rfbE Family assigned · medium auto-curated
H37Rv Rv3781 · MTBC0 mtbc0_004009 ·
273 aa · 4251650–4252471 (+) ·
RefSeq NP_218298.1
Annotation: from legacy to revised
| Legacy (H37Rv / Mycobrowser) | O-antigen/lipopolysaccharide ABC transporter ATP-binding protein RfbE |
|---|---|
| MTBC0 PGAP re-annotation | ABC transporter ATP-binding protein |
| Revised (this work) | ABC transporter ATP-binding protein. Pfam: ABC_tran (PF00005.34). |
Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.
Curated reference (UniProt)
| UniProt |
P72047
TrEMBL · unreviewed
· Evidence at protein level
|
|---|---|
| UniProt name | Probable O-antigen/lipopolysaccharide transport ATP-binding protein ABC transporter RfbE |
Functional vocabulary (eggNOG-mapper, orthology transfer)
| COG category |
G Carbohydrate transport and metabolismM Cell wall / membrane / envelope biogenesis
|
|---|---|
| Preferred name | rfbE |
| eggNOG description | ABC transporter |
| Orthologous group | COG1134 |
| KEGG orthology |
K01990, K09691
|
| KEGG pathways |
map02010
|
| KEGG modules |
M00250, M00254
|
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 | 0.0 · strong purifying |
|---|---|
| Polymorphic sites (≥ 0.1% of strains) | 1 synonymous, 0 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 |
|---|---|---|---|---|
ABC_tran | PF00005.34 | 2.6e-19 | 53–183 | ABC transporter |
Functional interaction network (STRING v12, guilt-by-association)
Closest characterised functional partner: rfbD (O-antigen/lipopolysaccharide ABC transporter permease RfbD), high confidence from genomic context alone (score 1000 excluding text-mining).
| Partner | Product | Score | No text-mining | Channels (≥400) |
|---|---|---|---|---|
Rv3783 rfbD |
O-antigen/lipopolysaccharide ABC transporter permease RfbD | 999 | 1000 ctx | neighborhood:881 cooccurence:772 coexpression:864 experimental:928 database:900 textmining:917 |
Rv3782 glfT1 |
galactofuranosyl transferase GlfT | 992 | 939 ctx | neighborhood:882 textmining:879 |
Rv3780 bpa hyp |
hypothetical protein | 964 | 884 ctx | neighborhood:882 textmining:703 |
Rv3779 |
transmembrane protein | 930 | 882 ctx | neighborhood:881 textmining:434 |
Rv3242c hyp |
hypothetical protein | 776 | 777 | coexpression:777 |
Rv2894c xerC |
tyrosine recombinase XerC | 646 | 646 | coexpression:646 |
Rv3265c wbbL1 |
N-acetylglucosaminyl-diphospho-decaprenol L-rhamnosyltransferase | 880 | 643 ctx | cooccurence:402 textmining:678 |
Rv3778c |
aminotransferase | 637 | 637 ctx | neighborhood:636 |
Rv3809c glf |
UDP-galactopyranose mutase | 791 | 557 | coexpression:415 textmining:549 |
Rv3784 |
dTDP-glucose 4,6-dehydratase | 569 | 518 ctx | neighborhood:511 |
Rv2584c apt |
adenine phosphoribosyltransferase | 495 | 495 | coexpression:479 |
Rv3754 tyrA |
prephenate dehydrogenase TyrA | 507 | 489 | coexpression:419 |
Rv3226c hyp |
hypothetical protein | 469 | 470 | |
Rv3786c hyp |
hypothetical protein | 496 | 469 | coexpression:451 |
Rv1502 hyp |
hypothetical protein | 475 | 456 | coexpression:425 |
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: O-antigen/lipopolysaccharide ABC transporter ATP-binding protein RfbE
- MTBC0 PGAP product: ABC transporter ATP-binding protein
- Pfam (hmmscan --cut_ga): ABC_tran PF00005.34 (E=3e-19)
- (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_218298.1)
- Domains: Pfam-A via hmmscan --cut_ga — ABC_tran (PF00005.34)
- 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
COG1134 - Curated reference: UniProt P72047 (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 —
37 functional partner(s); context anchor
rfbD - Primary literature: none located yet; annotation rests on the domain/homology sources above.
Ancestral MTBC0 protein sequence
>mtbc0_004009|Rv3781|rfbE MSDPHHPHIQTHNAWVEFPIFDAKSRSLKKAVLGKAGGTIGRNNSNVVVIEALRDITMELNLGDRVGLVGHNGAGKSTLLRLLSGIYEPTRGWAKVTGRVAPVFDLGIGMDPEISGYENIIIRGLFLGQTRKQMQAKVDEIAEFTELGEYLSMPLRTYSTGMRVRLAMGVVTSIDPEILLLDEGIGAVDADFLRKAQSRLQNLVERSGILVFASHSNEFLARLCKTAIWIDHGVIRLAGGIEEVVRAYEGEDAARHVREVLAETQADRQNVQG