Dihydrolipoamide

Dihydrolipoamide is a lipid of Fatty Acyls (FA) class. Dihydrolipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Citric Acid Cycle, Electron Transport, NADH oxidation, Oxidation and Oxidants. Dihydrolipoamide often locates in Mitochondria, Mitochondrial matrix and Chloroplasts. The associated genes with Dihydrolipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, Genes, Mitochondrial and alanylproline.

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Introduction

To understand associated biological information of Dihydrolipoamide, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Dihydrolipoamide?

Dihydrolipoamide is suspected in and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Dihydrolipoamide

MeSH term MeSH ID Detail
Parkinsonian Disorders D020734 20 associated lipids
Total 1

PubChem Associated disorders and diseases

What pathways are associated with Dihydrolipoamide

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Dihydrolipoamide?

Related references are published most in these journals:

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What functions are associated with Dihydrolipoamide?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Dihydrolipoamide?

There are no associated biomedical information in the current reference collection.

What genes are associated with Dihydrolipoamide?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Dihydrolipoamide?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with Dihydrolipoamide

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Authors Title Published Journal PubMed Link
Da Sylva TR et al. Somatic mutations in the mitochondria of rheumatoid arthritis synoviocytes. 2005 Arthritis Res. Ther. pmid:15987486
Tsiveriotis K et al. Antineutrophil cytoplasmic antibodies testing in a large cohort of unselected greek patients. 2011 Autoimmune Dis pmid:21687647
Porras P et al. Glutaredoxins catalyze the reduction of glutathione by dihydrolipoamide with high efficiency. 2002 Biochem. Biophys. Res. Commun. pmid:12135599
Park YH and Patel MS Characterization of interactions of dihydrolipoamide dehydrogenase with its binding protein in the human pyruvate dehydrogenase complex. 2010 Biochem. Biophys. Res. Commun. pmid:20385101
Fischer A et al. Effect of selenium and vitamin E deficiency on differential gene expression in rat liver. 2001 Biochem. Biophys. Res. Commun. pmid:11444866
McCully V et al. Resolution of branched-chain oxo acid dehydrogenase complex of Pseudomonas aeruginosa PAO. 1986 Biochem. J. pmid:3085653
Murphy MP How mitochondria produce reactive oxygen species. 2009 Biochem. J. pmid:19061483
Pedrajas JR et al. Two isoforms of Saccharomyces cerevisiae glutaredoxin 2 are expressed in vivo and localize to different subcellular compartments. 2002 Biochem. J. pmid:11958675
Molina Portela MP and Stoppani AO Redox cycling of beta-lapachone and related o-naphthoquinones in the presence of dihydrolipoamide and oxygen. 1996 Biochem. Pharmacol. pmid:8573194
Song J and Jordan F Interchain acetyl transfer in the E2 component of bacterial pyruvate dehydrogenase suggests a model with different roles for each chain in a trimer of the homooligomeric component. 2012 Biochemistry pmid:22413895
Argyrou A et al. Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level. 2003 Biochemistry pmid:12590611
Argyrou A et al. The lipoamide dehydrogenase from Mycobacterium tuberculosis permits the direct observation of flavin intermediates in catalysis. 2002 Biochemistry pmid:12463758
Bryk R et al. Triazaspirodimethoxybenzoyls as selective inhibitors of mycobacterial lipoamide dehydrogenase . 2010 Biochemistry pmid:20078138
Kareyeva AV et al. Mitochondrial hydrogen peroxide production as determined by the pyridine nucleotide pool and its redox state. 2012 Biochim. Biophys. Acta pmid:22503830
Luís PB et al. Valproic acid metabolites inhibit dihydrolipoyl dehydrogenase activity leading to impaired 2-oxoglutarate-driven oxidative phosphorylation. 2007 Biochim. Biophys. Acta pmid:17706936
Jacobia SJ et al. Characterization of a missense mutation at histidine-44 in a pyruvate dehydrogenase-deficient patient. 2002 Biochim. Biophys. Acta pmid:11781147
Tyagi TK et al. Moonlighting protein in Starkeyomyces koorchalomoides: characterization of dihydrolipoamide dehydrogenase as a protein acetyltransferase utilizing acetoxycoumarin as the acetyl group donor. 2009 Biochimie pmid:19383527
Tam TK et al. In situ regeneration of NADH via lipoamide dehydrogenase-catalyzed electron transfer reaction evidenced by spectroelectrochemistry. 2012 Bioelectrochemistry pmid:22497727
Takahashi T et al. NADPH-dependent coenzyme Q reductase is the main enzyme responsible for the reduction of non-mitochondrial CoQ in cells. 2008 Biofactors pmid:19096101
Nordman T et al. Regeneration of the antioxidant ubiquinol by lipoamide dehydrogenase, thioredoxin reductase and glutathione reductase. 2003 Biofactors pmid:14695919