bglS Resolved · high auto-curated

H37Rv Rv0186 · MTBC0 - · 691 aa · 216269–218344 (+) · RefSeq NP_214700.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)beta-glucosidase BglS
MTBC0 PGAP re-annotation
Revised (this work)Beta-glucosidase BglS. Pfam: Glyco_hydro_3 (PF00933.28), Glyco_hydro_3_C (PF01915.28), Fn3-like (PF14310.13).

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 O07430 TrEMBL · unreviewed · Evidence at protein level
UniProt nameProbable beta-glucosidase BglS

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category G Carbohydrate transport and metabolism
Preferred namebglS
eggNOG descriptionFibronectin type III-like domain
Orthologous groupCOG1472
EC number EC 3.2.1.21
KEGG orthology K05349
KEGG pathways map00460, map00500, map00940, map01100, map01110
CAZy family GH3

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 0.348 · purifying
Polymorphic sites (≥ 0.1% of strains) 12 synonymous, 11 missense, 1 nonsense, 3 frameshift
Disruption 4 distinct premature-stop/frameshift site(s); most common in 0.63% of strains (916) · convergent

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_hydro_3PF00933.28 2.4e-3543–292 Glycosyl hydrolase family 3 N terminal domain
Glyco_hydro_3_CPF01915.28 5.2e-56325–574 Glycosyl hydrolase family 3 C-terminal domain
Fn3-likePF14310.13 8.5e-17607–673 Fibronectin type III-like domain

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

Closest characterised functional partner: galK (galactokinase), medium confidence from genomic context alone (score 572 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2471 aglA alpha-glucosidase AglA 945 922 database:900
Rv0185 hyp hypothetical protein 916 917 ctx neighborhood:652 coexpression:770
Rv0062 celA1 cellulase CelA 981 902 database:900 textmining:819
Rv1090 celA2b Rv1090, (MTV017.43), len: 151 aa. Probable celA2b,second part of cellulase (endoglucanase), similar to C-terminus of others e.g. O08468 cell 981 902 database:900 textmining:819
Rv1089A celA2a Rv1089A, len: 34 aa. Probable celA2a, first part of cellulase (endoglucanase), similar to N-terminus of others. This region is a possible MT 900 901 database:900
Rv0184 hyp hypothetical protein 713 713 ctx neighborhood:652
Rv0620 galK galactokinase 571 572 ctx cooccurence:561
Rv3575c LacI family transcriptional regulator 591 566 ctx cooccurence:551
Rv0183 lysophospholipase 557 537 ctx neighborhood:537
Rv0729 xylB D-xylulose kinase XylB 504 473 ctx cooccurence:409
Rv0182c sigG ECF RNA polymerase sigma factor SigG 437 437 ctx neighborhood:419
Rv3242c hyp hypothetical protein 436 437 coexpression:433
Rv0181c hyp hypothetical protein 400 401
Rv0212c nadR transcriptional regulator NadR 404 191
Rv3096 hyp hypothetical protein 882 99 textmining:875

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): beta-glucosidase BglS
  • Pfam (hmmscan --cut_ga): Glyco_hydro_3 PF00933.28 (E=2e-35), Glyco_hydro_3_C PF01915.28 (E=5e-56), Fn3-like PF14310.13 (E=9e-17)
  • (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_214700.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Glyco_hydro_3 (PF00933.28), Glyco_hydro_3_C (PF01915.28), Fn3-like (PF14310.13)
  • 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 COG1472
  • Curated reference: UniProt O07430 (TrEMBL, unreviewed; 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 — 21 functional partner(s); context anchor galK
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv0186|bglS
MTDDERFSLLVGLTGASDLWPVRDERIPQGVPMCAGYVPGIPRLGVPALLMSDAGLGVTNPGYRPGDTATALPAGLALAASFNPVLARSSGKAIGREARSRGFNVQLAGAINLARDPRNGRNFEYLSEDPLLSATMAAESIIGIQQQGVIATTKHFSLNCNETNRHWLDAVIDPDAHRESDLLAFEIVIERSQPGAVMAAYNKVNGDYAAGNDHLLNDVLKGAWGYRGWVMSDWGGTPSWECALAGLDQECGAQIDAVLWQSEAFTDRLRAAYADGNLPKGRLSDMVRRILRSMFAVGIDRWKPAPAPDMNAHNEIAAQMARQGIVLLQNRGLLPLAPESAGRIAVIGGYAHLGVPAGYGSSAVTPPGGYAGVIPIGGSGLAAGLRNLYLLPSSPLSELRKRLPNAQFEFDPGINPAEAVLAARRADIAIVFAIRAEGEGFDSADLSLPWGQDALIAAVASANANTVVVLETGNPVTMPWRDSVNAIMQAWYPGQAGGQAVAEIVTGQVNPSGRLPITFPVDLGQTPRSQPPELGAPWGTSTTIHYTEGADVGYRWFASTNQTPMFAFGHGLSYTSFEYRDLVVTGGHTVHASFSVTNTGDRSGADVPQLYMIAAPGESRLRLLGFERVELEPGQTRRVRIEADPRLLARYDGEARSWRIEPGGYTVAVGASAVALKLAAKVKLAGRGFGR