dinG Resolved · high auto-curated

H37Rv Rv1329c · MTBC0 mtbc0_001426 · 664 aa · 1507897–1509891 (-) · RefSeq NP_215845.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)ATP-dependent helicase DinG
MTBC0 PGAP re-annotationATP-dependent helicase DinG
Revised (this work)ATP-dependent helicase DinG. Pfam: DEAD (PF00270.36), Helicase_C_2 (PF13307.13).

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

Curated reference (UniProt)

UniProt P9WMR5 SwissProt · reviewed · Evidence at protein level
UniProt nameATP-dependent helicase DinG
EC (curated) EC 5.6.2.3
Curated functionA structure-dependent 5'-3' DNA helicase that unwinds a number of substrates that resemble intermediates in DNA repair, recombination and replication. Translocates on ssDNA with 5'-3' polarity..; FUNCTION: Unwinds G4 DNA (planar arrays of 4 guanine bases stabilized by hydrogen bonds) with both 5'- and 3'- ss-tails.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category K Transcription
L Replication, recombination and repair
Preferred namedinG
eggNOG descriptionhelicase
Orthologous groupCOG1199
EC number EC 3.6.4.12
KEGG orthology K03722
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 1.539 · diversifying/relaxed
Polymorphic sites (≥ 0.1% of strains) 2 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
DEADPF00270.36 4.9e-0734–89 DEAD/DEAH box helicase
Helicase_C_2PF13307.13 3.7e-33479–639 Helicase C-terminal domain

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

Closest characterised functional partner: mec ([CysO), high confidence from genomic context alone (score 948 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1390 rpoZ DNA-directed RNA polymerase subunit omega 977 976 experimental:854 database:844
Rv3457c rpoA DNA-directed RNA polymerase subunit alpha 973 971 experimental:824 database:844
Rv0667 rpoB DNA-directed RNA polymerase subunit beta 971 968 experimental:801 database:844
Rv1334 mec [CysO 950 948 ctx neighborhood:750 database:774
Rv1277 hyp hypothetical protein 930 919 experimental:771 database:639
Rv1629 polA DNA polymerase I 955 897 experimental:721 database:621 textmining:580
Rv1179c hyp hypothetical protein 892 884 experimental:685 database:622
Rv0861c ercc3 DNA helicase Ercc3 948 882 experimental:685 database:622 textmining:580
Rv1947 hyp hypothetical protein 890 881 experimental:685 database:622
Rv1961 hyp hypothetical protein 888 879 experimental:685 database:622
Rv2917 hyp hypothetical protein 887 879 experimental:685 database:622
Rv2101 helZ helicase HelZ 942 869 database:812 textmining:578
Rv0668 rpoC DNA-directed RNA polymerase subunit beta' 859 845 database:844
Rv1330c pncB1 nicotinic acid phosphoribosyltransferase PncB1 830 830 ctx neighborhood:817
Rv2090 5'-3' exonuclease 819 796 experimental:469 database:621

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: ATP-dependent helicase DinG
  • MTBC0 PGAP product: ATP-dependent helicase DinG
  • Pfam (hmmscan --cut_ga): DEAD PF00270.36 (E=5e-07), Helicase_C_2 PF13307.13 (E=4e-33)
  • (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_215845.1)
  • Domains: Pfam-A via hmmscan --cut_ga — DEAD (PF00270.36), Helicase_C_2 (PF13307.13)
  • 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 COG1199
  • Curated reference: UniProt P9WMR5 (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 — 140 functional partner(s); context anchor mec
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001426|Rv1329c|dinG
MSESVSMSVPELLAIAVAALGGTRRRGQQEMAAAVAHAFETGEHLVVQAGTGTGKSLAYLVPAIIRALCDDAPVVVSTATIALQRQLVDRDLPQLVDSLTNALPRRPKFALLKGRRNYLCLNKIHNSVTASDHDDERPQEELFDPVAVTALGRDVQRLTAWASTTVSGDRDDLKPGVGDRSWSQVSVSARECLGVARCPFGSECFSERARGAAGLADVVVTNHALLAIDAVAESAVLPEHRLLVVDEAHELADRVTSVAAAELTSATLGMAARRITRLVDPKVTQRLQAASATFSSAIHDARPGRIDCLDDEMATYLSALRDAASAARSAIDTGSDTTTASVRAEAGAVLTEISDTASRILASFAPAIPDRSDVVWLEHEDNHESARAVLRVAPLSVAELLATQVFARATTVLTSATLTIGGSFDAMATAWGLTADTPWRGLDVGSPFQHAKSGILYVAAHLPPPGRDGSGSAEQLTEIAELITAAGGRTLGLFSSMRAARAATEAMRERLSTPVLCQGDDSTSTLVEKFTADAATSLFGTLSLWQGVDVPGPSLSLVLIDRIPFPRPDDPLLSARQRAVAARGGNGFMTVAASHAALLLAQGSGRLLRRVTDRGVVAVLDSRMATARYGEFLRASLPPFWQTTNATQVRAALRRLARADAKAH