Rv1075c Family assigned · medium auto-curated

H37Rv Rv1075c · MTBC0 mtbc0_001155 · 314 aa · 1207695–1208639 (-) · RefSeq NP_215591.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationSGNH/GDSL hydrolase family protein
Revised (this work)SGNH/GDSL hydrolase family protein. Pfam: Lipase_GDSL (PF00657.29), Lipase_GDSL_2 (PF13472.13).

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

Curated reference (UniProt)

UniProt O53423 SwissProt · reviewed · Evidence at protein level
UniProt nameGDSL-like esterase Rv1075c
EC (curated) EC 3.1.-.-, EC 3.1.1.6
Curated functionEsterase that preferentially hydrolyzes short-chain fatty acids, particularly pNP-acetate (C2) and pNP-butyrate (C4). Also has weak activity with pNP-hexanoate (C6) and pNP-octanoate (C8). It can also hydrolyze short-chain tryglycerides such as triacetin and tributyrin. Important for intracellular survival.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category E Amino acid transport and metabolism
eggNOG descriptionGDSL-like Lipase/Acylhydrolase family
Orthologous groupCOG2755

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 0.593 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 4 synonymous, 6 missense, 0 nonsense, 1 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.60% of strains (873) · 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
Lipase_GDSLPF00657.29 2.2e-1074–259 GDSL-like Lipase/Acylhydrolase
Lipase_GDSL_2PF13472.13 2.6e-1976–255 GDSL-like Lipase/Acylhydrolase family

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

Closest characterised functional partner: fadA3 (beta-ketoacyl CoA thiolase FadA), high confidence from genomic context alone (score 812 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv1074c fadA3 beta-ketoacyl CoA thiolase FadA 935 812 ctx neighborhood:811 textmining:670
Rv0048c membrane protein 715 716 ctx cooccurence:649
Rv1076 lipU lipase LipU 718 706 ctx neighborhood:614
Rv0756c hyp hypothetical protein 571 551 experimental:425
Rv3662c hyp hypothetical protein 534 534 ctx cooccurence:521
Rv1171 hyp hypothetical protein 511 512 ctx cooccurence:510
Rv1950c hyp hypothetical protein 500 476 experimental:425
Rv0909 antitoxin 498 474 experimental:425
Rv3903c cpnT hyp hypothetical protein 497 473 experimental:425
Rv3881c espB ESX-1 secretion-associated protein EspB 496 472 experimental:425
Rv3773c hyp hypothetical protein 463 463 ctx cooccurence:463
Rv1987 chitinase 493 461 experimental:405
Rv3202c adnA ATP-dependent DNA helicase 460 461
Rv0822c hyp hypothetical protein 479 456 ctx cooccurence:453
Rv0648 alpha-mannosidase 455 456 ctx cooccurence:444

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: hypothetical protein
  • MTBC0 PGAP product: SGNH/GDSL hydrolase family protein
  • Pfam (hmmscan --cut_ga): Lipase_GDSL PF00657.29 (E=2e-10), Lipase_GDSL_2 PF13472.13 (E=3e-19)
  • (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_215591.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Lipase_GDSL (PF00657.29), Lipase_GDSL_2 (PF13472.13)
  • 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 COG2755
  • Curated reference: UniProt O53423 (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 — 38 functional partner(s); context anchor fadA3
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001155|Rv1075c|
MPRRSTIALATAGALASTGTAYLGARNLLVGQATHARTVIPKSFDAPPRADGVYTRGGGPVQRWRREVPFDVHLMIFGDSTATGYGCASAEEVPGVLIARGLAEQTGKRIRLSTKAIVGATSKGVCGQVDAMFVVGPPPDAAVIMIGANDITALNGIGPSAQRLADCVRRLRTRGAVVVVGTCPDLGVITAIPQPLRALAHTRGVRLARAQTAAVKAAGGVPVPLGHLLAPKFRAMPELMFSADRYHPSAPAYALAADLLFLALRDALTEKLDIPIHETPSRPGTATLEPGHTRHSMMSRLRRPRPARAVPTGG