Rv2917 Family assigned · medium auto-curated

H37Rv Rv2917 · MTBC0 - · 626 aa · 3226363–3228243 (+) · RefSeq NP_217433.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotation
Revised (this work)Contains ResIII (PF04851.22), DEAD (PF00270.36), SWI2_SNF2 (PF18766.8) 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.

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 P9WL21 SwissProt · reviewed · Predicted
UniProt nameUncharacterized protein Rv2917

UniProt still lists this protein as Uncharacterized protein Rv2917; the revised annotation above is ahead of the current UniProt record.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category L Replication, recombination and repair
Preferred namesdrA
eggNOG descriptionType III restriction enzyme, res subunit
Orthologous groupCOG1061
Gene Ontology (6) GO:0005575, GO:0005623, GO:0005886, GO:0016020, 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 0.481 · purifying
Polymorphic sites (≥ 0.1% of strains) 6 synonymous, 8 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
ResIIIPF04851.22 1.5e-1565–218 Type III restriction enzyme, res subunit
DEADPF00270.36 3.0e-0869–217 DEAD/DEAH box helicase
SWI2_SNF2PF18766.8 7.2e-0889–274 SWI2/SNF2 ATPase

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv1329c dinG ATP-dependent helicase DinG 887 879 experimental:685 database:622
Rv0667 rpoB DNA-directed RNA polymerase subunit beta 855 853 experimental:578 database:621
Rv3457c rpoA DNA-directed RNA polymerase subunit alpha 852 853 experimental:627 database:621
Rv1390 rpoZ DNA-directed RNA polymerase subunit omega 847 847 experimental:613 database:621
Rv1629 polA DNA polymerase I 786 766 experimental:430 database:580
Rv2033c hyp hypothetical protein 754 755 ctx cooccurence:752
Rv2090 5'-3' exonuclease 765 752 experimental:430 database:580
Rv0668 rpoC DNA-directed RNA polymerase subunit beta' 747 686 database:620
Rv2529 hyp hypothetical protein 705 686 database:610
Rv2101 helZ helicase HelZ 692 669 database:615
Rv3258c hyp hypothetical protein 660 660 ctx cooccurence:660
Rv2256c hyp hypothetical protein 654 654 ctx cooccurence:654
Rv1334 mec [CysO 629 629 database:613
Rv3036c TB22.2 hyp hypothetical protein 620 621 database:563
Rv3812 PE_PGRS62 PE-PGRS family protein PE_PGRS62 620 621 database:563

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): hypothetical protein
  • Pfam (hmmscan --cut_ga): ResIII PF04851.22 (E=1e-15), DEAD PF00270.36 (E=3e-08), SWI2_SNF2 PF18766.8 (E=7e-08)
  • (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_217433.1)
  • Domains: Pfam-A via hmmscan --cut_ga — ResIII (PF04851.22), DEAD (PF00270.36), SWI2_SNF2 (PF18766.8)
  • 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 COG1061
  • Curated reference: UniProt P9WL21 (SwissProt, reviewed; Predicted)
  • 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 — 50 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv2917|
MRVTRLVDAESTRCDVGPAPKSVAMLHFTAATSRFRLGRERANSVRSDGGWGVLQPVSATFNPPLRGWQRRALVQYLGTQPRDFLAVATPGSGKTSFALRIAAELLRYHTVEQVTVVVPTEHLKVQWAHAAAAHGLSLDPKFANSNPQTSPEYHGVMVTYAQVASHPTLHRVRTEARKTLVVFDEIHHGGDAKTWGDAIREAFGDATRRLALTGTPFRSDDSPIPFVSYQPDADGVLRSQADHTYGYAEALADGVVRPVVFLAYSGQARWRDSAGEEYEARLGEPLSAEQTARAWRTALDPEGEWMPAVITAADRRLRQLRAHVPDAGGMIIASDRTTARAYARLLTTMTAEEPTVVLSDDPGSSARITEFAQGTSRWLVAVRMVSEGVDVPRLSVGVYATNASTPLFFAQAIGRFVRSRRPGETASIFVPSVPNLLQLASALEVQRNHVLGRPHRESAHDPLDGDPATRTQTERGGAERGFTALGADAELDQVIFDGSSFGTATPTGSDEEADYLGIPGLLDAEQMRALLHRRQDEQLRKRAQLQKGATQPATSGASASVHGQLRDLRRELHTLVSIAHHRTGKPHGWIHDERRRRCGGPPIAAATRAQIKARIDALRQLNSERS