Rv2432c Still unknown · low auto-curated
H37Rv Rv2432c · MTBC0 mtbc0_002590 ·
136 aa · 2752685–2753095 (-) ·
RefSeq NP_216948.1
Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | hypothetical protein |
|---|---|
| MTBC0 PGAP re-annotation | hypothetical protein |
| Revised (this work) | Conserved hypothetical protein; no recognised domain. Function unknown. Foldseek best (non-significant) hit: 3e90-assembly3_C West Nile vi rus NS2B-NS3protease in complexed with i (prob 0.03, TM 0.44). |
Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.
Curated reference (UniProt)
| UniProt |
P71917
TrEMBL · unreviewed
· Predicted
|
|---|---|
| UniProt name | Uncharacterized protein |
UniProt still lists this protein as Uncharacterized protein; the revised annotation above is ahead of the current UniProt record.
Conservation & selection (intra-MTBC, 145 209 strains)
| pN/pS | n/a |
|---|---|
| Polymorphic sites (≥ 0.1% of strains) | 0 synonymous, 1 missense, 0 nonsense, 1 frameshift |
| Disruption | 1 distinct premature-stop/frameshift site(s); most common in 0.12% of strains (179) · 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)
No Pfam-A domain above the gathering threshold (or not yet scanned).
Structural neighbours (Foldseek on the ESMFold model, exploratory)
ESMFold model confidence: mean pLDDT 29.9 (very low). Low-confidence model: the fold may be unreliable, so treat these structural hits with caution.
Best matches against the PDB, ranked by Foldseek homology probability. A high probability / TM-score suggests a shared fold; unless flagged sig (E < 0.01) these are fold hypotheses, not assignments.
| Target | Prob | TM | E-value | Description |
|---|---|---|---|---|
3e90-assembly3_C |
0.03 | 0.44 | 9.6e+00 | 3e90-assembly3_C West Nile vi rus NS2B-NS3protease in complexed with inhibitor Naph-KKR-H |
7vxx-assembly2_C |
0.02 | 0.36 | 7.9e+00 | 7vxx-assembly2_C Zika virus NS2B/NS3 protease bZipro(C143S) in complex with 4-amino benzamidine |
5h6v-assembly1_A |
0.02 | 0.36 | 7.9e+00 | 5h6v-assembly1_A Structure of Zika virus protease in complex with a dipeptide inhibitor |
7am2-assembly1_BB |
0.01 | 0.21 | 7.0e+00 | 7am2-assembly1_BB Intermediate assembly of the Large subunit from Leishmania major mitochondrial ribosome |
7ane-assembly1_BB |
0.01 | 0.19 | 7.5e+00 | 7ane-assembly1_BB Leishmania Major mitochondrial ribosome |
Functional interaction network (STRING v12, guilt-by-association)
Closest characterised functional partner: Rv2434c (transmembrane protein), high confidence from genomic context alone (score 887 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.
| Partner | Product | Score | No text-mining | Channels (≥400) |
|---|---|---|---|---|
Rv2433c nrtS hyp |
hypothetical protein | 907 | 907 ctx | neighborhood:882 |
Rv2434c |
transmembrane protein | 887 | 887 ctx | neighborhood:882 |
Rv2435c |
cyclase | 804 | 804 ctx | neighborhood:801 |
Rv2431c PE25 |
PE family protein PE25 | 492 | 492 ctx | neighborhood:492 |
Rv2430c PPE41 |
PPE family protein PPE41 | 417 | 417 ctx | neighborhood:408 |
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: hypothetical protein
- MTBC0 PGAP product: hypothetical protein
- Foldseek best: 3e90-assembly3_C West Nile vi rus NS2B-NS3protease in complexed with inhibitor N (prob 0.03, E=1e+01, TM=0.44)
- (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_216948.1)
- Domains: Pfam-A via hmmscan --cut_ga — none above threshold
- Sequence-level signal: ESM Atlas (EvolutionaryScale × BioHub) — exploratory
- Curated reference: UniProt P71917 (TrEMBL, unreviewed; Predicted)
- Intra-MTBC selection: pN/pS and disruption from SPDI variants of 145 209 MTBC strains (this work, local collection vs H37Rv NC_000962.3)
- Model confidence: ESMFold per-residue pLDDT (mean 29.9, very low)
- Interaction network: STRING v12.0 (Szklarczyk et al. 2023,
doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 —
5 functional partner(s); context anchor
Rv2434c - Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_002590|Rv2432c| MTVRAEHCRGAGGCDECPSVMPEHPTALFHDVAAIALAQPGAEPGAMMGFPCRPALLPHLSRAVMRCVRTRSASTSLGVSVIAGQLPAAGSRHRLGAPCRHVRWWLASDGHWGMVSYIPTALNVSMGGIVGWRCVP