Rv2766c Resolved · high auto-curated

H37Rv Rv2766c · MTBC0 - · 260 aa · 3075588–3076370 (-) · RefSeq YP_177905.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)short-chain type dehydrogenase/reductase
MTBC0 PGAP re-annotation
Revised (this work)Short-chain type dehydrogenase/reductase. Pfam: SDR (PF23441.1), adh_short (PF00106.32), KR (PF08659.17), adh_short_C2 (PF13561.13).

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 I6YEB6 TrEMBL · unreviewed · Evidence at protein level
UniProt nameProbable short-chain type dehydrogenase/reductase

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category I Lipid transport and metabolism
Q Secondary metabolites biosynthesis, transport and catabolism
eggNOG descriptionEnoyl-(Acyl carrier protein) reductase
Orthologous groupCOG1028

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 0.531 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 2 synonymous, 2 missense, 1 nonsense, 0 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.14% of strains (202) · 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
SDRPF23441.1 3.7e-116–246 SDR-like rossmann domain
adh_shortPF00106.32 3.7e-5010–198 short chain dehydrogenase
KRPF08659.17 1.0e-0610–162 KR domain
adh_short_C2PF13561.13 4.3e-5915–244 Enoyl-(Acyl carrier protein) reductase

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

Closest characterised functional partner: Rv2767c (membrane protein), high confidence from genomic context alone (score 784 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2524c fas fatty acid synthase 827 802 coexpression:509 experimental:475
Rv2767c membrane protein 784 784 ctx neighborhood:781
Rv1933c fadE18 acyl-CoA dehydrogenase FadE18 707 697 ctx neighborhood:544
Rv3761c fadE36 acyl-CoA dehydrogenase FadE36 703 692 ctx neighborhood:544
Rv1882c short-chain type dehydrogenase/reductase 681 682 ctx cooccurence:675
Rv0945 oxidoreductase 594 579 ctx cooccurence:520
Rv0148 short-chain type dehydrogenase/reductase 607 558 ctx cooccurence:557
Rv1937 oxygenase 593 546
Rv2243 fabD malonyl CoA-acyl carrier protein transacylase 552 536
Rv2299c htpG chaperone protein HtpG 545 525 database:450
Rv2564 glnQ glutamine ABC transporter ATP-binding protein 536 515 database:431
Rv0073 glutamine ABC transporter ATP-binding protein 532 510 database:431
Rv3728 membrane protein 534 509 database:431
Rv3239c transmembrane transport protein 532 507 database:431
Rv2565 NTE family protein 521 502 database:431

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): short-chain type dehydrogenase/reductase
  • Pfam (hmmscan --cut_ga): SDR PF23441.1 (E=4e-11), adh_short PF00106.32 (E=4e-50), KR PF08659.17 (E=1e-06), adh_short_C2 PF13561.13 (E=4e-59)
  • (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 YP_177905.1)
  • Domains: Pfam-A via hmmscan --cut_ga — SDR (PF23441.1), adh_short (PF00106.32), KR (PF08659.17), adh_short_C2 (PF13561.13)
  • 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 COG1028
  • Curated reference: UniProt I6YEB6 (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 — 78 functional partner(s); context anchor Rv2767c
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv2766c|
MTSLDLTGRTAIITGASRGIGLAIAQQLAAAGAHVVLTARRQEAADEAAAQVGDRALGVGAHAVDEDAARRCVDLTLERFGSVDILINNAGTNPAYGPLLEQDHARFAKIFDVNLWAPLMWTSLVVTAWMGEHGGAVVNTASIGGMHQSPAMGMYNATKAALIHVTKQLALELSPRIRVNAICPGVVRTRLAEALWKDHEDPLAATIALGRIGEPADIASAVAFLVSDAASWITGETMIIDGGLLLGNALGFRAAPSTEH