fbiA Resolved · high auto-curated

H37Rv Rv3261 · MTBC0 mtbc0_003469 · 331 aa · 3662686–3663681 (+) · RefSeq NP_217778.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)2-phospho-L-lactate transferase
MTBC0 PGAP re-annotation2-phospho-L-lactate transferase
Revised (this work)2-phospho-L-lactate transferase. Pfam: CofD (PF01933.24).

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

Curated reference (UniProt)

UniProt P9WP81 SwissProt · reviewed · Evidence at protein level
UniProt namePhosphoenolpyruvate transferase
EC (curated) EC 2.7.8.28
Curated functionCatalyzes the transfer of the phosphoenolpyruvate moiety from enoylpyruvoyl-2-diphospho-5'-guanosine (EPPG) to 7,8-didemethyl-8-hydroxy-5-deazariboflavin (FO) with the formation of dehydro coenzyme F420-0 and GMP.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category H Coenzyme transport and metabolism
Preferred namecofD
eggNOG descriptionCatalyzes the transfer of the 2-phospholactate moiety from lactyl (2) diphospho-(5')guanosine (LPPG) to 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) with the formation of the L- lactyl phosphodiester of 7,8-didemethyl-8-hydroxy-5- deazariboflavin (F420-0) and GMP
Orthologous groupCOG0391
EC number EC 2.7.8.28
KEGG orthology K11212
KEGG pathways map00680, map01120
KEGG modules M00378
Gene Ontology (16) GO:0003674, GO:0003824, GO:0006732, GO:0008150, GO:0008152, GO:0009058, GO:0009108, GO:0009987, GO:0016740, GO:0016772, GO:0016773, GO:0043743 +4 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 0.685 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 2 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
CofDPF01933.24 2.6e-603–294 2-phospho-L-lactate transferase CofD

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

Closest characterised functional partner: fbiB (coenzyme F420:L-glutamate ligase), high confidence from genomic context alone (score 999 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv3262 fbiB coenzyme F420:L-glutamate ligase 999 999 ctx neighborhood:882 cooccurence:773 coexpression:797 database:900 textmining:908
Rv2983 cofC 2-phospho-L-lactate guanylyltransferase 998 979 ctx cooccurence:773 database:900 textmining:948
Rv1173 fbiC FO synthase 997 975 ctx cooccurence:727 database:900 textmining:893
Rv3547 ddn deazaflavin-dependent nitroreductase 976 768 ctx cooccurence:762 textmining:903
Rv0132c fgd2 F420-dependent glucose-6-phosphate dehydrogenase 878 758 ctx cooccurence:750 textmining:520
Rv3178 nitroreductase 869 753 ctx cooccurence:746 textmining:493
Rv1558 hyp hypothetical protein 835 751 ctx cooccurence:747
Rv3520c coenzyme F420-dependent oxidoreductase 763 750 ctx cooccurence:741
Rv1261c hyp hypothetical protein 755 749 ctx cooccurence:747
Rv0407 fgd1 F420-dependent glucose-6-phosphate dehydrogenase 990 747 ctx cooccurence:728 textmining:965
Rv2951c phthiodiolone/phenolphthiodiolone dimycocerosates ketoreductase 760 747 ctx cooccurence:737
Rv3093c oxidoreductase 760 747 ctx cooccurence:739
Rv0044c oxidoreductase 742 729 ctx cooccurence:718
Rv1855c oxidoreductase 742 728 ctx cooccurence:716
Rv3263 DNA methylase 725 725 ctx neighborhood:718

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: 2-phospho-L-lactate transferase
  • MTBC0 PGAP product: 2-phospho-L-lactate transferase
  • Pfam (hmmscan --cut_ga): CofD PF01933.24 (E=3e-60)
  • (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_217778.1)
  • Domains: Pfam-A via hmmscan --cut_ga — CofD (PF01933.24)
  • 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 COG0391
  • Curated reference: UniProt P9WP81 (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 — 56 functional partner(s); context anchor fbiB
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003469|Rv3261|fbiA
MKVTVLAGGVGGARFLLGVQQLLGLGQFAANSAHSDADHQLSAVVNVGDDAWIHGLRVCPDLDTCMYTLGGGVDPQRGWGQRDETWHAMQELVRYGVQPDWFELGDRDLATHLVRTQMLQAGYPLSQITEALCDRWQPGARLLPATDDRCETHVVITDPVDESRKAIHFQEWWVRYRAQVPTHSFAFVGAEKSSAATEAIAALADADIIMLAPSNPVVSIGAILAVPGIRAALREATAPIVGYSPIIGEKPLRGMADTCLSVIGVDSTAAAVGRHYGARCATGILDCWLVHDGDHAEIDGVTVRSVPLLMTDPNATAEMVRAGCDLAGVVA