fba Resolved · high auto-curated

H37Rv Rv0363c · MTBC0 mtbc0_000383 · 344 aa · 444627–445661 (-) · RefSeq NP_214877.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)fructose-bisphosphate aldolase
MTBC0 PGAP re-annotationclass II fructose-bisphosphate aldolase
Revised (this work)Class II fructose-bisphosphate aldolase. Pfam: F_bP_aldolase (PF01116.27).

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

Curated reference (UniProt)

UniProt P9WQA3 SwissProt · reviewed · Evidence at protein level
UniProt nameFructose-bisphosphate aldolase
EC (curated) EC 4.1.2.13
Curated functionCatalyzes the aldol condensation of dihydroxyacetone phosphate (DHAP or glycerone-phosphate) with glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bisphosphate (FBP) in gluconeogenesis and the reverse reaction in glycolysis.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category G Carbohydrate transport and metabolism
Preferred namefba
eggNOG descriptionfructose-bisphosphate aldolase
Orthologous groupCOG0191
EC number EC 4.1.2.13
KEGG orthology K01624
KEGG pathways map00010, map00030, map00051, map00680, map00710, map01100, map01110, map01120, map01130, map01200, map01230
KEGG modules M00001, M00003, M00165, M00167, M00344, M00345
Gene Ontology (145) GO:0003674, GO:0003824, GO:0004332, GO:0005488, GO:0005515, GO:0005575, GO:0005576, GO:0005618, GO:0005622, GO:0005623, GO:0005737, GO:0005829 +133 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 0.515 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 5 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
F_bP_aldolasePF01116.27 4.8e-819–340 Fructose-bisphosphate aldolase class-II

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv1436 gap glyceraldehyde 3-phosphate dehydrogenase 992 982 coexpression:793 database:900 textmining:573
Rv1438 tpi triosephosphate isomerase 995 977 coexpression:763 database:900 textmining:831
Rv1023 eno enolase 986 964 coexpression:802 database:800 textmining:636
Rv0946c pgi glucose-6-phosphate isomerase 978 949 coexpression:735 database:800 textmining:596
Rv3010c pfkA 6-phosphofructokinase 977 948 database:900 textmining:595
Rv1449c tkt transketolase 973 948 coexpression:461 database:900 textmining:511
Rv1448c tal transaldolase 981 945 coexpression:431 database:900 textmining:682
Rv2029c pfkB 6-phosphofructokinase PfkB 967 939 database:900 textmining:481
Rv0489 gpm1 2,3-bisphosphoglycerate-dependent phosphoglycerate mutase 953 922 coexpression:624 database:800 textmining:429
Rv1099c glpX fructose 1,6-bisphosphatase 947 915 database:900 textmining:414
Rv0727c fucA L-fuculose phosphate aldolase FucA 924 909 database:900
Rv1617 pykA pyruvate kinase 943 906 coexpression:440 database:800 textmining:420
Rv0478 deoC 2-deoxyribose-5-phosphate aldolase 915 902 database:900
Rv1437 pgk phosphoglycerate kinase 958 884 coexpression:827 textmining:653
Rv2241 aceE pyruvate dehydrogenase E1 component 877 826 database:800

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: fructose-bisphosphate aldolase
  • MTBC0 PGAP product: class II fructose-bisphosphate aldolase
  • Pfam (hmmscan --cut_ga): F_bP_aldolase PF01116.27 (E=5e-81)
  • (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_214877.1)
  • Domains: Pfam-A via hmmscan --cut_ga — F_bP_aldolase (PF01116.27)
  • 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 COG0191
  • Curated reference: UniProt P9WQA3 (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 — 133 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000383|Rv0363c|fba
MPIATPEVYAEMLGQAKQNSYAFPAINCTSSETVNAAIKGFADAGSDGIIQFSTGGAEFGSGLGVKDMVTGAVALAEFTHVIAAKYPVNVALHTDHCPKDKLDSYVRPLLAISAQRVSKGGNPLFQSHMWDGSAVPIDENLAIAQELLKAAAAAKIILEIEIGVVGGEEDGVANEINEKLYTSPEDFEKTIEALGAGEHGKYLLAATFGNVHGVYKPGNVKLRPDILAQGQQVAAAKLGLPADAKPFDFVFHGGSGSLKSEIEEALRYGVVKMNVDTDTQYAFTRPIAGHMFTNYDGVLKVDGEVGVKKVYDPRSYLKKAEASMSQRVVQACNDLHCAGKSLTH