Rv1683 Resolved · high auto-curated

H37Rv Rv1683 · MTBC0 mtbc0_001791 · 999 aa · 1919609–1922608 (+) · RefSeq NP_216199.1

Annotation: from legacy to revised

Legacy (H37Rv / Mycobrowser)bifunctional long-chain acyl-CoA synthase/lipase
MTBC0 PGAP re-annotationacyl-CoA synthetase
Revised (this work)Acyl-CoA synthetase. Pfam: Abhydrolase_1 (PF00561.27), AMP-binding (PF00501.35).

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

Curated reference (UniProt)

UniProt O33185 TrEMBL · unreviewed · Evidence at protein level
UniProt namePossible bifunctional enzyme long-chain acyl-CoA synthase and lipase

Functional vocabulary (eggNOG-mapper, orthology transfer)

COG category I Lipid transport and metabolism
Q Secondary metabolites biosynthesis, transport and catabolism
eggNOG descriptionsynthetase
Orthologous groupCOG0318
KEGG orthology K03821, K03822
KEGG pathways map00650

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 0.35 · purifying
Polymorphic sites (≥ 0.1% of strains) 8 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)

PfamAccessioni-EvalueResiduesDescription
Abhydrolase_1PF00561.27 3.7e-07100–342 alpha/beta hydrolase fold
AMP-bindingPF00501.35 4.4e-28455–783 AMP-binding enzyme

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

Closest characterised functional partner: Rv2876 (transmembrane protein), medium confidence from genomic context alone (score 639 excluding text-mining).

PartnerProductScoreNo text-miningChannels (≥400)
Rv1684 hyp hypothetical protein 918 918 ctx neighborhood:881
Rv2933 ppsC phthiocerol synthesis polyketide synthase type I PpsC 776 705
Rv2940c mas multifunctional mycocerosic acid synthase 776 705
Rv1527c pks5 polyketide synthase 775 704
Rv2048c pks12 polyketide synthase 775 704
Rv3825c pks2 phthioceranic/hydroxyphthioceranic acid synthase 775 704
Rv0719 rplF 50S ribosomal protein L6 696 696 experimental:402 database:510
Rv1125 hyp hypothetical protein 675 673 ctx cooccurence:550
Rv0464c hyp hypothetical protein 696 671 ctx cooccurence:662
Rv3807c decaprenylphosphoryl-5-phosphoribose phosphatase 672 659 database:500
Rv3800c pks13 polyketide synthase 680 640
Rv2876 transmembrane protein 639 639 ctx cooccurence:636
Rv2946c pks1 polyketide synthase 675 635
Rv0756c hyp hypothetical protein 621 621 ctx cooccurence:621
Rv1181 pks4 polyketide beta-ketoacyl synthase 637 614

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: bifunctional long-chain acyl-CoA synthase/lipase
  • MTBC0 PGAP product: acyl-CoA synthetase
  • Pfam (hmmscan --cut_ga): Abhydrolase_1 PF00561.27 (E=4e-07), AMP-binding PF00501.35 (E=4e-28)
  • (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_216199.1)
  • Domains: Pfam-A via hmmscan --cut_ga — Abhydrolase_1 (PF00561.27), AMP-binding (PF00501.35)
  • 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 COG0318
  • Curated reference: UniProt O33185 (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 — 146 functional partner(s); context anchor Rv2876
  • Primary literature: none located yet; annotation rests on the domain/homology sources above.

Ancestral MTBC0 protein sequence

>mtbc0_001791|Rv1683|
MVDLNFSMVTRPIERLVATAQNGLEVLRLGGLETGSVPSPSQIVESVPMYKLRRYFPPDNRPGQPPVGPPVLMVHPMMMSADMWDVTREDGAVGILHASGLDPWVIDFGSPDEVEGGMRRNLADHIVALSEAVDTVKDATGHDVHFVGYSQGGMFCYQAAAYRRSKDIASVVAFGSPVDTLAALPMGIPANMGAAVADFMADHVFNRLDIPSWMARMGFQMMDPLKTAKARVDFVRQLHDREALLPREQQRRFLESEGWIAWSGPAISELLKQFIAHNRMMTGGFAISGQMVTLTDITCPILAFVGEVDDIGQPASVRGIRRAAPNSEVYECLIRAGHFGLVVGSRAAQQSWPTVADWVRWISGDGTKPENIHLMADQPAEHTDSGVAFSSRVAHGIGEVSEAALALARGAADAVVAANRSVRTLAVETVRTLPRLARLGQLNDHTRISLGRIIDEQAHDAPKGEFLLFDGRVHTYEAVNRRINNVVRGLIAVGVRQGDRVGVLMETRPSALVAIAALSRLGAVAVVMRPDTDLSASVRLGRVTEILTDPTNLDAARQLPGQVLVLGGGESRDLDLPADALEQGQVIDMEKIDPDAVELPAWYRPNPGLARDLAFIAFSSADGDLVAKQITNYRWAVSAFGTASTAALGRRDTVYCLTPLHHESALLVSLGGAVVGGTRIALSRGLRPDRFVAEVRQYGVTVVSYTWAMLRDVVDDPAFVLHGNHPVRLFIGSGMPTGLWERVVEAFAPAHVVEFFATTDGQAVLANVAGAKIGSKGRPLPGAGRVELGAYDAEHDLILENDRGFVQVAGVNQVGVLLAQSRGPIDPTASVKRGVFAPADTWISTDYLFWRDDDGDYWLAGGRGSVVRTARGMVYTEPVTNALGLITGVDLAVTYGVLVRGRHVAVSAVTLLPGATITAADLTEAVASMPVGLGPDIVHVVPQLTLSGTYRPTVSALRANGIPKAGRQAWYFNSGGNEYRRLTPAVRTELTGQHRRGNA