Rv1301 Resolved · high auto-curated

H37Rv Rv1301 · MTBC0 mtbc0_001393 · 217 aa · 1466597–1467250 (+) · RefSeq NP_215817.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)threonylcarbamoyl-AMP synthase
MTBC0 PGAP re-annotationL-threonylcarbamoyladenylate synthase
Revised (this work)L-threonylcarbamoyladenylate synthase. Pfam: Sua5_yciO_yrdC (PF01300.25).

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

Curated reference (UniProt)

UniProt P9WGC9 SwissProt · reviewed · Evidence at protein level
UniProt namePutative threonylcarbamoyl-AMP synthase
EC (curated) EC 2.7.7.87
Curated functionRequired for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Catalyzes the conversion of L-threonine, HCO(3)(-)/CO(2) and ATP to give threonylcarbamoyl-AMP (TC-AMP) as the acyladenylate intermediate, with the release of diphosphate.

UniProt still lists this protein as Putative threonylcarbamoyl-AMP synthase; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category J Translation, ribosomal structure and biogenesis
Preferred nameywlC
eggNOG descriptionBelongs to the SUA5 family
Orthologous groupCOG0009
EC number EC 2.7.7.87
KEGG orthology K07566
Gene Ontology (47) GO:0000049, GO:0002949, GO:0003674, GO:0003676, GO:0003723, GO:0003824, GO:0005488, GO:0005575, GO:0005622, GO:0005623, GO:0005737, GO:0006139 +35 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 0.361 · purifying
Polymorphic sites (≥ 0.1% of strains) 2 synonymous, 2 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
Sua5_yciO_yrdCPF01300.25 8.3e-4823–197 Telomere recombination

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

Closest characterised functional partner: hemK (release factor glutamine methyltransferase), high confidence from genomic context alone (score 980 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1300 hemK release factor glutamine methyltransferase 982 980 ctx neighborhood:863 fusion:758 coexpression:440
Rv1299 prfA peptide chain release factor PrfA 874 867 ctx neighborhood:863
Rv1302 rfe decaprenyl-phosphate N-acetylglucosaminephosphotransferase 816 788 ctx neighborhood:782
Rv1298 rpmE 50S ribosomal protein L31 785 773 ctx neighborhood:767
Rv1297 rho transcription termination factor Rho 719 707 ctx neighborhood:502 coexpression:436
Rv1304 atpB ATP synthase subunit A 713 679 ctx neighborhood:676
Rv1303 hyp hypothetical protein 678 678 ctx neighborhood:676
Rv1305 atpE ATP synthase subunit C 690 673 ctx neighborhood:655
Rv1307 atpH ATP synthase subunit b/delta 697 652 ctx neighborhood:644
Rv1010 ksgA rRNA small subunit methyltransferase A 599 584 coexpression:413
Rv1311 atpC ATP synthase subunit epsilon 575 552 ctx neighborhood:531
Rv3422c tsaE tRNA threonylcarbamoyladenosine biosynthesis protein 650 543 database:500
Rv3859c gltB glutamate synthase large subunit 517 518 ctx neighborhood:511
Rv1278 hyp hypothetical protein 517 518 coexpression:454
Rv1988 erm(37) 23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(37) 518 500

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: threonylcarbamoyl-AMP synthase
  • MTBC0 PGAP product: L-threonylcarbamoyladenylate synthase
  • Pfam (hmmscan --cut_ga): Sua5_yciO_yrdC PF01300.25 (E=8e-48)
  • (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_215817.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Sua5_yciO_yrdC (PF01300.25)
  • 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 COG0009
  • Curated reference: UniProt P9WGC9 (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 — 42 functional partner(s); context anchor hemK
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001393|Rv1301|
MTETFDCADPEQRSRGIVSAVGAIKAGQLVVMPTDTVYGIGADAFDSSAVAALLSAKGRGRDMPVGVLVGSWHTIEGLVYSMPDGARELIRAFWPGALSLVVVQAPSLQWDLGDAHGTVMLRMPLHPVAIELLREVGPMAVSSANISGHPPPVDAEQARSQLGDHVAVYLDAGPSEQQAGSTIVDLTGATPRVLRQGPVSTERIAEVLGVDAASLFG