Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | transcriptional regulator |
| MTBC0 PGAP re-annotation | helix-turn-helix domain-containing protein |
| Revised (this work) | Helix-turn-helix domain-containing protein. Pfam: HTH_17 (PF12728.14). |
Auto-curated: this verdict and function were generated by rules from
PGAP + Pfam + Foldseek and have not been hand-reviewed.
Curated reference (UniProt)
| UniProt |
O53807
TrEMBL · unreviewed
· Evidence at protein level
|
| UniProt name | Possible transcriptional regulatory protein |
Functional vocabulary (eggNOG-mapper, orthology transfer)
| COG category |
K Transcription
|
| eggNOG description | Helix-turn-helix domain |
| Orthologous group | 2C22B |
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 |
0.631 · 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)
| Pfam | Accession | i-Evalue | Residues | Description |
HTH_17 | PF12728.14 |
5.4e-11 | 4–49 |
Helix-turn-helix domain |
Functional interaction network (STRING v12, guilt-by-association)
| Partner | Product | Score | No text-mining | Channels (≥400) |
Rv0743c hyp |
hypothetical protein |
883 |
882 ctx |
neighborhood:882 |
Rv1776c |
transcriptional regulator |
800 |
800 |
coexpression:800 |
Rv3167c |
TetR family transcriptional regulator |
799 |
799 |
coexpression:799 |
Rv1151c cobB |
NAD-dependent protein deacylase |
797 |
797 |
coexpression:797 |
Rv3830c |
TetR family transcriptional regulator |
797 |
797 |
coexpression:797 |
Rv0603 hyp |
hypothetical protein |
797 |
797 |
coexpression:797 |
Rv1985c lysG |
HTH-type transcriptional regulator |
767 |
767 |
coexpression:767 |
Rv0602c tcrA |
two component DNA binding transcriptional regulator TcrA |
767 |
767 |
coexpression:767 |
Rv1267c embR |
transcriptional regulator EmbR |
759 |
759 |
coexpression:759 |
Rv1675c cmr |
HTH-type transcriptional regulator Cmr |
744 |
744 |
coexpression:744 |
Rv1167c |
transcriptional regulator |
744 |
744 |
coexpression:744 |
Rv3736 |
AraC/XylS family transcriptional regulator |
733 |
733 |
coexpression:733 |
Rv1960c parD1 |
antitoxin ParD1 |
733 |
733 |
coexpression:733 |
Rv0691c mftR |
mycofactocin biosynthesis transcriptional regulator MftR |
733 |
733 |
coexpression:733 |
Rv3840 |
transcriptional regulator |
732 |
732 |
coexpression:732 |
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 regulator
- MTBC0 PGAP product: helix-turn-helix domain-containing protein
- Pfam (hmmscan --cut_ga): HTH_17 PF12728.14 (E=5e-11)
- (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_215258.1)
- Domains: Pfam-A via hmmscan --cut_ga — HTH_17 (PF12728.14)
- 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
2C22B
- Curated reference: UniProt
O53807
(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 —
38 functional partner(s)
- Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_000789|Rv0744c|
METLLKTSEAAQILGVSRQHVVNMCDRGEMVCVHVGSHRRVPSSEVERVTSRRLTREEERSLWLHRALLSPLLTEPDTVVSAARENLRRWSGMHRRDGMAGWYFTKWQRVLNDGLDAVMHVLTSPSEDAREMRQNSPFAGILPEATRVAVLRSFKDHWDREHERAMTE
Spot an error? Suggest an improvement