Rv1582c Family assigned · medium auto-curated

H37Rv Rv1582c · MTBC0 mtbc0_001689 · 471 aa · 1796457–1797872 (-) · RefSeq NP_216098.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)phage protein
MTBC0 PGAP re-annotationphage/plasmid primase%2C P4 family
Revised (this work)Phage/plasmid primase%2C P4 family. Pfam: D5_N (PF08706.17), DUF5906 (PF19263.6).

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

Curated reference (UniProt)

UniProt O06608 TrEMBL · unreviewed · Predicted
UniProt nameProbable PhiRv1 phage protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category L Replication, recombination and repair
eggNOG descriptionD5 N terminal like
Orthologous groupCOG3378
KEGG orthology K06919

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, 1 nonsense, 0 frameshift
Disruption 1 distinct premature-stop/frameshift site(s); most common in 0.10% of strains (150) · 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
D5_NPF08706.17 1.8e-3541–185 D5 N terminal like
DUF5906PF19263.6 1.7e-07214–328 Family of unknown function (DUF5906)

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

Closest characterised functional partner: Rv1583c (phage protein), high confidence from genomic context alone (score 779 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1583c phage protein 780 779 ctx neighborhood:777
Rv1584c phage protein 777 777 ctx neighborhood:773
Rv1586c phage integrase 802 757 ctx neighborhood:634
Rv1585c phage protein 628 628 ctx neighborhood:605
Rv1587c hyp hypothetical protein 630 627 ctx neighborhood:617
Rv1588c hyp hypothetical protein 622 619 ctx neighborhood:617
Rv1576c phage capsid protein 597 597 ctx cooccurence:444
Rv1578c phage protein 583 583
Rv2650c prophage protein 524 524 ctx cooccurence:468
Rv1581c phage protein 455 455 ctx neighborhood:447
Rv1579c phage protein 445 445 ctx neighborhood:436
Rv1580c phage protein 443 442 ctx neighborhood:436
Rv2351c plcA membrane-associated phospholipase A 512 44 textmining:511
Rv3878 espJ ESX-1 secretion-associated protein EspJ 542 42 textmining:542
Rv3879c espK ESX-1 secretion-associated protein EspK 511 41 textmining:511

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: phage protein
  • MTBC0 PGAP product: phage/plasmid primase%2C P4 family
  • Pfam (hmmscan --cut_ga): D5_N PF08706.17 (E=2e-35), DUF5906 PF19263.6 (E=2e-07)
  • (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_216098.1)
  • Domains: Pfam-A via hmmscan --cut_ga — D5_N (PF08706.17), DUF5906 (PF19263.6)
  • 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 COG3378
  • Curated reference: UniProt O06608 (TrEMBL, unreviewed; 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 — 15 functional partner(s); context anchor Rv1583c
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001689|Rv1582c|
MADIPYGTDYPDAPWIDRDGHVLIDDGGKPTQVHRGQARIAYRLAERYQDKLLHVAGIGWHSWDGRRWAADDRGEAKRAVLAELRQALSDSLNDKELRADVRKCESASGVAGVLDLAAALVPFAATVADLDSDPHLLNVANGTLDLHTLKLRPHAPADRITKICRGAYQSDTESPLWQAFLTRVLPDEGVRGFVQRLAGVGLLGTVREHVLAILIGVGANGKSVFDKAIRYALGDYACTAEPDLFMHRENAHPTGEMDLRGVRWVAVSESEKDRRLAESTIKRLTGGDTIRARKMRQDFVEFTPSHTPLLITNHLPRVPGDDTAIWRRIRVVPFEVVIPADEQDRELDARLQLEADSILSWAVAGWSDYQRIGLSQPDAVLAATSNYREDSDTIKRFIDDECVTSSPVLKATTTHLFEAWQRWRVQEGVPEISRKAFGQSLDTHGYPVTDKARDGRWRAGIAVRGADDFDD