gpm1 Resolved · high auto-curated

H37Rv Rv0489 · MTBC0 - · 249 aa · 578426–579175 (+) · RefSeq YP_177731.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)2,3-bisphosphoglycerate-dependent phosphoglycerate mutase
MTBC0 PGAP re-annotation
Revised (this work)2,3-bisphosphoglycerate-dependent phosphoglycerate mutase. Pfam: His_Phos_1 (PF00300.28).

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 P9WIC9 SwissProt · reviewed · Evidence at protein level
UniProt name2,3-bisphosphoglycerate-dependent phosphoglycerate mutase
EC (curated) EC 5.4.2.11
Curated functionCatalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category G Carbohydrate transport and metabolism
Preferred namegpmA
eggNOG descriptionCatalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate
Orthologous groupCOG0588
EC number EC 5.4.2.11
KEGG orthology K01834
KEGG pathways map00010, map00260, map00680, map01100, map01110, map01120, map01130, map01200, map01230, map04922, map05230
KEGG modules M00001, M00002, M00003
Gene Ontology (173) GO:0003674, GO:0003824, GO:0004619, GO:0005488, GO:0005515, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0005886, GO:0005975 +161 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 0.0 · strong purifying
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 0 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
His_Phos_1PF00300.28 1.5e-307–206 Histidine phosphatase superfamily (branch 1)

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

Closest characterised functional partner: senX3 (two component sensor histidine kinase SenX3), high confidence from genomic context alone (score 747 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1437 pgk phosphoglycerate kinase 990 975 coexpression:727 database:900 textmining:648
Rv1023 eno enolase 987 971 coexpression:665 database:900 textmining:587
Rv0728c serA2 D-3-phosphoglycerate dehydrogenase SerA 944 939 database:900
Rv0363c fba fructose-bisphosphate aldolase 953 922 coexpression:624 database:800 textmining:429
Rv0946c pgi glucose-6-phosphate isomerase 959 920 coexpression:614 database:800 textmining:511
Rv2996c serA1 D-3-phosphoglycerate dehydrogenase 924 916 database:900
Rv2205c hyp hypothetical protein 905 900 database:900
Rv1448c tal transaldolase 885 839 database:800
Rv1449c tkt transketolase 870 838 database:800
Rv1121 zwf1 glucose-6-phosphate 1-dehydrogenase 851 832 database:800
Rv1447c zwf2 glucose-6-phosphate 1-dehydrogenase 850 831 database:800
Rv1438 tpi triosephosphate isomerase 948 824 coexpression:787 textmining:720
Rv0478 deoC 2-deoxyribose-5-phosphate aldolase 807 802 database:800
Rv0490 senX3 two component sensor histidine kinase SenX3 773 747 ctx neighborhood:743
Rv0491 regX3 two component sensory transduction protein RegX 696 673 ctx neighborhood:660

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): 2,3-bisphosphoglycerate-dependent phosphoglycerate mutase
  • Pfam (hmmscan --cut_ga): His_Phos_1 PF00300.28 (E=1e-30)
  • (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 YP_177731.1)
  • Domains: Pfam-A via hmmscan --cut_ga — His_Phos_1 (PF00300.28)
  • 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 COG0588
  • Curated reference: UniProt P9WIC9 (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 — 78 functional partner(s); context anchor senX3
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv0489|gpm1
MANTGSLVLLRHGESDWNALNLFTGWVDVGLTDKGQAEAVRSGELIAEHDLLPDVLYTSLLRRAITTAHLALDSADRLWIPVRRSWRLNERHYGALQGLDKAETKARYGEEQFMAWRRSYDTPPPPIERGSQFSQDADPRYADIGGGPLTECLADVVARFLPYFTDVIVGDLRVGKTVLIVAHGNSLRALVKHLDQMSDDEIVGLNIPTGIPLRYDLDSAMRPLVRGGTYLDPEAAAAGAAAVAGQGRG