Rv0047c Family assigned · medium

H37Rv Rv0047c · MTBC0 mtbc0_000052 · 180 aa · 51284–51826 (-) · RefSeq NP_214561.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationPadR family transcriptional regulator
Revised (this work)PadR-family transcriptional regulator (Pfam PadR, PF03551). PadR repressors typically control detoxification and multidrug/stress-response genes; the regulon governed by this locus in M. tuberculosis is not established.

Curated reference (UniProt)

UniProt P71704 TrEMBL · unreviewed · Evidence at protein level
UniProt nameConserved protein

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

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category K Transcription
eggNOG descriptionTranscriptional regulator
Orthologous groupCOG1695

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 0.701 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 1 synonymous, 2 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
PadRPF03551.21 3.5e-216–81 Transcriptional regulator PadR-like family

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

Closest characterised functional partner: ino1 (inositol-3-phosphate synthase), high confidence from genomic context alone (score 841 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv0046c ino1 inositol-3-phosphate synthase 959 841 ctx neighborhood:802 textmining:755
Rv0044c oxidoreductase 726 727 ctx neighborhood:725
Rv0045c hydrolase 680 680 ctx neighborhood:675
Rv0043c HTH-type transcriptional regulator 633 630 ctx neighborhood:625
Rv0048c membrane protein 602 602 ctx neighborhood:602
Rv0049 hyp hypothetical protein 500 500 ctx neighborhood:499
Rv2936 drrA daunorubicin ABC transporter ATP-binding protein DrrA 445 445
Rv1218c tetronasin ABC transporter ATP-binding protein 440 440
Rv2937 drrB daunorubicin ABC transporter permease DrrB 436 437 ctx cooccurence:411
Rv3364c hyp hypothetical protein 422 422 ctx cooccurence:421
Rv1687c ABC transporter ATP-binding protein 419 420
Rv1747 ABC transporter ATP-binding protein/permease 574 374
Rv0037c MFS-type transporter 566 279 textmining:424
Rv1683 bifunctional long-chain acyl-CoA synthase/lipase 676 78 textmining:664
Rv2011c hyp hypothetical protein 878 67 textmining:875

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

  • MTBC0 PGAP product: 'PadR family transcriptional regulator'
  • Pfam: PadR PF03551 (E=3.5e-21) -- winged-helix-turn-helix repressor family

ESM Atlas signal (exploratory)

Ancestral protein hash 426716992f8cf5087fd0ef88029140fc · 10 ESM-space neighbours (max similarity 0.919). SAE features are orienting indices, not validated domains.

#IndexActivationInterpretation
16507 0.97 HTH and winged-helix DNA-binding domains
212403 0.81 Amphipathic coiled-coil dimerization helices
311889 0.69 Post-HTH hinge helix
414950 0.69 N-terminal HTH DNA-binding core
510186 0.65 wHTH beta-hairpin wing
69164 0.64 Secondary-structure N-capping motifs
72415 0.58 Basic HTH DNA-recognition helices
81235 0.57 Glycine-rich nucleic-acid-binding loops

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_214561.1)
  • Domains: Pfam-A via hmmscan --cut_ga — PadR (PF03551.21)
  • 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 COG1695
  • Curated reference: UniProt P71704 (TrEMBL, unreviewed; 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 — 22 functional partner(s); context anchor ino1
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000052|Rv0047c|
MLELAILGLLIESPMHGYELRKRLTGLLGAFRAFSYGSLYPALRRMQADGLIAENAAPAGTPVRRARRVYQLTDKGRRRFGELVADTGPHNYTDDGFGVHLAFFNRTPAEARMRILEGRRRQVEERREGLREAVARASSSFDRYTRQLHQLGLESSEREVKWLNELIAAERAAPNPAEQT