icd2 Resolved · high auto-curated

H37Rv Rv0066c · MTBC0 mtbc0_000073 · 745 aa · 72419–74656 (-) · RefSeq NP_214580.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)isocitrate dehydrogenase
MTBC0 PGAP re-annotationNADP-dependent isocitrate dehydrogenase
Revised (this work)NADP-dependent isocitrate dehydrogenase. Pfam: IDH (PF03971.20).

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

Curated reference (UniProt)

UniProt O53611 SwissProt · reviewed · Evidence at protein level
UniProt nameIsocitrate dehydrogenase [NADP] 2
EC (curated) EC 1.1.1.42
Curated functionCatalyzes the oxidative decarboxylation of isocitrate to 2-oxoglutarate and carbon dioxide with the concomitant reduction of NADP(+). Cannot use NAD(+).

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category C Energy production and conversion
Preferred nameicd
eggNOG descriptionIsocitrate dehydrogenase
Orthologous groupCOG2838
EC number EC 1.1.1.42
KEGG orthology K00031
KEGG pathways map00020, map00480, map00720, map01100, map01110, map01120, map01130, map01200, map01210, map01230, map04146
KEGG modules M00009, M00010, M00173, M00740

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 0.302 · purifying
Polymorphic sites (≥ 0.1% of strains) 11 synonymous, 11 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
IDHPF03971.20 0.0e+007–740 Monomeric isocitrate dehydrogenase

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv2455c korA 2-oxoglutarate oxidoreductase subunit KorA 987 975 coexpression:668 database:900 textmining:516
Rv2454c korB 2-oxoglutarate oxidoreductase subunit KorB 946 944 coexpression:417 database:900
Rv1475c acn iron-regulated aconitate hydratase 965 919 database:900 textmining:591
Rv3339c icd1 isocitrate dehydrogenase 938 908 database:900
Rv1240 mdh malate dehydrogenase 934 870 coexpression:859 textmining:517
Rv0777 purB adenylosuccinate lyase PurB 839 839 database:800
Rv2476c gdh NAD-dependent glutamate dehydrogenase 827 812 database:800
Rv1731 gabD2 succinate-semialdehyde dehydrogenase 810 810 database:800
Rv0234c gabD1 succinate-semialdehyde dehydrogenase 810 810 database:800
Rv1595 nadB L-aspartate oxidase 809 809 database:800
Rv0337c aspC aspartate aminotransferase 806 807 database:800
Rv3858c gltD glutamate synthase small subunit 812 806 database:800
Rv1659 argH argininosuccinate lyase 815 804 database:800
Rv3859c gltB glutamate synthase large subunit 921 801 database:800 textmining:622
Rv2280 Rv2280, (MTCY339.30c), len: 459 aa. Probable dehydrogenase. Similar to D-lactate dehydrogenase (cytochrome) precursor e.g. G1061264 (587 aa) 745 738 coexpression:738

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: isocitrate dehydrogenase
  • MTBC0 PGAP product: NADP-dependent isocitrate dehydrogenase
  • Pfam (hmmscan --cut_ga): IDH PF03971.20 (E=0e+00)
  • (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_214580.1)
  • Domains: Pfam-A via hmmscan --cut_ga — IDH (PF03971.20)
  • 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 COG2838
  • Curated reference: UniProt O53611 (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)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000073|Rv0066c|icd2
MSAEQPTIIYTLTDEAPLLATYAFLPIVRAFAEPAGIKIEASDISVAARILAEFPDYLTEEQRVPDNLAELGRLTQLPDTNIIKLPNISASVPQLVAAIKELQDKGYAVPDYPADPKTDQEKAIKERYARCLGSAVNPVLRQGNSDRRAPKAVKEYARKHPHSMGEWSMASRTHVAHMRHGDFYAGEKSMTLDRARNVRMELLAKSGKTIVLKPEVPLDDGDVIDSMFMSKKALCDFYEEQMQDAFETGVMFSLHVKATMMKVSHPIVFGHAVRIFYKDAFAKHQELFDDLGVNVNNGLSDLYSKIESLPASQRDEIIEDLHRCHEHRPELAMVDSARGISNFHSPSDVIVDASMPAMIRAGGKMYGADGKLKDTKAVNPESTFSRIYQEIINFCKTNGQFDPTTMGTVPNVGLMAQQAEEYGSHDKTFEIPEDGVANIVDVATGEVLLTENVEAGDIWRMCIVKDAPIRDWVKLAVTRARISGMPVLFWLDPYRPHENELIKKVKTYLKDHDTEGLDIQIMSQVRSMRYTCERLVRGLDTIAATGNILRDYLTDLFPILELGTSAKMLSVVPLMAGGGMYETGAGGSAPKHVKQLVEENHLRWDSLGEFLALGAGFEDIGIKTGNERAKLLGKTLDAAIGKLLDNDKSPSRKTGELDNRGSQFYLAMYWAQELAAQTDDQQLAEHFASLADVLTKNEDVIVRELTEVQGEPVDIGGYYAPDSDMTTAVMRPSKTFNAALEAVQG