Rv1453 Family assigned · medium auto-curated

H37Rv Rv1453 · MTBC0 mtbc0_001555 · 421 aa · 1648133–1649398 (+) · RefSeq NP_215969.2

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)transcriptional activator protein
MTBC0 PGAP re-annotationPucR family transcriptional regulator
Revised (this work)PucR family transcriptional regulator. Pfam: RsbRD_N (PF14361.13), GGDEF_2 (PF17853.7), HTH_30 (PF13556.13).

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

Curated reference (UniProt)

UniProt O06807 TrEMBL · unreviewed · Evidence at protein level
UniProt namePossible transcriptional activator protein

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category Q Secondary metabolites biosynthesis, transport and catabolism
T Signal transduction mechanisms
eggNOG descriptiontranscriptional
Orthologous groupCOG2508

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 0.454 · purifying
Polymorphic sites (≥ 0.1% of strains) 3 synonymous, 4 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
RsbRD_NPF14361.13 4.7e-0727–164 RsbT co-antagonist protein rsbRD N-terminal domain
GGDEF_2PF17853.7 1.1e-15187–295 GGDEF-like domain
HTH_30PF13556.13 9.0e-12344–396 PucR C-terminal helix-turn-helix domain

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

PartnerProductScoreNo text-miningChannels (≥400)
Rv3840 transcriptional regulator 839 839 coexpression:839
Rv3736 AraC/XylS family transcriptional regulator 833 833 coexpression:833
Rv3692 moxR2 methanol dehydrogenase transcriptional regulator MoxR 826 826 coexpression:826
Rv3124 moaR1 transcriptional regulator MoaR 824 824 coexpression:798
Rv1267c embR transcriptional regulator EmbR 824 824 coexpression:800
Rv1675c cmr HTH-type transcriptional regulator Cmr 817 817 coexpression:817
Rv0894 transcriptional regulator 811 812 coexpression:778
Rv3167c TetR family transcriptional regulator 805 805 coexpression:805
Rv1931c transcriptional regulator 802 802 coexpression:802
Rv1776c transcriptional regulator 802 802 coexpression:754
Rv2282c LysR family HTH-type transcriptional regulator 803 800 coexpression:800
Rv3263 DNA methylase 800 800 coexpression:800
Rv3183 higA3 transcriptional regulator 797 797 coexpression:797
Rv1167c transcriptional regulator 797 797 coexpression:797
Rv2488c LuxR family transcriptional regulator 797 797 coexpression:797

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: transcriptional activator protein
  • MTBC0 PGAP product: PucR family transcriptional regulator
  • Pfam (hmmscan --cut_ga): RsbRD_N PF14361.13 (E=5e-07), GGDEF_2 PF17853.7 (E=1e-15), HTH_30 PF13556.13 (E=9e-12)
  • (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_215969.2)
  • Domains: Pfam-A via hmmscan --cut_ga — RsbRD_N (PF14361.13), GGDEF_2 (PF17853.7), HTH_30 (PF13556.13)
  • 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 COG2508
  • Curated reference: UniProt O06807 (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 — 59 functional partner(s)
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001555|Rv1453|
MALRETSPRIHELIREAARIALNPTQEWLDEFDRAILAANPSIAADPALATVVKRSNRAHLIHFAAANLRNPGAPVPANLGPEPLRMARDLVRVGLDALALDIYRIGQNVAWRRWTDIAFGLTSDPDELHELLDVPFRTANEFVDTTLAGITTEMQLERDKLTRDVPAERRKIVQLLIDGAPISREHAEARLGYPLDRSHTAAVIWGDQAQGDHSHLDRVADAFGHAGGCPHPLVVVAGAATRWVWVKDAPGFDIDLIHEVLHDIPDARIAIGATAPGIEGFRRSHRDALTTARMIIRLESPHRVAFFTDVEMVALLTENAEGADDFIQRTLGNLESASPALKTTLLTFINQQCNASRAARLLFTHRNTLMNRLETAQRLLPRPLADTTIHVAVALEAQQWREKQTSDPPAKKESNGTKMR