echA15 Family assigned · medium auto-curated

H37Rv Rv2679 · MTBC0 mtbc0_002853 · 276 aa · 3017428–3018258 (+) · RefSeq NP_217195.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)enoyl-CoA hydratase EchA15
MTBC0 PGAP re-annotationenoyl-CoA hydratase/isomerase family protein
Revised (this work)Enoyl-CoA hydratase/isomerase family protein. Pfam: ECH_1 (PF00378.26), ECH_2 (PF16113.11).

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

Curated reference (UniProt)

UniProt I6YA03 TrEMBL · unreviewed · Evidence at protein level
UniProt nameProbable enoyl-CoA hydratase EchA15
Curated functionCould possibly oxidize fatty acids using specific components.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category I Lipid transport and metabolism
Preferred nameechA15
eggNOG descriptionBelongs to the enoyl-CoA hydratase isomerase family
Orthologous groupCOG1024
EC number EC 4.2.1.17
KEGG orthology K01692
KEGG pathways map00071, map00280, map00281, map00310, map00360, map00362, map00380, map00410, map00627, map00640, map00650, map00903, map00930, map01100, map01110, map01120, map01130, map01212
KEGG modules M00032, M00087

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 1.396 · diversifying/relaxed
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 4 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
ECH_1PF00378.26 9.5e-4022–267 Enoyl-CoA hydratase/isomerase
ECH_2PF16113.11 6.8e-1633–210 Enoyl-CoA hydratase/isomerase

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

Closest characterised functional partner: hemE (uroporphyrinogen decarboxylase), high confidence from genomic context alone (score 793 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv0400c fadE7 acyl-CoA dehydrogenase FadE7 851 846 database:750
Rv0154c fadE2 acyl-CoA dehydrogenase FadE2 850 845 database:750
Rv3140 fadE23 acyl-CoA dehydrogenase FadE23 859 844 database:750
Rv0131c fadE1 acyl-CoA dehydrogenase FadE1 850 844 database:750
Rv0231 fadE4 acyl-CoA dehydrogenase FadE4 850 844 database:750
Rv0975c fadE13 acyl-CoA dehydrogenase FadE13 850 844 database:750
Rv2500c fadE19 acyl-CoA dehydrogenase FadE19 849 844 database:750
Rv0468 fadB2 3-hydroxybutyryl-CoA dehydrogenase 815 808 database:650
Rv1715 fadB3 3-hydroxybutyryl-CoA dehydrogenase FadB 811 804 database:650
Rv2678c hemE uroporphyrinogen decarboxylase 792 793 ctx neighborhood:788
Rv2677c hemY protoporphyrinogen oxidase 790 791 ctx neighborhood:788
Rv2676c hemQ hyp hypothetical protein 790 791 ctx neighborhood:788
Rv2524c fas fatty acid synthase 816 789 coexpression:646
Rv1867 hyp hypothetical protein 782 782 database:447
Rv1627c nonspecific lipid-transfer protein 788 780 database:447

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: enoyl-CoA hydratase EchA15
  • MTBC0 PGAP product: enoyl-CoA hydratase/isomerase family protein
  • Pfam (hmmscan --cut_ga): ECH_1 PF00378.26 (E=1e-39), ECH_2 PF16113.11 (E=7e-16)
  • (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_217195.1)
  • Domains: Pfam-A via hmmscan --cut_ga — ECH_1 (PF00378.26), ECH_2 (PF16113.11)
  • 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 COG1024
  • Curated reference: UniProt I6YA03 (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 — 141 functional partner(s); context anchor hemE
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002853|Rv2679|echA15
MPVTYDDFPSLRCEIHDQPGHEGVLELVLDSPGLNSVGPHMHRDLADIWPVIDRDPAVRVVLVRGEGKAFSSGGSFDLIAETIGDYQGRLRIMREARDLVLNLVNFDKPVVSAIRGPAVGAGLVVALLADISVAGRAAKIIDGHTKLGVAAGDHAAICWPLLVGMAKAKYYLLTCEPLSGEEAERIGLVSICVDDDDVLPTATRLAERLAAGAQNAIRWTKRSLNHWYRMFGPAFETSLGLEFIGFGGPDVREGLAAHREKRPARFGADPDPGAGS