MeSH term | MeSH ID | Detail |
---|---|---|
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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Vilei EM et al. | Beta-D-glucoside utilization by Mycoplasma mycoides subsp. mycoides SC: possible involvement in the control of cytotoxicity towards bovine lung cells. | 2007 | BMC Microbiol. | pmid:17439646 |
Islam MM et al. | A novel branched-chain amino acid metabolon. Protein-protein interactions in a supramolecular complex. | 2007 | J. Biol. Chem. | pmid:17314104 |
Mochel F et al. | Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression. | 2007 | PLoS ONE | pmid:17653274 |
Chiu KP et al. | Pathway aberrations of murine melanoma cells observed in Paired-End diTag transcriptomes. | 2007 | BMC Cancer | pmid:17594473 |
Deghmane AE et al. | Lipoamide dehydrogenase mediates retention of coronin-1 on BCG vacuoles, leading to arrest in phagosome maturation. | 2007 | J. Cell. Sci. | pmid:17652161 |
Hussain SN et al. | Modifications of proteins by 4-hydroxy-2-nonenal in the ventilatory muscles of rats. | 2006 | Am. J. Physiol. Lung Cell Mol. Physiol. | pmid:16603597 |
Smolle M et al. | A new level of architectural complexity in the human pyruvate dehydrogenase complex. | 2006 | J. Biol. Chem. | pmid:16679318 |
Vasiliou V et al. | Update of the NAD(P)H:quinone oxidoreductase (NQO) gene family. | 2006 | Hum. Genomics | pmid:16595077 |
Brautigam CA et al. | Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex. | 2006 | Structure | pmid:16442803 |
Li M et al. | Effect of lpdA gene knockout on the metabolism in Escherichia coli based on enzyme activities, intracellular metabolite concentrations and metabolic flux analysis by 13C-labeling experiments. | 2006 | J. Biotechnol. | pmid:16310273 |