trans-3-Methylglutaconyl CoA isomerization-dependent protein acylation
Author:
Funder
National Heart, Lung, and Blood Institute
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference16 articles.
1. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature;Wortmann;J. Inherit. Metab. Dis.,2013
2. 3-Methylglutaric acid in energy metabolism;Jones;Clin. Chim. Acta,2020
3. Beta methylcrotonyl-CoA-carboxylase. Crystallization and some physical properties;Apitz-Castro;Eur. J. Biochem.,1970
4. Leucine loading test is only discriminative for 3-methylglutaconic aciduria due to AUH defect;Wortmann;JIMD Rep,2014
5. Metabolic biology of 3-methylglutaconic acid-uria: a new perspective;Su;J. Inherit. Metab. Dis.,2014
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1. Factors Affecting Non-Enzymatic Protein Acylation by trans-3-Methylglutaconyl Coenzyme A;Metabolites;2024-07-31
2. 3-Methylglutarylcarnitine: A biomarker of mitochondrial dysfunction;Clinica Chimica Acta;2023-11
3. Characterization of trans-3-Methylglutaconyl CoA-Dependent Protein Acylation;Metabolites;2023-07-20
4. Diversion of Acetyl CoA to 3-Methylglutaconic Acid Caused by Discrete Inborn Errors of Metabolism;Metabolites;2022-04-21
5. Role of non‐enzymatic chemical reactions in 3‐methylglutaconic aciduria;The FEBS Journal;2021-12-13
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