Biotin metabolism, including IMDs (WP5031)
Homo sapiens
Authors
Denise Slenter , Egon Willighagen , Eric Weitz , and Finterly HuCited In
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Organism
Homo sapiensCommunities
Inherited Metabolic Disorders (IMD) Pathways Rare DiseasesAnnotations
Disease Ontology: 3-Methylcrotonyl-CoA carboxylase 2 deficiency pyruvate carboxylase deficiency disease 3-Methylcrotonyl-CoA carboxylase 1 deficiency 3-Methylcrotonyl-CoA carboxylase deficiency holocarboxylase synthetase deficiency biotinidase deficiency
Pathway Ontology: 3-methylcrotonyl CoA carboxylase 2 deficiency pathway 3-methylcrotonyl CoA carboxylase 1 deficiency pathway biotin metabolic pathway holocarboxylase synthetase deficiency pathway biotinidase deficiency pathway pyruvate carboxylase deficiency pathway
Participants
Label | Type | Compact Identifier | Comment |
---|---|---|---|
pyruvate | Metabolite | chebi:15361 | |
Apo-ACC | Metabolite | chebi:29969 | aka apo-[methylmalonyl-CoA:pyruvate carboxytransferase] |
propanoyl-CoA | Metabolite | chebi:57392 | aka propionyl-CoA |
leucine | Metabolite | chebi:25017 | |
oxaloacetate | Metabolite | chebi:16452 | |
3-methylglutaconyl-CoA | Metabolite | chebi:57346 | aka trans-3-methylglutaconyl-CoA |
3-methylcrotonyl-COA | Metabolite | chebi:57344 | aka 3-methylbut-2-enoyl-CoA |
Dietary and otherprotein-bound biotin | Metabolite | chebi:16615 | |
Biocytin | Metabolite | wikidata:Q864247 | biotin covalantly bound to lysine |
Lysine | Metabolite | chebi:25094 | |
free biotin | Metabolite | chebi:15956 | |
Acetyl-CoA | Metabolite | chebi:57288 | |
Biotin (free pool) | Metabolite | chebi:15956 | |
Malonyl-CoA | Metabolite | chebi:57384 | |
holo-ACC | Metabolite | chebi:83144 | aka holo-[methylmalonyl-CoA:pyruvate carboxytransferase] |
Apo-PCC | Metabolite | chebi:29969 | aka apo-[propionyl-CoA:carbon-dioxide ligase (ADP-forming)] |
holo-PCC | Metabolite | chebi:83144 | aka holo-[propionyl-CoA:carbon-dioxide ligase (ADP-forming)] |
Apo-MCC | Metabolite | chebi:29969 | aka apo-[3-methylcrotonoyl-CoA:carbon-dioxide ligase (ADP-forming)] |
holo-MCC | Metabolite | chebi:83144 | aka holo-[3-methylcrotonoyl-CoA:carbon-dioxide ligase (ADP-forming)] |
Apo-PC | Metabolite | chebi:29969 | aka pyruvate carboxylase |
holo-PC | Metabolite | chebi:83144 | aka pyruvate carboxylase |
Biotin | Metabolite | chebi:15956 | |
methylmanoyl-CoA | Metabolite | chebi:57327 | |
PC | Protein | uniprot:P11498 | aka pyruvate carboxylase |
MCCC1 | Protein | uniprot:Q96RQ3 | |
Biotinidase (BTD) | Protein | uniprot:P43251 | |
HLCS | Protein | uniprot:P50747 | aka Holocarboxylase Synthetase |
ACC1(cytosol) | Protein | uniprot:Q13085 | aka acetyl-CoA carboxylase |
ACC2(mitochondrial) | Protein | uniprot:O00763 | aka acetyl-CoA carboxylase |
MCCC2 | Protein | uniprot:Q9HCC0 | |
PCCA | Protein | uniprot:P05165 | |
PCCB | Protein | uniprot:P05166 |
References
- Blau N, Duran M, Gibson KM, Dionisi-Vici C. Physician’s Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases [Internet]. Springer; 2014. 867 p. Available from: https://books.google.com/books/about/Physician_s_Guide_to_the_Diagnosis_Treat.html?hl=&id=wJRBnwEACAAJ OpenLibrary Worldcat
- Biotinidase and its roles in biotin metabolism. Hymes J, Wolf B. Clin Chim Acta. 1996 Nov 15;255(1):1–11. PubMed Europe PMC Scholia
- Biotin: biochemical, physiological and clinical aspects. Said HM. Subcell Biochem. 2012;56:1–19. PubMed Europe PMC Scholia