Rv1885c Resolved · high auto-curated

H37Rv Rv1885c · MTBC0 mtbc0_001999 · 199 aa · 2152327–2152926 (-) · RefSeq NP_216401.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)chorismate mutase
MTBC0 PGAP re-annotationchorismate mutase
Revised (this work)Chorismate mutase. Pfam: CM_2 (PF01817.27).

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

Curated reference (UniProt)

UniProt P9WIB9 SwissProt · reviewed · Evidence at protein level
UniProt nameSecreted chorismate mutase
EC (curated) EC 5.4.99.5
Curated functionCatalyzes the Claisen rearrangement of chorismate to prephenate. May play some role in the pathogenicity.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category M Cell wall / membrane / envelope biogenesis
eggNOG descriptionCatalyzes the Claisen rearrangement of chorismate to prephenate
Orthologous groupCOG1605
EC number EC 5.4.99.5
KEGG orthology K04093
KEGG pathways map00400, map01100, map01110, map01130, map01230
KEGG modules M00024, M00025
Gene Ontology (18) GO:0003674, GO:0003824, GO:0004106, GO:0005575, GO:0005576, GO:0006082, GO:0008150, GO:0008152, GO:0009987, GO:0016853, GO:0016866, GO:0019752 +6 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 1.373 · diversifying/relaxed
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 3 missense, 1 nonsense, 0 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.37% of strains (537) · clonal

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
CM_2PF01817.27 2.1e-1241–109 Chorismate mutase type II

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

Closest characterised functional partner: fbpB (diacylglycerol acyltransferase/mycolyltransferase Ag85B), high confidence from genomic context alone (score 941 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2540c aroF chorismate synthase 974 965 coexpression:643 database:900
Rv1886c fbpB diacylglycerol acyltransferase/mycolyltransferase Ag85B 965 941 ctx neighborhood:771 coexpression:754 textmining:435
Rv3754 tyrA prephenate dehydrogenase TyrA 954 937 database:900
Rv3838c pheA prephenate dehydratase 937 909 database:900
Rv1609 trpE anthranilate synthase component I 910 905 database:900
Rv0948c chorismate mutase 979 901 database:900 textmining:803
Rv3215 entC isochorismate synthase 906 871 database:800
Rv0013 trpG anthranilate synthase component II 903 815 database:800 textmining:499
Rv2386c mbtI salicylate synthase 835 811 database:800
Rv1005c pabB para-aminobenzoate synthase component I 821 810 database:800
Rv2949c chorismate pyruvate-lyase 820 809 database:800
Rv0950c hyp hypothetical protein 804 804 coexpression:804
Rv1884c rpfC resuscitation-promoting factor RpfC 846 765 ctx neighborhood:762
Rv0709 rpmC 50S ribosomal protein L29 690 690 coexpression:680
Rv3227 aroA 3-phosphoshikimate 1-carboxyvinyltransferase 716 678 coexpression:660

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: chorismate mutase
  • MTBC0 PGAP product: chorismate mutase
  • Pfam (hmmscan --cut_ga): CM_2 PF01817.27 (E=2e-12)
  • (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_216401.1)
  • Domains: Pfam-A via hmmscan --cut_ga — CM_2 (PF01817.27)
  • 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 COG1605
  • Curated reference: UniProt P9WIB9 (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 — 71 functional partner(s); context anchor fbpB
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001999|Rv1885c|
MLTRPREIYLATAVSIGILLSLIAPLGPPLARADGTSQLAELVDAAAERLEVADPVAAFKWRAQLPIEDSGRVEQQLAKLGEDARSQHIDPDYVTRVFDDQIRATEAIEYSRFSDWKLNPASAPPEPPDLSASRSAIDSLNNRMLSQIWSHWSLLSAPSCAAQLDRAKRDIVRSRHLDSLYQRALTTATQSYCQALPPA