Rv1524 Resolved · high auto-curated

H37Rv Rv1524 · MTBC0 mtbc0_001631 · 414 aa · 1728535–1729779 (+) · RefSeq NP_216040.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)glycosyltransferase
MTBC0 PGAP re-annotationglycosyltransferase
Revised (this work)Glycosyltransferase. Pfam: Glyco_transf_28 (PF03033.27), EryCIII-like_C (PF06722.19).

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

Curated reference (UniProt)

UniProt P9WN07 SwissProt · reviewed · Evidence at protein level
UniProt nameUncharacterized glycosyltransferase Rv1524
EC (curated) EC 2.4.-.-

UniProt still lists this protein as Uncharacterized glycosyltransferase Rv1524; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category C Energy production and conversion
G Carbohydrate transport and metabolism
eggNOG descriptionCOG1819 Glycosyl transferases, related to UDP-glucuronosyltransferase
Orthologous groupCOG1819
EC number EC 2.4.1.173
KEGG orthology K05841
CAZy family GT1
Gene Ontology (14) GO:0003674, GO:0003824, GO:0005575, GO:0005622, GO:0005623, GO:0008194, GO:0016740, GO:0016757, GO:0043226, GO:0043227, GO:0043229, GO:0043231 +2 more

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 0.16 · strong purifying
Polymorphic sites (≥ 0.1% of strains) 11 synonymous, 5 missense, 0 nonsense, 2 frameshift
Disruption 2 distinct premature-stop/frameshift site(s); most common in 0.24% of strains (350) · 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
Glyco_transf_28PF03033.27 1.9e-083–84 Glycosyltransferase family 28 N-terminal domain
EryCIII-like_CPF06722.19 2.3e-13295–396 Erythromycin biosynthesis protein CIII-like, C-terminal domain

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

Closest characterised functional partner: Rv1523 (methyltransferase), high confidence from genomic context alone (score 898 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1523 methyltransferase 898 898 ctx neighborhood:721 coexpression:651
Rv1525 wbbL2 rhamnosyl transferase WbbL 751 742 ctx neighborhood:670
Rv1182 papA3 acyltransferase papA3 636 621 ctx cooccurence:608
Rv3824c papA1 acyltransferase 627 612 ctx cooccurence:600
Rv3820c papA2 trehalose-2-sulfate acyltransferase 619 603 ctx cooccurence:589
Rv1522c mmpL12 transmembrane transport protein MmpL12 526 509 ctx neighborhood:497
Rv0295c stf0 hyp hypothetical protein 498 499 ctx cooccurence:493
Rv0764c cyp51 lanosterol 14-alpha demethylase 489 477
Rv1851 ureF urease accessory protein UreF 421 422 ctx cooccurence:413
Rv0063 oxidoreductase 421 422
Rv1181 pks4 polyketide beta-ketoacyl synthase 430 402
Rv2226 hyp hypothetical protein 400 401
Rv2946c pks1 polyketide synthase 406 372
Rv0519c membrane protein 403 372
Rv3351c hyp hypothetical protein 902 277 textmining:870

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: glycosyltransferase
  • MTBC0 PGAP product: glycosyltransferase
  • Pfam (hmmscan --cut_ga): Glyco_transf_28 PF03033.27 (E=2e-08), EryCIII-like_C PF06722.19 (E=2e-13)
  • (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_216040.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Glyco_transf_28 (PF03033.27), EryCIII-like_C (PF06722.19)
  • 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 COG1819
  • Curated reference: UniProt P9WN07 (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 — 24 functional partner(s); context anchor Rv1523
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001631|Rv1524|
MKFVVASYGTRGDIEPCAAVGLELQRRGHDVCLAVPPNLIGFVETAGLSAVAYGSRDSQEQLDEQFLHNAWKLQNPIKLLREAMAPVTEGWAELSAMLTPVAAGADLLLTGQIYQEVVANVAEHHGIPLAALHFYPVRANGEIAFPARLPAPLVRSTITAIDWLYWRMTKGVEDAQRRELGLPKASTPAPRRMAVRGSLEIQAYDALCFPGLAAEWGGRRPFVGALTMESATDADDEVASWIAADTPPIYFGFGSMPIGSLADRVAMISAACAELGERALICSGPSDATGIPQFDHVKVVRVVSHAAVFPTCRAVVHHGGAGTTAAGLRAGIPTLILWVTSDQPIWAAQIKQLKVGRGRRFSSATKESLIADLRTILAPDYVTRAREIASRMTKPAASVTATADLLEDAARRAR