ino1 Resolved · high auto-curated

H37Rv Rv0046c · MTBC0 mtbc0_000051 · 367 aa · 50120–51223 (-) · RefSeq NP_214560.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)inositol-3-phosphate synthase
MTBC0 PGAP re-annotationinositol-3-phosphate synthase
Revised (this work)Inositol-3-phosphate synthase. Pfam: Inos-1-P_synth (PF01658.23).

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

Curated reference (UniProt)

UniProt P9WKI1 SwissProt · reviewed · Evidence at protein level
UniProt nameInositol-3-phosphate synthase
EC (curated) EC 5.5.1.4
Curated functionKey enzyme in myo-inositol biosynthesis pathway that catalyzes the conversion of glucose 6-phosphate to 1D-myo-inositol 3-phosphate in a NAD-dependent manner.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category I Lipid transport and metabolism
Preferred nameino1
eggNOG descriptionsynthase
Orthologous groupCOG1260
EC number EC 5.5.1.4
KEGG orthology K01858
KEGG pathways map00521, map00562, map01100, map01130
Gene Ontology (42) GO:0003674, GO:0003824, GO:0004512, GO:0005488, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0006790, GO:0008150, GO:0008152 +30 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 0.733 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 7 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
Inos-1-P_synthPF01658.23 2.3e-35203–311 Myo-inositol-1-phosphate synthase

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

Closest characterised functional partner: pgsA1 (CDP-diacylglycerol--inositol 3-phosphatidyltransferase), high confidence from genomic context alone (score 861 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1604 impA inositol-monophosphatase ImpA 983 908 database:900 textmining:827
Rv2701c suhB inositol-1-monophosphatase SuhB 959 908 database:900 textmining:582
Rv0650 sugar kinase 923 901 database:900
Rv3068c pgmA phosphoglucomutase PgmA 946 900 database:900 textmining:489
Rv2612c pgsA1 CDP-diacylglycerol--inositol 3-phosphatidyltransferase 896 861 ctx cooccurence:712 database:500
Rv0047c hyp hypothetical protein 959 841 ctx neighborhood:802 textmining:755
Rv0044c oxidoreductase 781 777 ctx neighborhood:776
Rv0045c hydrolase 709 710 ctx neighborhood:671
Rv0043c HTH-type transcriptional regulator 696 697 ctx neighborhood:695
Rv0486 mshA D-inositol 3-phosphate glycosyltransferase 690 672 database:500
Rv0042c transcriptional regulator 521 522 ctx neighborhood:520
Rv0048c membrane protein 511 511 ctx neighborhood:508
Rv0049 hyp hypothetical protein 449 450 ctx neighborhood:445
Rv2610c pimA alpha-(1-2)-phosphatidylinositol mannosyltransferase 483 299
Rv3774 echA21 enoyl-CoA hydratase EchA21 576 149 textmining:524

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: inositol-3-phosphate synthase
  • MTBC0 PGAP product: inositol-3-phosphate synthase
  • Pfam (hmmscan --cut_ga): Inos-1-P_synth PF01658.23 (E=2e-35)
  • (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_214560.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Inos-1-P_synth (PF01658.23)
  • 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 COG1260
  • Curated reference: UniProt P9WKI1 (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 — 30 functional partner(s); context anchor pgsA1
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000051|Rv0046c|ino1
MSEHQSLPAPEASTEVRVAIVGVGNCASSLVQGVEYYYNADDTSTVPGLMHVRFGPYHVRDVKFVAAFDVDAKKVGFDLSDAIFASENNTIKIADVAPTNVIVQRGPTLDGIGKYYADTIELSDAEPVDVVQALKEAKVDVLVSYLPVGSEEADKFYAQCAIDAGVAFVNALPVFIASDPVWAKKFTDAGVPIVGDDIKSQVGATITHRVLAKLFEDRGVQLDRTMQLNVGGNMDFLNMLERERLESKKISKTQAVTSNLKREFKTKDVHIGPSDHVGWLDDRKWAYVRLEGRAFGDVPLNLEYKLEVWDSPNSAGVIIDAVRAAKIAKDRGIGGPVIPASAYLMKSPPEQLPDDIARAQLEEFIIG