Rv1005c Resolved · high auto-curated

H37Rv Rv1005c · MTBC0 - · 458 aa · 1122222–1123598 (-) · RefSeq NP_215521.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)para-aminobenzoate synthase component I
MTBC0 PGAP re-annotation
Revised (this work)Para-aminobenzoate synthase component I. Pfam: Chorismate_bind (PF00425.25).

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

Annotated on the H37Rv protein: this gene has no 1:1 ancestral MTBC0 anchor (PE/PPE, paralogue, IS element, or otherwise unanchored CDS).

Curated reference (UniProt)

UniProt O05591 TrEMBL · unreviewed · Evidence at protein level
UniProt nameProbable para-aminobenzoate synthase component I PABD

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category H Coenzyme transport and metabolism
Q Secondary metabolites biosynthesis, transport and catabolism
Preferred namepabB
eggNOG descriptionsynthase component I
Orthologous groupCOG1169
EC number EC 2.6.1.85
KEGG orthology K01665
KEGG pathways map00790

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 0.761 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 5 missense, 1 nonsense, 0 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.15% of strains (221) · 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
Chorismate_bindPF00425.25 2.2e-66188–435 chorismate binding enzyme

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

Closest characterised functional partner: trpG (anthranilate synthase component II), high confidence from genomic context alone (score 1000 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv0013 trpG anthranilate synthase component II 999 1000 ctx fusion:900 cooccurence:769 coexpression:696 experimental:788 database:900
Rv2192c trpD anthranilate phosphoribosyltransferase 982 980 ctx cooccurence:725 coexpression:695 experimental:778
Rv1611 trpC indole-3-glycerol phosphate synthase 952 949 ctx cooccurence:744 coexpression:647 experimental:461
Rv0812 4-amino-4-deoxychorismate lyase 973 923 database:900 textmining:664
Rv2540c aroF chorismate synthase 918 910 ctx cooccurence:433 database:800
Rv1613 trpA tryptophan synthase subunit alpha 906 896 ctx cooccurence:707 coexpression:648
Rv1612 trpB tryptophan synthase subunit beta 898 888 ctx cooccurence:637 coexpression:692
Rv1609 trpE anthranilate synthase component I 856 856 database:800
Rv0948c chorismate mutase 822 811 database:800
Rv1885c chorismate mutase 821 810 database:800
Rv1435c hyp hypothetical protein 820 809 coexpression:648 experimental:461
Rv1006 hyp hypothetical protein 786 726 ctx neighborhood:725
Rv1004c membrane protein 650 636 ctx neighborhood:582
Rv3859c gltB glutamate synthase large subunit 549 533 ctx neighborhood:504
Rv3608c folP1 dihydropteroate synthase 580 517

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

  • Annotation from H37Rv (no MTBC0 1:1 anchor; H37Rv protein used): para-aminobenzoate synthase component I
  • Pfam (hmmscan --cut_ga): Chorismate_bind PF00425.25 (E=2e-66)
  • (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_215521.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Chorismate_bind (PF00425.25)
  • 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 COG1169
  • Curated reference: UniProt O05591 (TrEMBL, unreviewed; 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 — 31 functional partner(s); context anchor trpG
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv1005c|
MNLAWELSTRTKSPRSHLRCENPQFCQARTVRIDRLGDLGGAPAVLRAVGRATSRLDLPPPAALTGEWFGALAVIAPSVSIQPVSGDDVFSGPPGTGGPDATGAVGGGWVGYLSYPDAGADGRPHRIPEAAGGWTDCVLRRDRDGQWWYESLSGAPIADWLASALATTRASVARPAPACRIDWEPADRAAHRDGVLACLEAIGAGEVYQACVCTQFAGTVTGSPLDFFIDGFGRTAPSRSAFVAGPWGAVASLSPELFLRRRGSVVTSSPIKGTLPLDAPPSALRASAKEVAENIMIVDLVRNDLGRVAVTGTVTVPELLVVRPAPGVWHLVSTVSARVPLEEPMSALLDAAFPPASVTGTPKLRARQLISQWERYRRGIYCGTVGLASPVAGCELNVAIRTVEFDTAGNAVLGVGGGITADSDPDAEWAECLHKAAPIVGLPAATRTTPARLASKVR