ilvE Resolved · high auto-curated

H37Rv Rv2210c · MTBC0 mtbc0_002346 · 368 aa · 2501021–2502127 (-) · RefSeq NP_216726.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)branched-chain amino acid aminotransferase
MTBC0 PGAP re-annotationbranched-chain amino acid aminotransferase
Revised (this work)Branched-chain amino acid aminotransferase. Pfam: Aminotran_4 (PF01063.25).

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

Curated reference (UniProt)

UniProt P9WQ75 SwissProt · reviewed · Evidence at protein level
UniProt nameBranched-chain-amino-acid aminotransferase
EC (curated) EC 2.6.1.42
Curated functionCatalyzes the reversible transfers of an amino group from glutamate to the alpha-ketoacid of the respective amino acid in the final step in the biosynthesis of branchedchain amino acids. The amino acids can be ranked in the following order with respect to their efficiency as amino donor: Leu > Ile > Val.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category E Amino acid transport and metabolism
Preferred nameilvE
eggNOG descriptionBranched-chain amino acid aminotransferase
Orthologous groupCOG0115
EC number EC 2.6.1.42
KEGG orthology K00826
KEGG pathways map00270, map00280, map00290, map00770, map01100, map01110, map01130, map01210, map01230
KEGG modules M00019, M00036, M00119, M00570
Gene Ontology (69) GO:0000096, GO:0000097, GO:0003674, GO:0003824, GO:0004084, GO:0005488, GO:0006082, GO:0006464, GO:0006520, GO:0006555, GO:0006790, GO:0006807 +57 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 0.431 · purifying
Polymorphic sites (≥ 0.1% of strains) 4 synonymous, 5 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
Aminotran_4PF01063.25 1.2e-2776–323 Amino-transferase class IV

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

Closest characterised functional partner: gcvT (aminomethyltransferase), high confidence from genomic context alone (score 797 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv0189c ilvD dihydroxy-acid dehydratase 994 982 coexpression:669 database:900 textmining:736
Rv3710 leuA 2-isopropylmalate synthase 987 965 coexpression:608 database:900 textmining:662
Rv1079 metB cystathionine gamma-synthase 972 917 database:900 textmining:682
Rv0337c aspC aspartate aminotransferase 911 906 database:900
Rv2225 panB 3-methyl-2-oxobutanoate hydroxymethyltransferase 916 904 database:900
Rv3704c gshA glutamate--cysteine ligase 900 901 database:900
Rv1559 ilvA threonine dehydratase IlvA 974 886 coexpression:421 database:800 textmining:784
Rv1294 thrA homoserine dehydrogenase 926 884 coexpression:412 database:800
Rv1296 thrB homoserine kinase 866 827 database:800
Rv2211c gcvT aminomethyltransferase 820 797 ctx neighborhood:792
Rv2212 adenylyl cyclase 730 730 ctx neighborhood:730
Rv2213 pepB cytosol aminopeptidase 744 728 ctx neighborhood:726
Rv3534c hsaF 4-hydroxy-2-oxovalerate aldolase 682 662 coexpression:607
Rv3469c mhpE 4-hydroxy-2-oxovalerate aldolase MhpE 681 661 coexpression:606
Rv2496c bkdB 3-methyl-2-oxobutanoate dehydrogenase subunit beta 831 625 database:500 textmining:569

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: branched-chain amino acid aminotransferase
  • MTBC0 PGAP product: branched-chain amino acid aminotransferase
  • Pfam (hmmscan --cut_ga): Aminotran_4 PF01063.25 (E=1e-27)
  • (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_216726.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Aminotran_4 (PF01063.25)
  • 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 COG0115
  • Curated reference: UniProt P9WQ75 (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 — 55 functional partner(s); context anchor gcvT
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002346|Rv2210c|ilvE
MTSGSLQFTVLRAVNPATDAQRESMLREPGFGKYHTDHMVSIDYAEGRGWHNARVIPYGPIELDPSAIVLHYAQEVFEGLKAYRWADGSIVSFRADANAARLRSSARRLAIPELPDAVFIESLRQLIAVDKAWVPGAGGEEALYLRPFIFATEPGLGVRPATQYRYLLIASPAGAYFKGGIAPVSVWVSTEYVRACPGGTGAAKFGGNYAASLLAQAEAAENGCDQVVWLDAVERRYIEEMGGMNIFFVLGSGGSARLVTPELSGSLLPGITRDSLLQLAIDAGFAVEERRIDIDEWQKKAAAGEITEVFACGTAAVITPVARVRHGASEFRIADGQPGEVTMALRDTLTGIQRGTFADTHGWMARLG