Rv1230c Family assigned · medium auto-curated

H37Rv Rv1230c · MTBC0 mtbc0_001319 · 411 aa · 1381406–1382641 (-) · RefSeq NP_215746.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)membrane protein
MTBC0 PGAP re-annotationlytic transglycosylase domain-containing protein
Revised (this work)Lytic transglycosylase domain-containing protein. Pfam: SLT_2 (PF13406.12).

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

Curated reference (UniProt)

UniProt O86313 TrEMBL · unreviewed · Predicted
UniProt namePossible membrane protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category M Cell wall / membrane / envelope biogenesis
eggNOG descriptionTransglycosylase SLT domain
Orthologous groupCOG2951

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 4.486 · diversifying/relaxed
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 12 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
SLT_2PF13406.12 9.6e-08194–249 Transglycosylase SLT domain

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

Closest characterised functional partner: mrp (multiple resistance/pH adaptation protein), high confidence from genomic context alone (score 809 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1229c mrp multiple resistance/pH adaptation protein 809 809 ctx neighborhood:803
Rv1231c membrane protein 913 762 ctx neighborhood:761 textmining:653
Rv1232c hyp hypothetical protein 762 762 ctx neighborhood:761
Rv3594 hyp hypothetical protein 704 685 ctx cooccurence:683
Rv2164c hyp hypothetical protein 588 588 ctx cooccurence:572
Rv3365c hyp hypothetical protein 541 528 ctx cooccurence:525
Rv1233c hyp hypothetical protein 513 513 ctx neighborhood:510
Rv3201c adnB ATP-dependent DNA helicase 510 511 ctx cooccurence:495
Rv2542 hyp hypothetical protein 486 486 ctx cooccurence:484
Rv0345 hyp hypothetical protein 474 474 ctx cooccurence:448
Rv3877 eccD1 ESX-1 secretion system protein EccD1 458 458 ctx cooccurence:458
Rv3869 eccB1 ESX-1 secretion system protein EccB 453 454 ctx cooccurence:447
Rv0867c rpfA resuscitation-promoting factor RpfA 444 445 ctx cooccurence:425
Rv1226c transmembrane protein 443 444 ctx cooccurence:442
Rv0192 hyp hypothetical protein 435 435 ctx cooccurence:428

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: membrane protein
  • MTBC0 PGAP product: lytic transglycosylase domain-containing protein
  • Pfam (hmmscan --cut_ga): SLT_2 PF13406.12 (E=1e-07)
  • (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_215746.1)
  • Domains: Pfam-A via hmmscan --cut_ga — SLT_2 (PF13406.12)
  • 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 COG2951
  • Curated reference: UniProt O86313 (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 — 29 functional partner(s); context anchor mrp
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001319|Rv1230c|
MHIGGRWGARPAVAAVRRGACRLTRAPAFGVAAIAPLVFASAVGGAAPVFPGRTAPVHAVITPVAAVAASGIDLSGPVVIAMKRPPTSFRVAVATISAPPPPMIVNSPGALGIPAMALSAYRNAELKMAAAAPGCGVSWNLLAGIGRIESMHANGGATDARGTAIQPIYGPTLDGTLPGNEIIIQSSVGNRVTYARAMGPMQFLPGTWARYATDGDDDGVADPQNLFDSTLAAARYLCSGGLNLRDPAQVMAALLRYNNSMPYAQNVLGWAAGYATGVFPVDLPPITGPPPPLGDAHLENPEGLGPGLPINVNGLTADGPMAHLPLIDLTPRQAALNPPPMFPWMAPDPSAPMPGCTLICIGSHGPPVGAPPFPPTAPPPPFLPAAPPPPDPLAGPPGDAGLAPPAPAPAG