Rv3115 Resolved · high auto-curated

H37Rv Rv3115 · MTBC0 - · 415 aa · 3481451–3482698 (+) · RefSeq NP_217631.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)transposase
MTBC0 PGAP re-annotation
Revised (this work)Transposase. Pfam: Transposase_mut (PF00872.25).

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 P96354 TrEMBL · unreviewed · Inferred from homology
UniProt nameMutator family transposase
Curated functionRequired for the transposition of the insertion element.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category L Replication, recombination and repair
eggNOG descriptionTransposase, mutator
Orthologous groupCOG3328
KEGG orthology K07493

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, 1 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
Transposase_mutPF00872.25 1.2e-1561–379 Transposase, Mutator family

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

Closest characterised functional partner: moeB2 (molybdenum cofactor biosynthesis protein MoeB), medium confidence from genomic context alone (score 558 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv2512c insertion sequence element IS1081 transposase 860 861 coexpression:860
Rv1199c insertion sequence element IS1081 transposase 860 861 coexpression:860
Rv1047 transposase 860 861 coexpression:860
Rv3023c transposase 839 840 coexpression:839
Rv2666 Probable transposase for insertion sequence element IS1081 (fragment); Required for the transposition of the insertion element. 803 803 coexpression:802
Rv3116 moeB2 molybdenum cofactor biosynthesis protein MoeB 558 558 ctx neighborhood:558
Rv3118 sseC1 hyp hypothetical protein 499 500 ctx neighborhood:495
Rv3117 cysA3 thiosulfate sulfurtransferase 498 498 ctx neighborhood:495
Rv3114 hyp hypothetical protein 467 467 ctx neighborhood:467
Rv3120 hyp hypothetical protein 460 461 ctx neighborhood:459
Rv3119 moaE1 molybdopterin synthase catalytic subunit 1 459 459 ctx neighborhood:459
Rv3113 phosphatase 443 443 ctx neighborhood:443

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): transposase
  • Pfam (hmmscan --cut_ga): Transposase_mut PF00872.25 (E=1e-156)
  • (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_217631.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Transposase_mut (PF00872.25)
  • 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 COG3328
  • Curated reference: UniProt P96354 (TrEMBL, unreviewed; Inferred from homology)
  • 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 — 12 functional partner(s); context anchor moeB2
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv3115|
MTSSHLIDAEQLLADQLAQASPDLLRGLLSTFIAALMGAEADALCGAGYRERSDERSNQRNGYRHRDFDTRAATIDVAIPKLRQGSYFPDWLLQRRKRAERALTSVVATCYLLGVSTRRMERLVETLGVTKLSKSQVSIMAKELDEAVEAFRTRPLDAGPYTFLAADALVLKVREAGRVVGVHTLIATGVNAEGYREILGIQVTSAEDGAGWLAFFRDLVARGLSGVALVTSDAHAGLVAAIGATLPAAAWQRCRTHYAANLMAATPKPSWPWVRTLLHSIYDQPDAESVVAQYDRVLDALTDKLPAVAEHLDTARTDLLAFTAFPKQIWRQIWSNNPQERLNREVRRRTDVVGIFPDRASIIRLVGAVLAEQHDEWIEGRRYLGLEVLTRARAALTSTEEPAKQQTTNTPALTT