Rv1590 Family assigned · medium auto-curated

H37Rv Rv1590 · MTBC0 mtbc0_001696 · 79 aa · 1803298–1803537 (+) · RefSeq NP_216106.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)hypothetical protein
MTBC0 PGAP re-annotationhypothetical protein
Revised (this work)Contains BsaP (PF26519.1) 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 P9WLT7 SwissProt · reviewed · Evidence at protein level
UniProt nameBiotin synthase auxiliary protein
Curated functionRequired for the activity of the biotin synthase BioB.

Functional vocabulary (eggNOG-mapper, orthology transfer)

Orthologous group2EH0W
Gene Ontology (33) GO:0002682, GO:0002684, GO:0008150, GO:0009605, GO:0009607, GO:0035821, GO:0043207, GO:0044003, GO:0044403, GO:0044419, GO:0048518, GO:0048583 +21 more

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)

PfamAccessioni-EvalueResiduesDescription
BsaPPF26519.1 5.7e-1751–79 Biotin synthase auxiliary protein family

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

Closest characterised functional partner: bioB (biotin synthetase), high confidence from genomic context alone (score 956 excluding text-mining). This association is the citable seed of a function hypothesis for this hypothetical protein.

PartnerProductScoreNo text-miningChannels (≥400)
Rv1589 bioB biotin synthetase 959 956 ctx neighborhood:881 cooccurence:556
Rv1591 transmembrane protein 887 887 ctx neighborhood:881
Rv1343c lprD lipoprotein LprD 663 663 ctx cooccurence:662
Rv2001 hyp hypothetical protein 550 551 ctx cooccurence:548
Rv2418c octT hyp hypothetical protein 519 520 ctx cooccurence:508
Rv2609c membrane protein 504 505 ctx cooccurence:493
Rv2673 aftC alpha-(1->3)-arabinofuranosyltransferase 502 503 ctx cooccurence:496
Rv1570 bioD ATP-dependent dethiobiotin synthetase BioD 521 500
Rv1683 bifunctional long-chain acyl-CoA synthase/lipase 494 495 ctx cooccurence:480
Rv3805c aftB terminal beta-(1->2)-arabinofuranosyltransferase 482 482 ctx cooccurence:479
Rv0464c hyp hypothetical protein 481 482 ctx cooccurence:477
Rv3755c hyp hypothetical protein 479 480 ctx cooccurence:478
Rv0876c transmembrane protein 460 461 ctx cooccurence:459
Rv3802c membrane protein 430 431 ctx cooccurence:428
Rv2739c transferase 430 431 ctx cooccurence:424

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): BsaP PF26519.1 (E=6e-17)
  • (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_216106.1)
  • Domains: Pfam-A via hmmscan --cut_ga — BsaP (PF26519.1)
  • 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 2EH0W
  • Curated reference: UniProt P9WLT7 (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 — 20 functional partner(s); context anchor bioB
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001696|Rv1590|
MVEIVAGKQRAPVAAGVYNVYTGELADTATPTAARMGLEPPRFCAQCGRRMVVQVRPDGWWARCSRHGQVDSADLATQR