priA Family assigned · medium auto-curated

H37Rv Rv1402 · MTBC0 - · 655 aa · 1577613–1579580 (+) · RefSeq NP_215918.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)primosomal protein N'
MTBC0 PGAP re-annotation
Revised (this work)Primosomal protein N'. Pfam: PriA_3primeBD (PF17764.7), PriA_C_2 (PF27106.1).

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 P9WMQ9 SwissProt · reviewed · Evidence at protein level
UniProt nameProbable replication restart protein PriA
Curated functionInitiates the restart of stalled replication forks, which reloads the replicative helicase on sites other than the origin of replication. Recognizes and binds to abandoned replication forks and remodels them to uncover a helicase loading site. Promotes assembly of the primosome at these replication forks.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category L Replication, recombination and repair
Preferred namepriA
eggNOG descriptionInvolved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA
Orthologous groupCOG1198
KEGG orthology K04066
KEGG pathways map03440
Gene Ontology (64) GO:0003674, GO:0003678, GO:0003824, GO:0004003, GO:0004386, GO:0005575, GO:0005623, GO:0005886, GO:0006139, GO:0006259, GO:0006260, GO:0006261 +52 more

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 0.268 · purifying
Polymorphic sites (≥ 0.1% of strains) 9 synonymous, 6 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
PriA_3primeBDPF17764.7 2.8e-172–96 3'DNA-binding domain (3'BD)
PriA_C_2PF27106.1 8.2e-18556–655 PriA, C-terminal domain

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

Closest characterised functional partner: Rv1401 (membrane protein), high confidence from genomic context alone (score 795 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv0054 ssb single-strand DNA-binding protein 865 818 experimental:787
Rv1401 membrane protein 795 795 ctx neighborhood:784
Rv2478c hyp hypothetical protein 812 792 experimental:787
Rv1406 fmt methionyl-tRNA formyltransferase 762 762 coexpression:613
Rv1391 dfp bifunctional phosphopantothenoylcysteine decarboxylase/phosphopantothenate--cysteine ligase 716 717 coexpression:648
Rv0051 transmembrane protein 696 696 ctx cooccurence:693
Rv1399c nlhH carboxylesterase NlhH 682 683 ctx neighborhood:678
Rv1423 whiA transcriptional regulator WhiA 678 678 ctx cooccurence:597
Rv3404c hyp hypothetical protein 655 655 coexpression:613
Rv1407 fmu 16S rRNA m5C967 methyltransferase 631 632 coexpression:424
Rv3201c adnB ATP-dependent DNA helicase 647 631 ctx cooccurence:590
Rv0955 integral membrane protein 622 623 ctx cooccurence:619
Rv0058 dnaB replicative DNA helicase 718 603
Rv3604c transmembrane protein 593 594 ctx cooccurence:591
Rv2343c dnaG DNA primase 582 556

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): primosomal protein N'
  • Pfam (hmmscan --cut_ga): PriA_3primeBD PF17764.7 (E=3e-17), PriA_C_2 PF27106.1 (E=8e-18)
  • (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_215918.1)
  • Domains: Pfam-A via hmmscan --cut_ga — PriA_3primeBD (PF17764.7), PriA_C_2 (PF27106.1)
  • 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 COG1198
  • Curated reference: UniProt P9WMQ9 (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 — 45 functional partner(s); context anchor Rv1401
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv1402|priA
MLSVPHLDRDFDYLVPAEHSDDAQPGVRVRVRFHGRLVDGFVLERRSDSDHHGKLGWLDRVVSPEPVLTTEIRRLVDAVAARYAGTRQDVLRLAVPARHARVEREITTAPGRPVVAPVDPSGWAAYGRGRQFLAALADSRAARAVWQALPGELWADRFAEAAAQTVRAGRTVLAIVPDQRDLDTLWQAATALVDEHSVVALSAGLGPEARYRRWLAALRGSARLVIGTRSAVFAPLSELGLVMVWADADDSLAEPRAPYPHAREVAMLRAHQARCAALIGGYARTAEAHALVRSGWAHDVVAPRPEVRARSPRVVALDDSGYDDARDPAARTARLPSIALRAARSALQSGAPVLVQVPRRGYIPSLACGRCRAIARCRSCTGPLSLQGAGSPGAVCRWCGRVDPTLRCVRCGSDVVRAVVVGARRTAEELGRAFPGTAVITSAGDTLVPQLDAGPALVVATPGAEPRAPGGYGAALLLDSWALLGRQDLRAAEDALWRWMTAAALVRPRGAGGVVTVVAESSIPTVQSLIRWDPVGHAEAELAARTEVGLPPSVHIAALDGPAGTVTALLEAARLPDPDRLQADLLGPVDLPPGVRRPAGIPADAPVIRMLLRVCREQGLELAASLRRGIGVLSARQTRQTRSLVRVQIDPLHIG