tatD Resolved · high auto-curated

H37Rv Rv1008 · MTBC0 - · 264 aa · 1127089–1127883 (+) · RefSeq NP_215524.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)deoxyribonuclease TatD
MTBC0 PGAP re-annotation
Revised (this work)Deoxyribonuclease TatD. Pfam: TatD_DNase (PF01026.28).

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 O08343 SwissProt · reviewed · Evidence at protein level
UniProt nameUncharacterized metal-dependent hydrolase TatD
EC (curated) EC 3.1.-.-

UniProt still lists this protein as Uncharacterized metal-dependent hydrolase TatD; 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 nametatD
eggNOG descriptionTatD family
Orthologous groupCOG0084
KEGG orthology K03424
Gene Ontology (41) GO:0003674, GO:0003824, GO:0004518, GO:0004536, GO:0005575, GO:0005623, GO:0005886, GO:0006139, GO:0006259, GO:0006308, GO:0006725, GO:0006807 +29 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 0.358 · purifying
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 3 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
TatD_DNasePF01026.28 6.8e-762–258 TatD related DNase

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

Closest characterised functional partner: metS (methionine--tRNA ligase), high confidence from genomic context alone (score 970 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1007c metS methionine--tRNA ligase 969 970 ctx neighborhood:783 fusion:723
Rv1010 ksgA rRNA small subunit methyltransferase A 958 775 ctx neighborhood:734 textmining:821
Rv1009 rpfB resuscitation-promoting factor RpfB 913 736 ctx neighborhood:734 textmining:687
Rv2404c lepA GTP-binding protein LepA 508 508 ctx cooccurence:483
Rv1011 ispE 4-diphosphocytidyl-2C-methyl-D-erythritol kinase 850 463 ctx neighborhood:461 textmining:733
Rv2478c hyp hypothetical protein 447 448 coexpression:416
Rv0054 ssb single-strand DNA-binding protein 446 447 coexpression:415
Rv3834c serS serine--tRNA ligase 440 440
Rv3419c gcp O-sialoglycoprotein endopeptidase 430 430 ctx cooccurence:423
Rv1112 ychF GTP-binding protein 427 425
Rv2165c rsmH rRNA small subunit methyltransferase H 422 423 ctx cooccurence:413
Rv2925c rnc ribonuclease III 416 417
Rv0986 adhesion component ABC transporter ATP-binding protein 413 414
Rv2440c obg GTPase Obg 427 392
Rv2902c rnhB ribonuclease HII 555 370

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): deoxyribonuclease TatD
  • Pfam (hmmscan --cut_ga): TatD_DNase PF01026.28 (E=7e-76)
  • (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_215524.1)
  • Domains: Pfam-A via hmmscan --cut_ga — TatD_DNase (PF01026.28)
  • 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 COG0084
  • Curated reference: UniProt O08343 (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 — 32 functional partner(s); context anchor metS
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv1008|tatD
MVDAHTHLDACGARDADTVRSLVERAAAAGVTAVVTVADDLESARWVTRAAEWDRRVYAAVALHPTRADALTDAARAELERLVAHPRVVAVGETGIDMYWPGRLDGCAEPHVQREAFAWHIDLAKRTGKPLMIHNRQADRDVLDVLRAEGAPDTVILHCFSSDAAMARTCVDAGWLLSLSGTVSFRTARELREAVPLMPVEQLLVETDAPYLTPHPHRGLANEPYCLPYTVRALAELVNRRPEEVALITTSNARRAYGLGWMRQ