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
Zhao L et al. Lipoamide Acts as an Indirect Antioxidant by Simultaneously Stimulating Mitochondrial Biogenesis and Phase II Antioxidant Enzyme Systems in ARPE-19 Cells. 2015 PLoS ONE pmid:26030919
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Li Y et al. Scavenging of blood glutamate for enhancing brain-to-blood glutamate efflux. 2014 Mol Med Rep pmid:24220720
Bryk R et al. Lipoamide channel-binding sulfonamides selectively inhibit mycobacterial lipoamide dehydrogenase. 2013 Biochemistry pmid:24251446
McLain AL et al. Glutathionylation of α-ketoglutarate dehydrogenase: the chemical nature and relative susceptibility of the cofactor lipoic acid to modification. 2013 Free Radic. Biol. Med. pmid:23567190
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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
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Koga Y et al. Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene. 2012 Brain Dev. pmid:21454027
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Novarino G et al. Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy. 2012 Science pmid:22956686
Zhou M et al. Tissue-specific and nutrient regulation of the branched-chain α-keto acid dehydrogenase phosphatase, protein phosphatase 2Cm (PP2Cm). 2012 J. Biol. Chem. pmid:22589535
Li Y et al. Five new amicoumacins isolated from a marine-derived bacterium Bacillus subtilis. 2012 Mar Drugs pmid:22412803
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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
Chen P et al. Dietary lipoic acid influences antioxidant capability and oxidative status of broilers. 2011 Int J Mol Sci pmid:22272085
Mayr JA et al. Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation. 2011 Am. J. Hum. Genet. pmid:22152680
Salinthone S et al. Lipoic acid stimulates cAMP production via G protein-coupled receptor-dependent and -independent mechanisms. 2011 J. Nutr. Biochem. pmid:21036588
Madawala SR et al. Novel Conjugates of 1,3-Diacylglycerol and Lipoic Acid: Synthesis, DPPH Assay, and RP-LC-MS-APCI Analysis. 2011 J Lipids pmid:21966595
Hong JK et al. Growth factor withdrawal in combination with sodium butyrate addition extends culture longevity and enhances antibody production in CHO cells. 2011 J. Biotechnol. pmid:21723342
Ferguson LR and Karunasinghe N Nutrigenetics, nutrigenomics, and selenium. 2011 Front Genet pmid:22303312
Barjaktarovic Z et al. Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays. 2011 PLoS ONE pmid:22174747
Tondo ML et al. Structural-functional characterization and physiological significance of ferredoxin-NADP reductase from Xanthomonas axonopodis pv. citri. 2011 PLoS ONE pmid:22096528
Vazquez A et al. Serine biosynthesis with one carbon catabolism and the glycine cleavage system represents a novel pathway for ATP generation. 2011 PLoS ONE pmid:22073143
Simončič M et al. Obesity resistant mechanisms in the Lean polygenic mouse model as indicated by liver transcriptome and expression of selected genes in skeletal muscle. 2011 BMC Genomics pmid:21291556
Christophersen OA and Haug A Animal products, diseases and drugs: a plea for better integration between agricultural sciences, human nutrition and human pharmacology. 2011 Lipids Health Dis pmid:21247506
Venugopal A et al. Virulence of Mycobacterium tuberculosis depends on lipoamide dehydrogenase, a member of three multienzyme complexes. 2011 Cell Host Microbe pmid:21238944
Boyle KE et al. A high-fat diet elicits differential responses in genes coordinating oxidative metabolism in skeletal muscle of lean and obese individuals. 2011 J. Clin. Endocrinol. Metab. pmid:21190973
Shen W et al. Lipoamide or lipoic acid stimulates mitochondrial biogenesis in 3T3-L1 adipocytes via the endothelial NO synthase-cGMP-protein kinase G signalling pathway. 2011 Br. J. Pharmacol. pmid:21108628
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Diebold AR et al. Activation of α-keto acid-dependent dioxygenases: application of an {FeNO}7/{FeO2}8 methodology for characterizing the initial steps of O2 activation. 2011 J. Am. Chem. Soc. pmid:21981763
Brunetti-Pierri N et al. Phenylbutyrate therapy for maple syrup urine disease. 2011 Hum. Mol. Genet. pmid:21098507
Golbidi S et al. Diabetes and alpha lipoic Acid. 2011 Front Pharmacol pmid:22125537
Park HD et al. Three Korean patients with maple syrup urine disease: four novel mutations in the BCKDHA gene. 2011 Ann. Clin. Lab. Sci. pmid:21844576
Casteel J et al. Mapping the lipoylation site of Arabidopsis thaliana plastidial dihydrolipoamide S-acetyltransferase using mass spectrometry and site-directed mutagenesis. 2011 Plant Physiol. Biochem. pmid:21798751