Rv2075c Family assigned · medium auto-curated
H37Rv Rv2075c · MTBC0 mtbc0_002209 ·
487 aa · 2360029–2361492 (-) ·
RefSeq NP_216591.1
Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | hypothetical protein |
|---|---|
| MTBC0 PGAP re-annotation | hypothetical protein |
| Revised (this work) | Contains PI-PLC_cat (PF26178.1) domain(s); putative function inferred from the domain architecture. |
Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.
Curated reference (UniProt)
| UniProt |
P9WLL5
SwissProt · reviewed
· Predicted
|
|---|---|
| UniProt name | Uncharacterized protein Rv2075c |
UniProt still lists this protein as Uncharacterized protein Rv2075c; the revised annotation above is ahead of the current UniProt record.
Functional vocabulary (eggNOG-mapper, orthology transfer)
| Orthologous group | 2E3JJ |
|---|
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 | 3.953 · diversifying/relaxed |
|---|---|
| Polymorphic sites (≥ 0.1% of strains) | 1 synonymous, 11 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 |
|---|---|---|---|---|
PI-PLC_cat | PF26178.1 | 2.1e-06 | 112–235 | PI-PLC-like catalytic domain |
Functional interaction network (STRING v12, guilt-by-association)
Closest characterised functional partner: PE_PGRS28 (PE-PGRS family protein PE_PGRS28), high confidence from genomic context alone (score 737 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) |
|---|---|---|---|---|
Rv1452c PE_PGRS28 |
PE-PGRS family protein PE_PGRS28 | 737 | 737 ctx | cooccurence:737 |
Rv1004c |
membrane protein | 722 | 723 ctx | cooccurence:719 |
Rv2490c PE_PGRS43 |
PE-PGRS family protein PE_PGRS43 | 721 | 721 ctx | cooccurence:721 |
Rv2209 |
integral membrane protein | 719 | 719 ctx | cooccurence:718 |
Rv0355c PPE8 |
PPE family protein PPE8 | 716 | 717 ctx | cooccurence:715 |
Rv0341 iniB |
isoniazid inducible protein IniB | 716 | 716 ctx | cooccurence:714 |
Rv3347c PPE55 |
PPE family protein PPE55 | 712 | 713 ctx | cooccurence:711 |
Rv3350c PPE56 |
PPE family protein PPE56 | 712 | 712 ctx | cooccurence:711 |
Rv3879c espK |
ESX-1 secretion-associated protein EspK | 691 | 691 ctx | cooccurence:691 |
Rv0104 hyp |
hypothetical protein | 688 | 689 ctx | cooccurence:683 |
Rv1651c PE_PGRS30 |
PE-PGRS family protein PE_PGRS30 | 684 | 684 ctx | cooccurence:684 |
Rv0304c PPE5 |
PPE family protein PPE5 | 674 | 674 ctx | cooccurence:672 |
Rv1917c PPE34 |
PPE family protein PPE34 | 668 | 669 ctx | cooccurence:667 |
Rv3343c PPE54 |
PPE family protein PPE54 | 667 | 667 ctx | cooccurence:666 |
Rv2819c csm5 |
CRISPR type III-associated RAMP protein Csm5 | 662 | 662 ctx | cooccurence:661 |
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
- Pfam (hmmscan --cut_ga): PI-PLC_cat PF26178.1 (E=2e-06)
- (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_216591.1)
- Domains: Pfam-A via hmmscan --cut_ga — PI-PLC_cat (PF26178.1)
- 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
2E3JJ - Curated reference: UniProt P9WLL5 (SwissProt, reviewed; 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)
- Interaction network: STRING v12.0 (Szklarczyk et al. 2023,
doi:10.1093/nar/gkac1000), taxon 83332, CC-BY 4.0 —
87 functional partner(s); context anchor
PE_PGRS28 - Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_002209|Rv2075c| MPRARWLQSAALMGALAVVLITAAPVAADAYQVPAPPSPTASCDVISPVAIPCVALGKFADAVAAECRRVGVPDARCVLPLAHRVTQAARDAYLQSWVHRTARFQDALQDPVPLRETQWLGTHNSFNSLSDSFTVSHADSNQQLSLAQQLDIDVRALELDLHYLPRLEGHGAPGVTVCHGLGPKNANLGCTVEPLLATVLPQIANWLNAPGHTEEVILLYLEDQLKNASAYESVVATLDQVLRRADGTSLIYRPNPARRATNGCVPLPLDVSREEIRASGARAVLVGSCAPGWSAAVFDWSGVELESGSNSGYRPYPACDATYGRGVYAWRLVRYYEDSTLATALANPTRPPANPQALTPPKVQAMTDCGVNLFGFDQLLPEDGRIQASLWSWAPDEPRAGAGACALQGADGRWVAASCGDPHPAACRDAAGRWTVTPAPVVFAGAALACTAIGADFTLPRTGNQNARLHAVAGPAGGAWVHYLLPP