lpqE Family assigned · medium auto-curated

H37Rv Rv3584 · MTBC0 mtbc0_003803 · 182 aa · 4049507–4050055 (+) · RefSeq NP_218101.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)lipoprotein LpqE
MTBC0 PGAP re-annotationhypothetical protein
Revised (this work)Contains LpqE-like (PF04314.19) domain(s); putative function inferred from the domain architecture.

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

Curated reference (UniProt)

UniProt P9WK63 SwissProt · reviewed · Evidence at protein level
UniProt namePutative lipoprotein LpqE

UniProt still lists this protein as Putative lipoprotein LpqE; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category S Function unknown
Preferred namelpqE
eggNOG descriptionCopper chaperone PCu(A)C
Orthologous groupCOG2847
Gene Ontology (9) GO:0005575, GO:0005576, 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 n/a
Polymorphic sites (≥ 0.1% of strains) 0 synonymous, 2 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
LpqE-likePF04314.19 6.2e-2656–173 Putative lipoprotein LpqE-like

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

Closest characterised functional partner: Rv2876 (transmembrane protein), high confidence from genomic context alone (score 955 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2876 transmembrane protein 954 955 ctx cooccurence:541 experimental:902
Rv3043c ctaD cytochrome C oxidase cytochrome 1 924 924 experimental:902
Rv2195 qcrA ubiquinol-cytochrome C reductase rieske iron-sulfur subunit 960 921 experimental:902 textmining:518
Rv2200c ctaC cytochrome C oxidase subunit II 919 919 experimental:902
Rv2194 qcrC ubiquinol-cytochrome C reductase cytochrome subunit C 962 913 experimental:902 textmining:592
Rv2196 qcrB ubiquinol-cytochrome C reductase cytochrome subunit B 944 907 experimental:902 textmining:428
Rv2199c ctaF cytochrome c oxidase polypeptide 4 898 895 experimental:889
Rv2193 ctaE cytochrome C oxidase subunit III 872 872 experimental:855
Rv0432 sodC superoxide dismutase 823 824 experimental:790
Rv3586 disA DNA integrity scanning protein DisA 809 797 ctx neighborhood:796
Rv3850 hyp hypothetical protein 732 733 ctx cooccurence:729
Rv1546 hyp hypothetical protein 731 731 ctx cooccurence:730
Rv0513 transmembrane protein 719 719 ctx cooccurence:715
Rv0996 transmembrane protein 718 718 ctx cooccurence:717
Rv0910 toxin 709 710 ctx cooccurence:707

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: lipoprotein LpqE
  • MTBC0 PGAP product: hypothetical protein
  • Pfam (hmmscan --cut_ga): LpqE-like PF04314.19 (E=6e-26)
  • (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_218101.1)
  • Domains: Pfam-A via hmmscan --cut_ga — LpqE-like (PF04314.19)
  • 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 COG2847
  • Curated reference: UniProt P9WK63 (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 — 110 functional partner(s); context anchor Rv2876
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_003803|Rv3584|lpqE
MNRCNIRLRLAGMTTWVASIALLAAALSGCGAGQISQTANQKPAVNGNRLTINNVLLRDIRIQAVQTSDFIQPGKAVDLVLVAVNQSPDVSDRLVGITSDIGSVTVAGDARLPASGMLFVGTPDGQIVAPGPLPSNQAAKATVNLTKPIANGLTYNFTFKFEKAGQGSVMVPISAGLATPHE