Rv1669 Still unknown · low auto-curated
H37Rv Rv1669 · MTBC0 mtbc0_001776 ·
120 aa · 1907740–1908102 (+) ·
RefSeq NP_216185.1
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: 3jsy-assembly2_B N-terminal fragment of ribosomal protein L10 from Met (prob 0.10, TM 0.55). |
Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.
Curated reference (UniProt)
| UniProt |
O86371
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 | 1.043 · relaxed/neutral |
|---|---|
| Polymorphic sites (≥ 0.1% of strains) | 1 synonymous, 3 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)
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 34.7 (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 |
|---|---|---|---|---|
3jsy-assembly2_B |
0.10 | 0.55 | 5.1e+00 | 3jsy-assembly2_B N-terminal fragment of ribosomal protein L10 from Methanococcus jannaschii |
1p91-assembly1_B |
0.09 | 0.44 | 2.1e+00 | 1p91-assembly1_B Crystal Structure of RlmA(I) enzyme: 23S rRNA n1-G745 methyltransferase (NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ER19) |
8ipd-assembly1_v |
0.08 | 0.47 | 3.5e+00 | 8ipd-assembly1_v human nuclear pre-60S ribosomal particle - State C |
7ohp-assembly1_W |
0.07 | 0.44 | 4.0e+00 | 7ohp-assembly1_W Nog1-TAP associated immature ribosomal particles from S. cerevisiae after rpL25 expression shut down, population A |
3r5c-assembly1_A |
0.07 | 0.57 | 8.9e+00 | 3r5c-assembly1_A Pseudomonas aeruginosa DapD (PA3666) in complex with CoA and succinate |
1p91-assembly1_A |
0.06 | 0.35 | 2.0e+00 | 1p91-assembly1_A Crystal Structure of RlmA(I) enzyme: 23S rRNA n1-G745 methyltransferase (NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ER19) |
3r5a-assembly2_F |
0.06 | 0.48 | 6.5e+00 | 3r5a-assembly2_F Pseudomonas aeruginosa DapD (PA3666) in complex with D-2-aminopimelate |
3r5c-assembly1_C |
0.06 | 0.53 | 8.4e+00 | 3r5c-assembly1_C Pseudomonas aeruginosa DapD (PA3666) in complex with CoA and succinate |
Functional interaction network (STRING v12, guilt-by-association)
Closest characterised functional partner: Rv1671 (membrane protein), high confidence from genomic context alone (score 715 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) |
|---|---|---|---|---|
Rv1671 |
membrane protein | 715 | 715 ctx | neighborhood:712 |
Rv1670 hyp |
hypothetical protein | 712 | 712 ctx | neighborhood:712 |
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: 3jsy-assembly2_B N-terminal fragment of ribosomal protein L10 from Methanococcus (prob 0.10, E=5e+00, TM=0.55)
- (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_216185.1)
- Domains: Pfam-A via hmmscan --cut_ga — none above threshold
- Sequence-level signal: ESM Atlas (EvolutionaryScale × BioHub) — exploratory
- Curated reference: UniProt O86371 (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 34.7, very low)
- Interaction network: STRING v12.0 (Szklarczyk et al. 2023,
doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 —
2 functional partner(s); context anchor
Rv1671 - Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_001776|Rv1669| MSRRPGYSNGRAGASRQAARGGSAGASSVAFSSQPNCGLTESVLGHQVTGICLGTIHLDAMQWPWSSAYRLEPAVATTLIGISAWWANGSVKQYAGDLTDRVATMTVCRRTPAPRVHYRQ