oppD Family assigned · medium auto-curated

H37Rv Rv1281c · MTBC0 mtbc0_001371 · 612 aa · 1442416–1444254 (-) · RefSeq NP_215797.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)oligopeptide ABC transporter ATP-binding protein OppD
MTBC0 PGAP re-annotationABC transporter ATP-binding protein
Revised (this work)ABC transporter ATP-binding protein. Pfam: oligo_HPY (PF08352.18), ABC_tran (PF00005.34).

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

Curated reference (UniProt)

UniProt P9WQJ5 SwissProt · reviewed · Evidence at protein level
UniProt nameOligopeptide transport ATP-binding protein OppD
EC (curated) EC 7.4.2.6
Curated functionPart of the ABC transporter complex OppABCD involved in the uptake of oligopeptides. Responsible for energy coupling to the transport system. Glutathione (GSH) uptake by mycobacteria through the OppABCD system contributes to the depletion of the GSH pool in infected macrophages, which impairs the ability of the macrophage to detoxify methylglyoxal (MG) and contributes to enhanced production of inflammatory cytokines. May also promote Mn(2+) uptake.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category P Inorganic ion transport and metabolism
Preferred nameoppD
eggNOG descriptionBelongs to the ABC transporter superfamily
Orthologous groupCOG1123
KEGG orthology K02031, K02032
KEGG pathways map02024
KEGG modules M00239
Gene Ontology (8) GO:0005575, GO:0005618, GO:0005623, GO:0005886, GO:0016020, GO:0030312, GO:0044464, GO:0071944

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 0.68 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 6 synonymous, 11 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
oligo_HPYPF08352.18 3.8e-16234–299 Oligopeptide/dipeptide transporter, C-terminal region
ABC_tranPF00005.34 6.8e-32378–527 ABC transporter

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

Closest characterised functional partner: oppC (oligopeptide ABC transporter permease OppC), high confidence from genomic context alone (score 999 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1282c oppC oligopeptide ABC transporter permease OppC 999 999 ctx neighborhood:806 fusion:796 cooccurence:774 database:900
Rv1283c oppB oligopeptide ABC transporter permease OppB 998 997 ctx neighborhood:816 cooccurence:773 coexpression:404 database:900
Rv1280c oppA oligopeptide ABC transporter substrate-binding lipoprotein OppA 993 993 ctx neighborhood:802 cooccurence:617 database:900
Rv3664c dppC dipeptide ABC transporter permease DppC 978 971 ctx fusion:822 cooccurence:769
Rv2585c lipoprotein 916 916 database:900
Rv3663c dppD dipeptide ABC transporter ATP-binding protein DppD 917 915 database:900
Rv3665c dppB dipeptide ABC transporter permease DppB 877 864 ctx cooccurence:761
Rv1284 canA beta-carbonic anhydrase 506 506 ctx neighborhood:505
Rv3666c dppA dipeptide ABC transporter substrate-binding lipoprotein DppA 621 465

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: oligopeptide ABC transporter ATP-binding protein OppD
  • MTBC0 PGAP product: ABC transporter ATP-binding protein
  • Pfam (hmmscan --cut_ga): oligo_HPY PF08352.18 (E=4e-16), ABC_tran PF00005.34 (E=7e-32)
  • (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_215797.1)
  • Domains: Pfam-A via hmmscan --cut_ga — oligo_HPY (PF08352.18), 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 COG1123
  • Curated reference: UniProt P9WQJ5 (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 — 9 functional partner(s); context anchor oppC
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001371|Rv1281c|oppD
MSPLLEVTDLAVTFRTDGDPVTAVRGISYRVEPGEVVAMVGESGSGKSAAAMAVVGLLPEYAQVRGSVRLQGTELLGLADNAMSRFRGKAIGTVFQDPMSALTPVYTVGDQIAEAIEVHQPRVGKKAARRRAVELLDLVGISQPQRRSRAFPHELSGGERQRVVIAIAIANDPDLLICDEPTTALDVTVQAQILDVLKAARDVTGAGVLIITHDLGVVAEFADRALVMYAGRVVESAGVNDLYRDRRMPYTVGLLGSVPRLDAAQGTRLVPIPGAPPSLAGLAPGCPFAPRCPLVIDECLTAEPELLDVATDHRAACIRTELVTGRSAADIYRVKTEARPAALGDASVVVRVRHLVKTYRLAKGVVLRRAIGEVRAVDGISLELRQGRTLGIVGESGSGKSTTLHEILELAAPQSGSIEVLGTDVATLGTAERRSLRRDIQVVFQDPVASLDPRLPVFDLIAEPLQANGFGKNETHARVAELLDIVGLRHGDASRYPAEFSGGQKQRIGIARALALQPKILALDEPVSALDVSIQAGIINLLLDLQEQFGLSYLFVSHDLSVVKHLAHQVAVMLAGTVVEQGDSEEVFGNPKHEYTRRLLGAVPQPDPARRG