coaE Resolved · high auto-curated

H37Rv Rv1631 · MTBC0 mtbc0_001739 · 407 aa · 1846977–1848200 (+) · RefSeq NP_216147.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)dephospho-CoA kinase CoaE
MTBC0 PGAP re-annotationdephospho-CoA kinase
Revised (this work)Dephospho-CoA kinase. Pfam: CoaE (PF01121.27), GrpB (PF04229.21).

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

Curated reference (UniProt)

UniProt P9WPA3 SwissProt · reviewed · Evidence at protein level
UniProt nameDephospho-CoA kinase
EC (curated) EC 2.7.1.24
Curated functionCatalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A. Can also use dATP, with lower efficiency, but cannot use GTP, dGTP or CTP.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category F Nucleotide transport and metabolism
Preferred namecoaE
eggNOG descriptionCatalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A
Orthologous groupCOG0237
EC number EC 2.7.1.24
KEGG orthology K00859
KEGG pathways map00770, map01100
KEGG modules M00120
Gene Ontology (96) GO:0000166, GO:0001882, GO:0001884, GO:0002135, GO:0003674, GO:0003824, GO:0004140, GO:0005488, GO:0005575, GO:0005622, GO:0005623, GO:0005737 +84 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 0.278 · purifying
Polymorphic sites (≥ 0.1% of strains) 5 synonymous, 4 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
CoaEPF01121.27 1.4e-624–178 Dephospho-CoA kinase
GrpBPF04229.21 2.6e-36211–395 GrpB protein

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

Closest characterised functional partner: rpsA (30S ribosomal protein S1), high confidence from genomic context alone (score 864 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2965c kdtB phosphopantetheine adenylyltransferase 994 911 database:900 textmining:938
Rv2523c acpS holo-ACP synthase 915 907 database:900
Rv1630 rpsA 30S ribosomal protein S1 877 864 ctx neighborhood:844
Rv1629 polA DNA polymerase I 922 856 ctx neighborhood:726 coexpression:405 textmining:488
Rv1870c hyp hypothetical protein 811 812 coexpression:801
Rv2902c rnhB ribonuclease HII 786 787 coexpression:772
Rv3433c nnr bifunctional ADP-dependent (S)-NAD(P)H-hydrate dehydratase/NAD(P)H-hydrate epimerase 663 663 ctx neighborhood:544
Rv0176 Mce associated transmembrane protein 659 659 coexpression:651
Rv2924c fpg formamidopyrimidine-DNA glycosylase 645 611 coexpression:472
Rv3396c guaA GMP synthase 623 605 ctx neighborhood:544
Rv2551c hyp hypothetical protein 613 598 coexpression:459
Rv1650 pheT phenylalanine--tRNA ligase subunit beta 691 567 ctx neighborhood:544
Rv2946c pks1 polyketide synthase 621 563 ctx neighborhood:544
Rv2438c nadE glutamine-dependent NAD(+) synthetase 759 554 ctx neighborhood:544 textmining:482
Rv2230c GTP cyclohydrolase 547 548 ctx neighborhood:544

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: dephospho-CoA kinase CoaE
  • MTBC0 PGAP product: dephospho-CoA kinase
  • Pfam (hmmscan --cut_ga): CoaE PF01121.27 (E=1e-62), GrpB PF04229.21 (E=3e-36)
  • (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_216147.1)
  • Domains: Pfam-A via hmmscan --cut_ga — CoaE (PF01121.27), GrpB (PF04229.21)
  • 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 COG0237
  • Curated reference: UniProt P9WPA3 (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 — 95 functional partner(s); context anchor rpsA
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001739|Rv1631|coaE
MLRIGLTGGIGAGKSLLSTTFSQCGGIVVDGDVLAREVVQPGTEGLASLVDAFGRDILLADGALDRQALAAKAFRDDESRGVLNGIVHPLVARRRSEIIAAVSGDAVVVEDIPLLVESGMAPLFPLVVVVHADVELRVRRLVEQRGMAEADARARIAAQASDQQRRAVADVWLDNSGSPEDLVRRARDVWNTRVQPFAHNLAQRQIARAPARLVPADPSWPDQARRIVNRLKIACGHKALRVDHIGSTAVSGFPDFLAKDVIDIQVTVESLDVADELAEPLLAAGYPRLEHITQDTEKTDARSTVGRYDHTDSAALWHKRVHASADPGRPTNVHLRVHGWPNQQFALLFVDWLAANPGAREDYLTVKCDADRRADGELARYVTAKEPWFLDAYQRAWEWADAVHWRP