2914c pknI serine/threonine-protein kinase PknI 661 589 ctx neighborhood:588
Rv0293c hyp hypothetical protein 560 560 ctx cooccurence:558
Rv2916c ffh signal recognition particle protein 542 542 ctx neighborhood:540
Rv2915c hyp hypothetical protein 831 537 ctx neighborhood:537 textmining:650
Rv3775 lipE lipase LipE 497 498 ctx cooccurence:481
Rv1393c monoxygenase 423 424 ctx cooccurence:419
Rv1923 lipD lipase LipD 417 417
Rv1497 lipL esterase LipL 414 414
Rv2911 dacB2 penicillin-binding protein DacB2 471 96 textmining:439
Rv3330 dacB1 penicillin-binding protein DacB 466 93 textmining:436
Rv1367c hyp hypothetical protein 529 77 textmining:511
Rv3332 nagA N-acetylglucosamine-6-phosphate deacetylase NagA 674 51 textmining:671
Rv2970c lipN lipase/esterase LipN 522 48 textmining:519
Rv3451 cut3 cutinase 652 47 textmining:651

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: D-amino acid aminohydrolase
  • MTBC0 PGAP product: amidohydrolase family protein
  • Pfam (hmmscan --cut_ga): Amidohydro_3 PF07969.18 (E=7e-11)
  • (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_217429.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Amidohydro_3 (PF07969.18)
  • 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 COG3653
  • Curated reference: UniProt P9WJH9 (SwissProt, reviewed; 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 — 25 functional partner(s); context anchor Rv2912c
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003095|Rv2913c|
MLAWRQLNDLEETVTYDVIIRDGLWFDGTGNAPLTRTLGIRDGVVATVAAGALDETGCPEVVDAAGKWVVPGFIDVHTHYDAEVLLDPGLRESVRHGVTTVLLGNCSLSTVYANSEDAADLFSRVEAVPREFVLGALRDNQTWSTPAEYIEAIDALPLGPNVSSLLGHSDLRTAVLGLDRATDDTVRPTEAELAKMAKLLDEALEAGMLGMSGMDAAIDKLDGDRFRSRALPSTFATWRERRKLISVLRHRGRILQSAPDVDNPVSALLFFLASSRIFNRRKGVRMSMLVSADAKSMPLAVHVFGLGTRVLNKLLGSQVRFQHLPVPFELYSDGIDLPVFEEFGAGTAALHLRDQLQRNELLADRSYRRSFRREFDRIKLGPSLWHRDFHDAVIVECPDKSLIGKSFGAIADERGLHPLDAFLDVLVDNGERNVRWTTIVANHRPNQLNKLAAEPSVHMGFSDAGAHLRNMAFYNFGLRLLKRARDADRAGQPFLSIERAVYRLTGELAEWFGIGAGTLRQGDRADFAVIDPTHLDESVDGYHEEAVPYYGGLRRMVNRNDATVVATGVGGTVVFRGGQFGGQFRDGYGQNVKSGRYLRAGELGAALSRSA