lipoamide

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.

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Introduction

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.

What diseases are associated with lipoamide?

lipoamide 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 lipoamide

MeSH term MeSH ID Detail
Body Weight D001835 333 associated lipids
Prostatic Neoplasms D011471 126 associated lipids
Liver Cirrhosis, Biliary D008105 12 associated lipids
Nerve Degeneration D009410 53 associated lipids
Hyperglycinemia, Nonketotic D020158 2 associated lipids
Total 5

PubChem Associated disorders and diseases

What pathways are associated with lipoamide

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 lipoamide?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with lipoamide?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with lipoamide?

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

What genes are associated with lipoamide?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with lipoamide?

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

NCBI Entrez Crosslinks

All references with lipoamide

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Authors Title Published Journal PubMed Link
Nishio A et al. Primary biliary cirrhosis: lessons learned from an organ-specific disease. 2001 Clin. Exp. Med. pmid:11918275
pmid:11935326
Hengeveld AF and de Kok A Structural basis of the dysfunctioning of human 2-oxo acid dehydrogenase complexes. 2002 Curr. Med. Chem. pmid:11945122
Cronan JE Interchangeable enzyme modules. Functional replacement of the essential linker of the biotinylated subunit of acetyl-CoA carboxylase with a linker from the lipoylated subunit of pyruvate dehydrogenase. 2002 J. Biol. Chem. pmid:11956202
Huang S et al. Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein. 2002 Biophys. J. pmid:11964266
Gao H et al. The E1beta and E2 subunits of the Bacillus subtilis pyruvate dehydrogenase complex are involved in regulation of sporulation. 2002 J. Bacteriol. pmid:11976308
Omelchenko MV et al. Recurrent intragenomic recombination leading to sequence homogenization during the evolution of the lipoyl-binding domain. 2002 FEMS Microbiol. Lett. pmid:12007814
Sutton I and Neuberger J Primary biliary cirrhosis: seeking the silent partner of autoimmunity. 2002 Gut pmid:12010869
Perham RN et al. Substrate channelling in 2-oxo acid dehydrogenase multienzyme complexes. 2002 Biochem. Soc. Trans. pmid:12023822
Morton DH et al. Diagnosis and treatment of maple syrup disease: a study of 36 patients. 2002 Pediatrics pmid:12042535
pmid:12070266
pmid:12075488
Dursun A et al. Maple syrup urine disease: mutation analysis in Turkish patients. 2002 J. Inherit. Metab. Dis. pmid:12118532
Porras P et al. Glutaredoxins catalyze the reduction of glutathione by dihydrolipoamide with high efficiency. 2002 Biochem. Biophys. Res. Commun. pmid:12135599
pmid:12163191
Lynch CJ et al. Tissue-specific effects of chronic dietary leucine and norleucine supplementation on protein synthesis in rats. 2002 Am. J. Physiol. Endocrinol. Metab. pmid:12217901
Nellis MM et al. Insulin increases branched-chain alpha-ketoacid dehydrogenase kinase expression in Clone 9 rat cells. 2002 Am. J. Physiol. Endocrinol. Metab. pmid:12217904
Mooney BP et al. The complex fate of alpha-ketoacids. 2002 Annu Rev Plant Biol pmid:12221980
pmid:12227466
Owen R et al. Gene therapy for pyruvate dehydrogenase E1alpha deficiency using recombinant adeno-associated virus 2 (rAAV2) vectors. 2002 Mol. Ther. pmid:12231176