Rv1816 Family assigned · medium auto-curated

H37Rv Rv1816 · MTBC0 - · 234 aa · 2058256–2058960 (+) · RefSeq NP_216332.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)HTH-type transcriptional regulator
MTBC0 PGAP re-annotation
Revised (this work)HTH-type transcriptional regulator. Pfam: TetR_N (PF00440.30), TetR_C_33 (PF13305.12).

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 P9WMC9 SwissProt · reviewed · Evidence at protein level
UniProt nameHTH-type transcriptional regulator Rv1816
Curated functionMay participate in the regulatory network that controls the expression of MmpL lipid transporters. Binds to intragenic and/or promoter regions of rv1816, mmpL3, rv0204, mmpL11, mmpL7, kasA and mmpS3.

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category K Transcription
eggNOG descriptiontetR family
Orthologous groupCOG1309
Gene Ontology (22) GO:0003674, GO:0003700, GO:0006355, GO:0008150, GO:0009889, GO:0010468, GO:0010556, GO:0019219, GO:0019222, GO:0031323, GO:0031326, GO:0050789 +10 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) pseudogene candidate

pN/pS 0.698 · relaxed/neutral
Polymorphic sites (≥ 0.1% of strains) 2 synonymous, 4 missense, 0 nonsense, 2 frameshift
Disruption 2 distinct premature-stop/frameshift site(s); most common in 5.77% of strains (8384) · clonal

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
TetR_NPF00440.30 1.7e-0621–64 Bacterial regulatory proteins, tetR family
TetR_C_33PF13305.12 4.2e-2196–225 Tetracyclin repressor-like, C-terminal domain

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

Closest characterised functional partner: eccD2 (ESX-2 secretion system protein EccD), medium confidence from genomic context alone (score 559 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1815 hyp hypothetical protein 938 938 ctx neighborhood:700 coexpression:802
Rv2423 hyp hypothetical protein 606 606 ctx cooccurence:606
Rv3899c hyp hypothetical protein 590 590 ctx cooccurence:586
Rv2067c hyp hypothetical protein 565 566 ctx cooccurence:560
Rv3887c eccD2 ESX-2 secretion system protein EccD 558 559 ctx cooccurence:556
Rv1817 flavoprotein 546 546 ctx neighborhood:544
Rv0736 rslA anti-sigma-L factor RslA 531 531 ctx cooccurence:523
Rv3435c transmembrane protein 487 488 ctx cooccurence:480
Rv1748 hyp hypothetical protein 482 482 ctx cooccurence:482
Rv1814 erg3 membrane-bound C-5 sterol desaturase 475 475 ctx neighborhood:475
Rv1014c pth peptidyl-tRNA hydrolase 404 404 coexpression:402
Rv0827c kmtR HTH-type transcriptional regulator KmtR 521 56 textmining:514
Rv1423 whiA transcriptional regulator WhiA 662 55 textmining:657
Rv3246c mtrA two component DNA-binding response regulator MtrA 552 55 textmining:546
Rv1828 HTH-type transcriptional regulator 813 53 textmining:811

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): HTH-type transcriptional regulator
  • Pfam (hmmscan --cut_ga): TetR_N PF00440.30 (E=2e-06), TetR_C_33 PF13305.12 (E=4e-21)
  • (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_216332.1)
  • Domains: Pfam-A via hmmscan --cut_ga — TetR_N (PF00440.30), TetR_C_33 (PF13305.12)
  • 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 COG1309
  • Curated reference: UniProt P9WMC9 (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 — 20 functional partner(s); context anchor eccD2
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>H37Rv|Rv1816|
MCQTCRVGKRRDAREQIEAKIVELGRRQLLDHGAAGLSLRAIARNLGMVSSAVYRYVSSRDELLTLLLVDAYSDLADTVDRARDDTVADSWSDDVIAIARAVRGWAVTNPARWALLYGSPVPGYHAPPDRTAGVATRVVGAFFDAIAAGIATGDIRLTDDVAPQPMSSDFEKIRQEFGFPGDDRVVTKCFLLWAGVVGAISLEVFGQYGADMLTDPGVVFDAQTRLLVAVLAEH