Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | hypothetical protein |
| MTBC0 PGAP re-annotation | LpqN/LpqT family lipoprotein |
| Revised (this work) | Cell-envelope lipoprotein of the LpqN/LpqT family (Pfam Lpp-LpqN, PF10738). Members are anchored to the mycobacterial envelope; the specific physiological role of this locus is not established here. |
Curated reference (UniProt)
| UniProt |
P9WIM9
SwissProt · reviewed
· Evidence at protein level
|
| UniProt name | Proline-rich 28 kDa antigen |
Functional vocabulary (eggNOG-mapper, orthology transfer)
| COG category |
S Function unknown
|
| Preferred name | mtc28 |
| eggNOG description | Probable lipoprotein LpqN |
| Orthologous group | 2APGE |
| Gene Ontology (2) |
GO:0005575, GO:0005576
|
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 |
1.001 · relaxed/neutral
|
| Polymorphic sites (≥ 0.1% of strains) |
3 synonymous, 8 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 |
Lpp-LpqN | PF10738.16 |
1.5e-66 | 103–270 |
Probable lipoprotein LpqN |
Functional interaction network (STRING v12, guilt-by-association)
Closest characterised functional partner:
Rv0039c (transmembrane protein),
high confidence from genomic context alone
(score 794 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) |
Rv3810 pirG |
cell surface protein |
812 |
812 |
coexpression:812 |
Rv0312 hyp |
hypothetical protein |
812 |
812 |
coexpression:812 |
Rv2721c hyp |
hypothetical protein |
803 |
803 |
coexpression:803 |
Rv1477 ripA |
peptidoglycan endopeptidase RipA |
810 |
800 |
coexpression:800 |
Rv0039c |
transmembrane protein |
794 |
794 ctx |
neighborhood:785 |
Rv1158c hyp |
hypothetical protein |
748 |
748 |
coexpression:748 |
Rv1478 ripB |
peptidoglycan endopeptidase RipB |
738 |
738 |
coexpression:738 |
Rv1566c ripD hyp |
hypothetical protein |
747 |
734 |
coexpression:734 |
Rv0041 leuS |
leucine--tRNA ligase |
731 |
732 ctx |
neighborhood:730 |
Rv0888 spmT hyp |
hypothetical protein |
703 |
703 |
coexpression:703 |
Rv1157c hyp |
hypothetical protein |
414 |
415 |
coexpression:415 |
Rv1754c hyp |
hypothetical protein |
415 |
386 |
|
Rv1926c mpt63 |
immunogenic protein Mpt63 |
547 |
46 |
textmining:545 |
Rv3279c birA |
bifunctional biotin operon repressor/biotin--[acetyl-CoA-carboxylase |
659 |
44 |
textmining:658 |
Rv3221c TB7.3 |
acetyl-CoA carboxylase biotin carboxyl carrier protein subunit |
808 |
42 |
textmining:808 |
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
- MTBC0 PGAP product: 'LpqN/LpqT family lipoprotein'
- Pfam (hmmscan --cut_ga): Lpp-LpqN PF10738 (E=1.5e-66)
ESM Atlas signal (exploratory)
Ancestral protein hash 1f4cb89e38667edbbb0f4d2ccec8f10a.
SAE features are orienting indices, not validated domains.
| # | Index | Activation | Interpretation |
| 1 | 3621 |
1.17 |
Secretory pathway signal motifs |
| 2 | 11966 |
1.16 |
Low-cysteine small/charged soluble tracts |
| 3 | 15441 |
1.13 |
Catalysis-adjacent beta-strand micro-motifs |
| 4 | 6474 |
1.12 |
Acidic/disulfide loops and catalytic Asp/His |
| 5 | 777 |
1.11 |
N-terminal targeting signals |
| 6 | 1070 |
0.89 |
Exposed amphipathic alpha helices |
| 7 | 7087 |
0.70 |
Extracellular low-complexity repeats |
| 8 | 13555 |
0.68 |
Small-residue low-complexity tracts |
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_214554.2)
- Domains: Pfam-A via hmmscan --cut_ga — Lpp-LpqN (PF10738.16)
- 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
2APGE
- Curated reference: UniProt
P9WIM9
(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 —
15 functional partner(s); context anchor
Rv0039c
- Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_000045|Rv0040c|mtc28
MIQIARTWRVFAGGMATGFIGVVLVTAGKASADPLLPPPPIPAPVSAPATVPPVQNLTALPGGSSNRFSPAPAPAPIASPIPVGAPGSTAVPPLPPPVTPAISGTLRDHLREKGVKLEAQRPHGFKALDITLPMPPRWTQVPDPNVPDAFVVIADRLGNSVYTSNAQLVVYRLIGDFDPAEAITHGYIDSQKLLAWQTTNASMANFDGFPSSIIEGTYRENDMTLNTSRRHVIATSGADKYLVSLSVTTALSQAVTDGPATDAIVNGFQVVAHAAPAQAPAPAPGSAPVGLPGQAPGYPPAGTLTPVPPR
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