MeSH term | MeSH ID | Detail |
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Parkinsonian Disorders | D020734 | 20 associated lipids |
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.
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.
Dihydrolipoamide is suspected in and other diseases in descending order of the highest number of associated sentences.
Disease | Cross reference | Weighted score | Related literature |
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We collected disease MeSH terms mapped to the references associated with Dihydrolipoamide
MeSH term | MeSH ID | Detail |
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Parkinsonian Disorders | D020734 | 20 associated lipids |
There are no associated biomedical information in the current reference collection.
Associated locations are in red color. Not associated locations are in black.
Location | Cross reference | Weighted score | Related literatures |
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Function | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Gene | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Authors | Title | Published | Journal | PubMed Link |
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Lu X et al. | The intra- and extracellular proteome of Aspergillus niger growing on defined medium with xylose or maltose as carbon substrate. | 2010 | Microb. Cell Fact. | pmid:20406453 |
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 |
Oliver HF et al. | Deep RNA sequencing of L. monocytogenes reveals overlapping and extensive stationary phase and sigma B-dependent transcriptomes, including multiple highly transcribed noncoding RNAs. | 2009 | BMC Genomics | pmid:20042087 |
Schriek S et al. | Detection of an L-amino acid dehydrogenase activity in Synechocystis sp. PCC 6803. | 2009 | J. Exp. Bot. | pmid:19213808 |
Lee HM et al. | Impaired mitochondrial respiration and protein nitration in the rat hippocampus after acute inhalation of combustion smoke. | 2009 | Toxicol. Appl. Pharmacol. | pmid:19133281 |
Murphy MP | How mitochondria produce reactive oxygen species. | 2009 | Biochem. J. | pmid:19061483 |
Laia ML et al. | New genes of Xanthomonas citri subsp. citri involved in pathogenesis and adaptation revealed by a transposon-based mutant library. | 2009 | BMC Microbiol. | pmid:19149882 |
Brautigam CA et al. | Subunit and catalytic component stoichiometries of an in vitro reconstituted human pyruvate dehydrogenase complex. | 2009 | J. Biol. Chem. | pmid:19240034 |
Xi Y et al. | Analysis on relationship between extreme pathways and correlated reaction sets. | 2009 | BMC Bioinformatics | pmid:19208161 |
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 |