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
Mathias RA et al. Sirtuin 4 is a lipoamidase regulating pyruvate dehydrogenase complex activity. 2014 Cell pmid:25525879
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
Giribaldi G et al. Intermittent-relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility. 2012 Dev Med Child Neurol pmid:22142326
Tang H and Goldberg E A-MYB (MYBL1) stimulates murine testis-specific Ldhc expression via the cAMP-responsive element (CRE) site. 2012 Biol. Reprod. pmid:21998171
Sharma R et al. Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiency. 2012 Dev Med Child Neurol pmid:21895644
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