PPE36 Family assigned · medium auto-curated

H37Rv Rv2108 · MTBC0 - · 243 aa · 2367711–2368442 (+) · RefSeq YP_177859.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)PPE family protein PPE36
MTBC0 PGAP re-annotation
Revised (this work)PPE family protein PPE36. Pfam: PPE (PF00823.26).

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 P9WI01 SwissProt · reviewed · Evidence at protein level
UniProt nameUncharacterized PPE family protein PPE36

UniProt still lists this protein as Uncharacterized PPE family protein PPE36; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category N Cell motility
eggNOG descriptionPPE family
Orthologous groupCOG5651

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 0.561 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 5 synonymous, 9 missense, 1 nonsense, 0 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.44% of strains (636) · 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
PPEPF00823.26 8.6e-593–164 PPE family

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

Closest characterised functional partner: PE22 (PE family protein PE22), medium confidence from genomic context alone (score 649 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1800 PPE28 PPE family protein PPE28 742 738 coexpression:738
Rv2107 PE22 PE family protein PE22 760 649 ctx neighborhood:649
Rv2431c PE25 PE family protein PE25 542 155 textmining:481
Rv0265c iron ABC transporter substrate-binding lipoprotein 442 57 textmining:433
Rv2123 PPE37 PPE family protein PPE37 409 51 textmining:403
Rv0266c oplA 5-oxoprolinase OplA 632 47 textmining:630
Rv1381 pyrC dihydroorotase 532 47 textmining:530
Rv3412 hyp hypothetical protein 532 46 textmining:530
Rv1383 carA carbamoyl-phosphate synthase small subunit 548 44 textmining:547
Rv0203 hyp hypothetical protein 475 44 textmining:474
Rv1386 PE15 PE family protein PE15 681 41 textmining:682
Rv3592 mhuD heme-degrading monooxygenase 549 41 textmining:549
Rv0966c hyp hypothetical protein 547 41 textmining:547
Rv0264c hyp hypothetical protein 461 41 textmining:461

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): PPE family protein PPE36
  • Pfam (hmmscan --cut_ga): PPE PF00823.26 (E=9e-59)
  • (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 YP_177859.1)
  • Domains: Pfam-A via hmmscan --cut_ga — PPE (PF00823.26)
  • 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 COG5651
  • Curated reference: UniProt P9WI01 (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 — 14 functional partner(s); context anchor PE22
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv2108|PPE36
MPNFWALPPEINSTRIYLGPGSGPILAAAQGWNALASELEKTKVGLQSALDTLLESYRGQSSQALIQQTLPYVQWLTTTAEHAHKTAIQLTAAANAYEQARAAMVPPAMVRANRVQTTVLKAINWFGQFSTRIADKEADYEQMWFQDALVMENYWEAVQEAIQSTSHFEDPPEMADDYDEAWMLNTVFDYHNENAKEEVIHLVPDVNKERGPIELVTKVDKEGTIRLVYDGEPTFSYKEHPKF