glpK Resolved · high auto-curated

H37Rv Rv3696c · MTBC0 mtbc0_003917 · 517 aa · 4162150–4163703 (-) · RefSeq NP_218213.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)glycerol kinase
MTBC0 PGAP re-annotationglycerol kinase GlpK
Revised (this work)Glycerol kinase GlpK. Pfam: FGGY_N (PF00370.28), FGGY_C (PF02782.23).

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

Curated reference (UniProt)

UniProt P9WPK1 SwissProt · reviewed · Evidence at protein level
UniProt nameGlycerol kinase
EC (curated) EC 2.7.1.30
Curated functionKey enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn-glycerol 3-phosphate.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category F Nucleotide transport and metabolism
Preferred nameglpK
eggNOG descriptionKey enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate
Orthologous groupCOG0554
EC number EC 2.7.1.30
KEGG orthology K00864
KEGG pathways map00561, map01100, map03320, map04626
Gene Ontology (24) GO:0003674, GO:0003824, GO:0004370, GO:0005975, GO:0006066, GO:0006071, GO:0006793, GO:0006796, GO:0008150, GO:0008152, GO:0009987, GO:0016301 +12 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) pseudogene candidate

pN/pS 0.683 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 4 synonymous, 8 missense, 0 nonsense, 1 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 2.14% of strains (3102) · clonal

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
FGGY_NPF00370.28 3.2e-6817–268 FGGY family of carbohydrate kinases, N-terminal domain
FGGY_CPF02782.23 1.7e-49278–467 FGGY family of carbohydrate kinases, C-terminal domain

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

Closest characterised functional partner: glpD2 (glycerol-3-phosphate dehydrogenase), high confidence from genomic context alone (score 994 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv3302c glpD2 glycerol-3-phosphate dehydrogenase 998 994 ctx fusion:796 cooccurence:741 coexpression:726 database:500 textmining:691
Rv2115c mpa proteasome-associated ATPase 990 989 experimental:916 database:844
Rv1334 mec [CysO 988 986 experimental:908 database:844
Rv2249c glpD1 glycerol-3-phosphate dehydrogenase 991 984 ctx fusion:516 cooccurence:744 coexpression:725 database:500 textmining:469
Rv2110c prcB proteasome subunit beta 936 929 experimental:791 database:662
Rv2109c prcA proteasome subunit alpha 936 928 experimental:791 database:662
Rv3045 adhC NADP-dependent alcohol dehydrogenase 916 911 database:900
Rv1692 phosphatase 913 905 database:900
Rv2482c plsB2 glycerol-3-phosphate acyltransferase 922 900 database:900
Rv1551 plsB1 acyltransferase PlsB 913 900 database:900
Rv1043c hyp hypothetical protein 769 754 experimental:402 database:589
Rv0125 pepA serine protease PepA 767 753 experimental:402 database:589
Rv0983 pepD serine protease PepD 767 753 experimental:402 database:589
Rv3671c marP serine protease 767 753 experimental:402 database:589
Rv1223 htrA serine protease HtrA 766 752 experimental:402 database:589

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: glycerol kinase
  • MTBC0 PGAP product: glycerol kinase GlpK
  • Pfam (hmmscan --cut_ga): FGGY_N PF00370.28 (E=3e-68), FGGY_C PF02782.23 (E=2e-49)
  • (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_218213.1)
  • Domains: Pfam-A via hmmscan --cut_ga — FGGY_N (PF00370.28), FGGY_C (PF02782.23)
  • 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 COG0554
  • Curated reference: UniProt P9WPK1 (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 — 134 functional partner(s); context anchor glpD2
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003917|Rv3696c|glpK
MSDAILGEQLAESSDFIAAIDQGTTSTRCMIFDHHGAEVARHQLEHEQILPRAGWVEHNPVEIWERTASVLISVLNATNLSPKDIAALGITNQRETTLVWNRHTGRPYYNAIVWQDTRTDRIASALDRDGRGNLIRRKAGLPPATYFSGGKLQWILENVDGVRAAAENGDALFGTPDTWVLWNLTGGPRGGVHVTDVTNASRTMLMDLETLDWDDELLSLFSIPRAMLPEIASSAPSEPYGVTLATGPVGGEVPITGVLGDQHAAMVGQVCLAPGEAKNTYGTGNFLLLNTGETIVRSNNGLLTTVCYQFGNAKPVYALEGSIAVTGSAVQWLRDQLGIISGAAQSEALARQVPDNGGMYFVPAFSGLFAPYWRSDARGAIVGLSRFNTNAHLARATLEAICYQSRDVVDAMEADSGVRLQVLKVDGGITGNDLCMQIQADVLGVDVVRPVVAETTALGAAYAAGLAVGFWAAPSDLRANWREDKRWTPTWDDDERAAGYAGWRKAVQRTLDWVDVS