purT Resolved · high auto-curated

H37Rv Rv0389 · MTBC0 mtbc0_000408 · 419 aa · 471699–472958 (+) · RefSeq NP_214903.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)phosphoribosylglycinamide formyltransferase PurT
MTBC0 PGAP re-annotationphosphoribosylglycinamide formyltransferase 2
Revised (this work)Phosphoribosylglycinamide formyltransferase 2. Pfam: ATP-grasp (PF02222.28).

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

Curated reference (UniProt)

UniProt P95197 TrEMBL · unreviewed · Evidence at protein level
UniProt namePhosphoribosylglycinamide formyltransferase 2

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category F Nucleotide transport and metabolism
Preferred namepurT
eggNOG descriptionInvolved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate
Orthologous groupCOG0027
EC number EC 2.1.2.2
KEGG orthology K08289
KEGG pathways map00230, map00670, map01100, map01110, map01130
KEGG modules M00048
Gene Ontology (22) GO:0003674, GO:0003824, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0006793, GO:0006796, GO:0008150, GO:0008152, GO:0008776 +10 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 0.511 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 5 synonymous, 6 missense, 1 nonsense, 1 frameshift
Disruption 2 distinct premature-stop/frameshift site(s); most common in 0.48% of strains (690) · 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
ATP-graspPF02222.28 1.7e-23137–325 ATP-grasp domain

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv0788 purQ phosphoribosylformylglycinamidine synthase 980 974 coexpression:731 database:900
Rv0803 purL phosphoribosylformylglycinamidine synthase 2 980 974 coexpression:731 database:900
Rv0957 purH bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/inosinemonophosphate cyclohydrolase 979 973 coexpression:742 database:900
Rv0772 purD phosphoribosylamine--glycine ligase 973 966 coexpression:646 database:900
Rv0956 purN phosphoribosylglycinamide formyltransferase PurN 968 959 coexpression:610 database:900
Rv1093 glyA1 serine hydroxymethyltransferase 916 914 database:900
Rv0070c glyA2 serine hydroxymethyltransferase 916 913 database:900
Rv2211c gcvT aminomethyltransferase 913 913 database:900
Rv0787A purS hyp hypothetical protein 929 908 database:900
Rv2964 purU formyltetrahydrofolate deformylase 920 904 database:900
Rv0992c 5-formyltetrahydrofolate cyclo-ligase 908 904 database:900
Rv1406 fmt methionyl-tRNA formyltransferase 900 901 database:900
Rv2124c metH methionine synthase 900 901 database:900
Rv3356c folD bifunctional methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase 906 900 database:900
Rv2763c dfrA dihydrofolate reductase 900 900 database:900

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: phosphoribosylglycinamide formyltransferase PurT
  • MTBC0 PGAP product: phosphoribosylglycinamide formyltransferase 2
  • Pfam (hmmscan --cut_ga): ATP-grasp PF02222.28 (E=2e-23)
  • (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_214903.1)
  • Domains: Pfam-A via hmmscan --cut_ga — ATP-grasp (PF02222.28)
  • 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 COG0027
  • Curated reference: UniProt P95197 (TrEMBL, unreviewed; 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 — 39 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000408|Rv0389|purT
MIDGWTEGQHEPTVRHERPAAPQDVRRVMLLGSAEPSRELAIALQGLGAEVIAVDGYVGAPAHRIADQSVVVTMTDAEELTAVIRRLQPDFLVTVTAAVSVDALDAVEQADGECTELVPNARAVRCTADREGLRRLAADQLGLPTAPFWFVGSLGELQAVAVHAGFPLLVSPVAGVAGQGSSVVAGPNEVEPAWQRAAGHQVQPQTGGVSPRVCAESVVEIEFLVTMIVVCSQGPNGPLIEFCAPIGHRDADAGELESWQPQKLSTAALDAAKSIAARIVKALGGRGVFGVELMINGDEVYFADVTVCPAGSAWVTVRSQRLSVFELQARAILGLAVDTLMISPGAARVINPDHTAGRAAVGAAPPADALTGALGVPESDVVIFGRGLGVALATAPEVAIARERAREVASRLNVPDSRE