gabD1 Resolved · high auto-curated

H37Rv Rv0234c · MTBC0 - · 511 aa · 279605–281140 (-) · RefSeq NP_216247.2

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)succinate-semialdehyde dehydrogenase
MTBC0 PGAP re-annotation
Revised (this work)Succinate-semialdehyde dehydrogenase. Pfam: Aldedh (PF00171.28).

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 P9WNX9 SwissProt · reviewed · Evidence at protein level
UniProt nameSuccinate-semialdehyde dehydrogenase [NADP(+)] 1
EC (curated) EC 1.2.1.79
Curated functionCatalyzes the NADP(+)-dependent oxidation of succinate semialdehyde to succinate. It is believed to be the main source of succinate semialdehyde dehydrogenase activity in Mycobacterium. NAD(+) can substitute for NADP(+), but enzymatic activity is three times reduced.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category C Energy production and conversion
Preferred namegabD1
eggNOG descriptionCatalyzes the NADP( )-dependent oxidation of succinate semialdehyde to succinate. It is believed to be the main source of succinate semialdehyde dehydrogenase activity in Mycobacterium
Orthologous groupCOG1012
EC number EC 1.2.1.16, EC 1.2.1.20, EC 1.2.1.79
KEGG orthology K00135
KEGG pathways map00250, map00310, map00350, map00650, map00760, map01100, map01120
KEGG modules M00027
Gene Ontology (32) GO:0003674, GO:0003824, GO:0005575, GO:0005623, GO:0005886, GO:0006082, GO:0006091, GO:0006099, GO:0006101, GO:0008150, GO:0008152, GO:0009013 +20 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 1.027 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 2 synonymous, 6 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
AldedhPF00171.28 2.3e-14357–508 Aldehyde dehydrogenase family

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv2589 gabT 4-aminobutyrate aminotransferase 937 933 database:900
Rv3318 sdhA succinate dehydrogenase flavoprotein subunit 933 931 database:900
Rv0248c succinate dehydrogenase flavoprotein subunit 932 930 database:900
Rv1731 gabD2 succinate-semialdehyde dehydrogenase 925 925 database:900
Rv0247c succinate dehydrogenase iron-sulfur subunit 915 912 database:900
Rv3319 sdhB succinate dehydrogenase iron-sulphur protein subunit 915 912 database:900
Rv3316 sdhC succinate dehydrogenase cytochrome B-556 subunit 910 909 database:900
Rv3317 sdhD succinate dehydrogenase hydrophobic membrane anchor subunit 909 906 database:900
Rv1131 prpC methylcitrate synthase PrpC 896 889 database:800
Rv0896 gltA2 citrate synthase 1 894 889 database:800
Rv0889c citA citrate synthase 2 894 889 database:800
Rv2852c mqo malate:quinone oxidoreductase 851 843 database:800
Rv2455c korA 2-oxoglutarate oxidoreductase subunit KorA 869 830 database:800
Rv1240 mdh malate dehydrogenase 839 829 database:800
Rv1098c fum fumarate hydratase 837 828 database:800

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): succinate-semialdehyde dehydrogenase
  • Pfam (hmmscan --cut_ga): Aldedh PF00171.28 (E=2e-143)
  • (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_216247.2)
  • Domains: Pfam-A via hmmscan --cut_ga — Aldedh (PF00171.28)
  • 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 COG1012
  • Curated reference: UniProt P9WNX9 (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 — 73 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv0234c|gabD1
MRSVTCSATLVLPVIEPTPADRRPRHLLLGSAGHVSGRLDTGRFVQTHPAKDVSVPIATINPATGETVKTFTAATDDEVDAAIARAHRRFADYRQTSFAQRARWANATADLLEAEADQAAAMMTLEMGKTLAAAKAEALKCAKGFRYYAENAEALLADEPADAAKVGASAAYGRYQPLGVILAVMPWNFPLWQAVRFAAPALMAGNVGLLKHASNVPQCALYLADVIARGGFPDGCFQTLLVSSGAVEAILRDPRVAAATLTGSEPAGQSVGAIAGNEIKPTVLELGGSDPFIVMPSADLDAAVSTAVTGRVQNNGQSCIAAKRFIVHADIYDDFVDKFVARMAALRVGDPTDPDTDVGPLATEQGRNEVAKQVEDAAAAGAVIRCGGKRLDRPGWFYPPTVITDISKDMALYTEEVFGPVASVFRAANIDEAVEIANATTFGLGSNAWTRDETEQRRFIDDIVAGQVFINGMTVSYPELPFGGVKRSGYGRELSAHGIREFCNIKTVWIA