yrbE1A Family assigned · medium auto-curated

H37Rv Rv0167 · MTBC0 mtbc0_000180 · 265 aa · 197209–198006 (+) · RefSeq NP_214681.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)membrane protein
MTBC0 PGAP re-annotationABC transporter permease
Revised (this work)ABC transporter permease. Pfam: MlaE (PF02405.22).

Auto-curated: this verdict and function were generated by rules from PGAP + Pfam + Foldseek and have not been hand-reviewed.

Curated reference (UniProt)

UniProt O07412 TrEMBL · unreviewed · Evidence at protein level
UniProt nameConserved integral membrane protein YrbE1A

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category Q Secondary metabolites biosynthesis, transport and catabolism
Preferred nameyrbE1A
eggNOG descriptionABC-type transport system involved in resistance to organic solvents, permease component
Orthologous groupCOG0767
KEGG orthology K02066
KEGG pathways map02010
KEGG modules M00210, M00669, M00670

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 0.098 · strong purifying
Polymorphic sites (≥ 0.1% of strains) 12 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)

PfamAccessioni-EvalueResiduesDescription
MlaEPF02405.22 7.6e-5747–256 Permease MlaE

Functional interaction network (STRING v12, guilt-by-association)

Closest characterised functional partner: mce1A (Mce family protein Mce1A), high confidence from genomic context alone (score 997 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv0169 mce1A Mce family protein Mce1A 999 997 ctx neighborhood:882 cooccurence:729 coexpression:881 textmining:811
Rv0170 mce1B Mce family protein Mce1B 998 997 ctx neighborhood:881 cooccurence:769 coexpression:874 textmining:581
Rv0171 mce1C Mce family protein Mce1C 998 997 ctx neighborhood:881 cooccurence:738 coexpression:881
Rv0174 mce1F Mce family protein Mce1F 999 996 ctx neighborhood:867 cooccurence:741 coexpression:849 textmining:909
Rv0655 mkl ABC transporter ATP-binding protein 997 996 ctx cooccurence:773 coexpression:846 experimental:505 database:800 textmining:469
Rv0172 mce1D Mce family protein Mce1D 997 995 ctx neighborhood:792 cooccurence:753 coexpression:871 textmining:467
Rv0173 lprK Mce family lipoprotein LprK 997 994 ctx neighborhood:786 cooccurence:759 coexpression:853 textmining:606
Rv0168 yrbE1B membrane protein 989 982 ctx neighborhood:800 coexpression:819 textmining:432
Rv0166 fadD5 fatty-acid--CoA ligase FadD5 963 897 ctx neighborhood:474 coexpression:813 textmining:659
Rv3497c mce4C Mce family protein Mce4C 881 879 ctx cooccurence:770
Rv0592 mce2D Mce family protein Mce2D 881 874 ctx cooccurence:763
Rv3496c mce4D Mce family protein Mce4D 879 872 ctx cooccurence:766
Rv3498c mce4B Mce family protein Mce4B 877 872 ctx cooccurence:770
Rv0590 mce2B Mce-family protein Mce2B; Rv0590, (MTCY19H5.32c), len: 275 aa. Mce2B; belongs to 24-membered Mycobacterium tuberculosis Mce protein family ( 884 871 ctx cooccurence:769
Rv1971 mce3F Mce family protein Mce3F 873 871 ctx cooccurence:765

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: membrane protein
  • MTBC0 PGAP product: ABC transporter permease
  • Pfam (hmmscan --cut_ga): MlaE PF02405.22 (E=8e-57)
  • (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_214681.1)
  • Domains: Pfam-A via hmmscan --cut_ga — MlaE (PF02405.22)
  • 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 COG0767
  • Curated reference: UniProt O07412 (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 — 51 functional partner(s); context anchor mce1A
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_000180|Rv0167|yrbE1A
MTTSTTLGGYVRDQLQTPLTLVGGFFRMCVLTGKALFRWPFQWREFILQCWFIMRVGFLPTIMVSIPLTVLLIFTLNILLAQFGAADISGSGAAIGAVTQLGPLTTVLVVAGAGSTAICADLGARTIREEIDAMEVLGIDPIHRLVVPRVLASMLVATLLNGLVITVGLVGGFLFGVYLQNVSGGAYLATLTLITGLPEVVIATIKAATFGLIAGLVGCYRGLTVRGGSKGLGTAVNETVVLCVIALFAVNVILTTIGVRFGTGR