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
Bryk R et al. Metabolic enzymes of mycobacteria linked to antioxidant defense by a thioredoxin-like protein. 2002 Science pmid:11799204
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
Sutton I and Neuberger J Primary biliary cirrhosis: seeking the silent partner of autoimmunity. 2002 Gut pmid:12010869
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
Fujiki Y et al. Activation of the promoters of Arabidopsis genes for the branched-chain alpha-keto acid dehydrogenase complex in transgenic tobacco BY-2 cells under sugar starvation. 2002 Plant Cell Physiol. pmid:11917081
Love-Gregory LD et al. Evidence of common ancestry for the maple syrup urine disease (MSUD) Y438N allele in non-Mennonite MSUD patients. 2002 Mol. Genet. Metab. pmid:11825067
Bunik VI and Sievers C Inactivation of the 2-oxo acid dehydrogenase complexes upon generation of intrinsic radical species. 2002 Eur. J. Biochem. pmid:12383259
Naik MT et al. Folding kinetics of the lipoic acid-bearing domain of human mitochondrial branched chain alpha-ketoacid dehydrogenase complex. 2002 FEBS Lett. pmid:12387880
Argyrou A et al. The lipoamide dehydrogenase from Mycobacterium tuberculosis permits the direct observation of flavin intermediates in catalysis. 2002 Biochemistry pmid:12463758
Nemeria N et al. Histidine 407, a phantom residue in the E1 subunit of the Escherichia coli pyruvate dehydrogenase complex, activates reductive acetylation of lipoamide on the E2 subunit. An explanation for conservation of active sites between the E1 subunit and transketolase. 2002 Biochemistry pmid:12501174
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
Dallo SF et al. Elongation factor Tu and E1 beta subunit of pyruvate dehydrogenase complex act as fibronectin binding proteins in Mycoplasma pneumoniae. 2002 Mol. Microbiol. pmid:12421310
Owen R et al. Gene therapy for pyruvate dehydrogenase E1alpha deficiency using recombinant adeno-associated virus 2 (rAAV2) vectors. 2002 Mol. Ther. pmid:12231176
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
Huang S et al. Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein. 2002 Biophys. J. pmid:11964266
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
Nicholls LI et al. Glucose-stimulated insulin secretion does not require activation of pyruvate dehydrogenase: impact of adenovirus-mediated overexpression of PDH kinase and PDH phosphate phosphatase in pancreatic islets. 2002 Biochem. Biophys. Res. Commun. pmid:11866475
Richards JG et al. Glycogen phosphorylase and pyruvate dehydrogenase transformation in white muscle of trout during high-intensity exercise. 2002 Am. J. Physiol. Regul. Integr. Comp. Physiol. pmid:11832404
Jacobia SJ et al. Characterization of a missense mutation at histidine-44 in a pyruvate dehydrogenase-deficient patient. 2002 Biochim. Biophys. Acta pmid:11781147
Gazaryan IG et al. Zinc is a potent inhibitor of thiol oxidoreductase activity and stimulates reactive oxygen species production by lipoamide dehydrogenase. 2002 J. Biol. Chem. pmid:11744691
Chang CF et al. Solution structure and dynamics of the lipoic acid-bearing domain of human mitochondrial branched-chain alpha-keto acid dehydrogenase complex. 2002 J. Biol. Chem. pmid:11839747
Bogenhagen DF et al. Protein components of mitochondrial DNA nucleoids in higher eukaryotes. 2003 Mol. Cell Proteomics pmid:14514796
Bunik VI 2-Oxo acid dehydrogenase complexes of multicellular organisms. 2003 Eur. J. Biochem. pmid:12631262
Song JL et al. Encapsulation of an 86-kDa assembly intermediate inside the cavities of GroEL and its single-ring variant SR1 by GroES. 2003 J. Biol. Chem. pmid:12431983
Raj DS et al. Markers of inflammation, proteolysis, and apoptosis in ESRD. 2003 Am. J. Kidney Dis. pmid:14655193
Fouque F et al. Differential effect of DCA treatment on the pyruvate dehydrogenase complex in patients with severe PDHC deficiency. 2003 Pediatr. Res. pmid:12621116
Vanacore N Premorbid weight, body mass, and varsity athletics in ALS. 2003 Neurology pmid:14557595
Henneke M et al. Identification of twelve novel mutations in patients with classic and variant forms of maple syrup urine disease. 2003 Hum. Mutat. pmid:14517957
Fries M et al. Reaction mechanism of the heterotetrameric (alpha2beta2) E1 component of 2-oxo acid dehydrogenase multienzyme complexes. 2003 Biochemistry pmid:12795594
Jan W et al. MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation. 2003 Neuroradiology pmid:12736767
Bunik VI 2-Oxo acid dehydrogenase complexes in redox regulation. 2003 Eur. J. Biochem. pmid:12631263
Persson HL et al. Prevention of oxidant-induced cell death by lysosomotropic iron chelators. 2003 Free Radic. Biol. Med. pmid:12726917
Zhao X et al. Assembly of the covalent linkage between lipoic acid and its cognate enzymes. 2003 Chem. Biol. pmid:14700636
Argyrou A et al. Catalysis of diaphorase reactions by Mycobacterium tuberculosis lipoamide dehydrogenase occurs at the EH4 level. 2003 Biochemistry pmid:12590611
Wynn RM et al. Roles of His291-alpha and His146-beta' in the reductive acylation reaction catalyzed by human branched-chain alpha-ketoacid dehydrogenase: refined phosphorylation loop structure in the active site. 2003 J. Biol. Chem. pmid:12902323
Nordman T et al. Regeneration of the antioxidant ubiquinol by lipoamide dehydrogenase, thioredoxin reductase and glutathione reductase. 2003 Biofactors pmid:14695919
Masignani V et al. NarE: a novel ADP-ribosyltransferase from Neisseria meningitidis. 2003 Mol. Microbiol. pmid:14617161
Fujinoki M et al. Identification of 36-kDa flagellar phosphoproteins associated with hamster sperm motility. 2003 J. Biochem. pmid:12761172
Bykova NV et al. Phosphorylation of formate dehydrogenase in potato tuber mitochondria. 2003 J. Biol. Chem. pmid:12714601
Yui R et al. Antisense inhibition of mitochondrial pyruvate dehydrogenase E1alpha subunit in anther tapetum causes male sterility. 2003 Plant J. pmid:12662309
Ciszak EM et al. Structural basis for flip-flop action of thiamin pyrophosphate-dependent enzymes revealed by human pyruvate dehydrogenase. 2003 J. Biol. Chem. pmid:12651851
Miné M et al. Splicing error in E1alpha pyruvate dehydrogenase mRNA caused by novel intronic mutation responsible for lactic acidosis and mental retardation. 2003 J. Biol. Chem. pmid:12551913
Shilo S et al. Selenite sensitizes mitochondrial permeability transition pore opening in vitro and in vivo: a possible mechanism for chemo-protection. 2003 Biochem. J. pmid:12423204
Nakai T et al. Ligand-induced conformational changes and a reaction intermediate in branched-chain 2-oxo acid dehydrogenase (E1) from Thermus thermophilus HB8, as revealed by X-ray crystallography. 2004 J. Mol. Biol. pmid:15033367
Sweatt AJ et al. Branched-chain amino acid catabolism: unique segregation of pathway enzymes in organ systems and peripheral nerves. 2004 Am. J. Physiol. Endocrinol. Metab. pmid:12965870
Meneses-Lorente G et al. A proteomic investigation of drug-induced steatosis in rat liver. 2004 Chem. Res. Toxicol. pmid:15144217
Honda T et al. Effects of liver failure on branched-chain alpha-keto acid dehydrogenase complex in rat liver and muscle: comparison between acute and chronic liver failure. 2004 J. Hepatol. pmid:15123358
Kasinski A et al. Leucine toxicity in a neuronal cell model with inhibited branched chain amino acid catabolism. 2004 Brain Res. Mol. Brain Res. pmid:15010210
Self JT et al. Glutamine synthesis in the developing porcine placenta. 2004 Biol. Reprod. pmid:14736817
Bafunno V et al. Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria: involvement of the Flx1p carrier in FAD export. 2004 J. Biol. Chem. pmid:14555654