Rv2326c Family assigned · medium auto-curated

H37Rv Rv2326c · MTBC0 - · 697 aa · 2597854–2599947 (-) · RefSeq NP_216842.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)ABC transporter ATP-binding protein
MTBC0 PGAP re-annotation
Revised (this work)ABC transporter ATP-binding protein. Pfam: ABC_tran (PF00005.34).

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 P9WQI7 SwissProt · reviewed · Evidence at protein level
UniProt nameUncharacterized ABC transporter ATP-binding protein Rv2326c

UniProt still lists this protein as Uncharacterized ABC transporter ATP-binding protein Rv2326c; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category P Inorganic ion transport and metabolism
eggNOG descriptionABC transporter
Orthologous groupCOG1122
KEGG orthology K16785, K16786, K16787
KEGG pathways map02010
KEGG modules M00582
Gene Ontology (14) GO:0005575, GO:0005618, GO:0005623, GO:0005886, GO:0005887, GO:0016020, GO:0016021, GO:0030312, GO:0031224, GO:0031226, GO:0044425, GO:0044459 +2 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 0.538 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 7 synonymous, 10 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
ABC_tranPF00005.34 3.1e-22268–401 ABC transporter

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

Closest characterised functional partner: Rv1610 (membrane protein), medium confidence from genomic context alone (score 684 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2325c hyp hypothetical protein 999 999 ctx neighborhood:882 cooccurence:731 coexpression:901 experimental:652
Rv2327 hyp hypothetical protein 799 799 ctx neighborhood:789
Rv1125 hyp hypothetical protein 761 752 ctx cooccurence:750
Rv0408 pta phosphate acetyltransferase 708 708 coexpression:705
Rv1610 membrane protein 776 684 ctx cooccurence:674
Rv3666c dppA dipeptide ABC transporter substrate-binding lipoprotein DppA 705 666
Rv3707c hyp hypothetical protein 630 631 ctx cooccurence:626
Rv0383c ttfA hyp hypothetical protein 616 616 ctx cooccurence:616
Rv2397c cysA1 sulfate ABC transporter ATP-binding protein CysA 607 608
Rv1836c hyp hypothetical protein 595 596 ctx cooccurence:584
Rv1283c oppB oligopeptide ABC transporter permease OppB 623 588 coexpression:472
Rv1282c oppC oligopeptide ABC transporter permease OppC 723 572 coexpression:455
Rv0428c GCN5-like N-acetyltransferase 565 566 ctx cooccurence:552
Rv3035 hyp hypothetical protein 565 566 ctx cooccurence:548
Rv1238 sugC sugar ABC transporter ATP-binding protein SugC 563 564 database:540

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): ABC transporter ATP-binding protein
  • Pfam (hmmscan --cut_ga): ABC_tran PF00005.34 (E=3e-22)
  • (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_216842.1)
  • Domains: Pfam-A via hmmscan --cut_ga — ABC_tran (PF00005.34)
  • 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 COG1122
  • Curated reference: UniProt P9WQI7 (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 — 59 functional partner(s); context anchor Rv1610
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv2326c|
MCCAVCGPEPGRIGEVTPLGPCPAQHRGGPLRPSELAQASVMAALCAVTAIISVVVPFAAGLALLGTVPTGLLAYRYRLRVLAAATVAAGMIAFLIAGLGGFMGVVHSAYIGGLTGIVKRRGRGTPTVVVSSLIGGFVFGAAMVGMLAAMVRLRHLIFKVMTANVDGIAATLARMHMQGAAADVKRYFAEGLQYWPWVLLGYFNIGIMIVSLIGWWALSRLLERMRGIPDVHKLDPPPGDDVDALIGPVPVRLDKVRFRYPRAGQDALREVSLDVRAGEHLAIIGANGSGKTTLMLILAGRAPTSGTVDRPGTVGLGKLGGTAVVLQHPESQVLGTRVADDVVWGLPLGTTADVGRLLSEVGLEALAERDTGSLSGGELQRLALAAALAREPAMLIADEVTTMVDQQGRDALLAVLSGLTQRHRTALVHITHYDNEADSADRTLSLSDSPDNTDMVHTAAMPAPVIGVDQPQHAPALELVGVGHEYASGTPWAKTALRDINFVVEQGDGVLIHGGNGSGKSTLAWIMAGLTIPTTGACLLDGRPTHEQVGAVALSFQAARLQLMRSRVDLEVASAAGFSASEQDRVAAALTVVGLDPALGARRIDQLSGGQMRRVVLAGLLARAPRALILDEPLAGLDAASQRGLLRLLEDLRRARGLTVVVVSHDFAGMEELCPRTLHLRDGVLESAAASEAGGMS