snoP Family assigned · medium auto-curated

H37Rv Rv2604c · MTBC0 mtbc0_002772 · 198 aa · 2955246–2955842 (-) · RefSeq NP_217120.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)glutamine amidotransferase SnoP
MTBC0 PGAP re-annotationpyridoxal 5'-phosphate synthase glutaminase subunit PdxT
Revised (this work)Pyridoxal 5'-phosphate synthase glutaminase subunit PdxT. Pfam: SNO (PF01174.26), GATase_3 (PF07685.21).

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

Curated reference (UniProt)

UniProt P9WII7 SwissProt · reviewed · Evidence at protein level
UniProt namePyridoxal 5'-phosphate synthase subunit PdxT
EC (curated) EC 3.5.1.2, EC 4.3.3.6
Curated functionCatalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category H Coenzyme transport and metabolism
Preferred namepdxT
eggNOG descriptionCatalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS
Orthologous groupCOG0311
EC number EC 4.3.3.6
KEGG orthology K08681
KEGG pathways map00750
Gene Ontology (73) GO:0003674, GO:0003824, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0005829, GO:0006081, GO:0006725, GO:0006732, GO:0006766, GO:0006767 +61 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 0.559 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 2 synonymous, 3 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
SNOPF01174.26 8.9e-598–194 SNO glutamine amidotransferase family
GATase_3PF07685.21 1.1e-0719–96 CobB/CobQ-like glutamine amidotransferase domain

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

Closest characterised functional partner: snzP (pyridoxine biosynthesis protein), high confidence from genomic context alone (score 1000 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2606c snzP pyridoxine biosynthesis protein 999 1000 ctx neighborhood:822 cooccurence:774 coexpression:855 experimental:928 database:900 textmining:948
Rv2607 pdxH pyridoxine/pyridoxamine 5'-phosphate oxidase 994 947 ctx neighborhood:496 database:900 textmining:898
Rv2605c tesB2 acyl-CoA thioesterase II 984 884 ctx neighborhood:882 textmining:870
Rv1448c tal transaldolase 816 817 database:800
Rv1449c tkt transketolase 801 801 database:800
Rv1017c prsA ribose-phosphate pyrophosphokinase 801 801 database:800
Rv2436 rbsK ribokinase RbsK 819 800 database:800
Rv3068c pgmA phosphoglucomutase PgmA 800 800 database:800
Rv2465c rpiB ribose-5-phosphate isomerase B 800 800 database:800
Rv2603c transcriptional regulator 854 760 ctx neighborhood:757 textmining:418
Rv2613c AP-4-A phosphorylase 550 551 ctx neighborhood:544
Rv2614c thrS threonine--tRNA ligase 547 548 ctx neighborhood:544
Rv3581c ispF 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase 426 427 coexpression:420
Rv3396c guaA GMP synthase 544 131 textmining:497
Rv1850 ureC urease subunit alpha 517 46 textmining:515

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: glutamine amidotransferase SnoP
  • MTBC0 PGAP product: pyridoxal 5'-phosphate synthase glutaminase subunit PdxT
  • Pfam (hmmscan --cut_ga): SNO PF01174.26 (E=9e-59), GATase_3 PF07685.21 (E=1e-07)
  • (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_217120.1)
  • Domains: Pfam-A via hmmscan --cut_ga — SNO (PF01174.26), GATase_3 (PF07685.21)
  • 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 COG0311
  • Curated reference: UniProt P9WII7 (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 — 20 functional partner(s); context anchor snzP
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_002772|Rv2604c|snoP
MSVPRVGVLALQGDTREHLAALRECGAEPMTVRRRDELDAVDALVIPGGESTTMSHLLLDLDLLGPLRARLADGLPAYGSCAGMILLASEILDAGAAGRQALPLRAMNMTVRRNAFGSQVDSFEGDIEFAGLDDPVRAVFIRAPWVERVGDGVQVLARAAGHIVAVRQGAVLATAFHPEMTGDRRIHQLFVDIVTSAA