Dihydrolipoamide

Dihydrolipoamide is a lipid of Fatty Acyls (FA) class. Dihydrolipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Citric Acid Cycle, Electron Transport, NADH oxidation, Oxidation and Oxidants. Dihydrolipoamide often locates in Mitochondria, Mitochondrial matrix and Chloroplasts. The associated genes with Dihydrolipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, Genes, Mitochondrial and alanylproline.

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Introduction

To understand associated biological information of Dihydrolipoamide, 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 Dihydrolipoamide?

Dihydrolipoamide 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 Dihydrolipoamide

MeSH term MeSH ID Detail
Parkinsonian Disorders D020734 20 associated lipids
Total 1

PubChem Associated disorders and diseases

What pathways are associated with Dihydrolipoamide

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 Dihydrolipoamide?

Related references are published most in these journals:

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


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Dihydrolipoamide?

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

What genes are associated with Dihydrolipoamide?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Dihydrolipoamide?

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

NCBI Entrez Crosslinks

All references with Dihydrolipoamide

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Authors Title Published Journal PubMed Link
Ojha S et al. Evolution of function in the "two dinucleotide binding domains" flavoproteins. 2007 PLoS Comput. Biol. pmid:17658942
Leichert LI and Jakob U Protein thiol modifications visualized in vivo. 2004 PLoS Biol. pmid:15502869
Moran JF et al. Molecular cloning, functional characterization, and subcellular localization of soybean nodule dihydrolipoamide reductase. 2002 Plant Physiol. pmid:11788775
Chen W et al. Disruption of ptLPD1 or ptLPD2, genes that encode isoforms of the plastidial lipoamide dehydrogenase, confers arsenate hypersensitivity in Arabidopsis. 2010 Plant Physiol. pmid:20488895
Lutziger I and Oliver DJ Characterization of two cDNAs encoding mitochondrial lipoamide dehydrogenase from Arabidopsis. 2001 Plant Physiol. pmid:11598235
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
Calingasan NY et al. Influence of mitochondrial enzyme deficiency on adult neurogenesis in mouse models of neurodegenerative diseases. 2008 Neuroscience pmid:18423880
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Liu DQ et al. [Microwave coagulation at different temperatures for hepatocellular carcinoma management: efficacy evaluation by enzyme histochemical staining]. 2006 Nan Fang Yi Ke Da Xue Xue Bao pmid:16939906
Suetsugu-Maki R et al. A complement receptor C5a antagonist regulates epithelial to mesenchymal transition and crystallin expression after lens cataract surgery in mice. 2011 Mol. Vis. pmid:21541266
Vyas PM and Payne RM TAT opens the door. 2008 Mol. Ther. pmid:18362922
Rapoport M et al. TAT-mediated delivery of LAD restores pyruvate dehydrogenase complex activity in the mitochondria of patients with LAD deficiency. 2008 Mol. Ther. pmid:18362926
de Berardinis V et al. A complete collection of single-gene deletion mutants of Acinetobacter baylyi ADP1. 2008 Mol. Syst. Biol. pmid:18319726
McMillan PJ et al. The human malaria parasite Plasmodium falciparum possesses two distinct dihydrolipoamide dehydrogenases. 2005 Mol. Microbiol. pmid:15612914
Roldán A et al. Lipoamide dehydrogenase is essential for both bloodstream and procyclic Trypanosoma brucei. 2011 Mol. Microbiol. pmid:21631607
Smith AW et al. Characterization of the dihydrolipoamide dehydrogenase from Streptococcus pneumoniae and its role in pneumococcal infection. 2002 Mol. Microbiol. pmid:11972781
Pei Y et al. Plasmodium pyruvate dehydrogenase activity is only essential for the parasite's progression from liver infection to blood infection. 2010 Mol. Microbiol. pmid:20487290
Boucher IW et al. Structural and biochemical characterization of a mitochondrial peroxiredoxin from Plasmodium falciparum. 2006 Mol. Microbiol. pmid:16879648
Tian J et al. Mycobacterium tuberculosis appears to lack alpha-ketoglutarate dehydrogenase and encodes pyruvate dehydrogenase in widely separated genes. 2005 Mol. Microbiol. pmid:16045627