Lipoamide is a lipid of Fatty Acyls (FA) class. Lipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Phosphorylation, Protonation, Mutagenesis, Site-Directed, Oxidants and Acetylation. Lipoamide often locates in Mitochondria, Mitochondrial matrix, nucleocapsid location and Chloroplasts. The associated genes with lipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, alanylproline and Genes, Mitochondrial.
To understand associated biological information of lipoamide, 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.
lipoamide is suspected in and other diseases in descending order of the highest number of associated sentences.
| Disease | Cross reference | Weighted score | Related literature |
|---|
We collected disease MeSH terms mapped to the references associated with lipoamide
| MeSH term | MeSH ID | Detail |
|---|---|---|
| Hyperglycinemia, Nonketotic | D020158 | 2 associated lipids |
| Liver Cirrhosis, Biliary | D008105 | 12 associated lipids |
| Nerve Degeneration | D009410 | 53 associated lipids |
| Prostatic Neoplasms | D011471 | 126 associated lipids |
| Body Weight | D001835 | 333 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 |
|---|
| Function | Cross reference | Weighted score | Related literatures |
|---|
There are no associated biomedical information in the current reference collection.
| Gene | Cross reference | Weighted score | Related literatures |
|---|
There are no associated biomedical information in the current reference collection.
| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Shaler CR et al. | Understanding delayed T-cell priming, lung recruitment, and airway luminal T-cell responses in host defense against pulmonary tuberculosis. | 2012 | Clin. Dev. Immunol. | pmid:22545059 |
| Pancaldi V et al. | Predicting the fission yeast protein interaction network. | 2012 | G3 (Bethesda) | pmid:22540037 |
| Tam TK et al. | In situ regeneration of NADH via lipoamide dehydrogenase-catalyzed electron transfer reaction evidenced by spectroelectrochemistry. | 2012 | Bioelectrochemistry | pmid:22497727 |
| Ngamskulrungroj P et al. | Differences in nitrogen metabolism between Cryptococcus neoformans and C. gattii, the two etiologic agents of cryptococcosis. | 2012 | PLoS ONE | pmid:22479580 |
| Brown G | Pyruvate dehydrogenase deficiency and the brain. | 2012 | Dev Med Child Neurol | pmid:22409661 |
| Eskra L et al. | Differential expression of iron acquisition genes by Brucella melitensis and Brucella canis during macrophage infection. | 2012 | PLoS ONE | pmid:22403618 |
| Kennedy BW et al. | Probing lactate dehydrogenase activity in tumors by measuring hydrogen/deuterium exchange in hyperpolarized l-[1-(13)C,U-(2)H]lactate. | 2012 | J. Am. Chem. Soc. | pmid:22316419 |
| Li Y et al. | Five new amicoumacins isolated from a marine-derived bacterium Bacillus subtilis. | 2012 | Mar Drugs | pmid:22412803 |
| Lam AK et al. | Quantitative imaging of electron transfer flavoprotein autofluorescence reveals the dynamics of lipid partitioning in living pancreatic islets. | 2012 | Integr Biol (Camb) | pmid:22733276 |
| Wang YP et al. | Two novel mutations in the BCKDHB gene (R170H, Q346R) cause the classic form of maple syrup urine disease (MSUD). | 2012 | Gene | pmid:22326532 |