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
Ajith VK and Prasad R A novel protein that binds to dnrN-dnrO intergenic region of Streptomyces peucetius purified by DNA affinity capture has dihydrolipoamide dehydrogenase activity. 2009 Protein Expr. Purif. pmid:19481152
Oliver HF et al. Deep RNA sequencing of L. monocytogenes reveals overlapping and extensive stationary phase and sigma B-dependent transcriptomes, including multiple highly transcribed noncoding RNAs. 2009 BMC Genomics pmid:20042087
Schriek S et al. Detection of an L-amino acid dehydrogenase activity in Synechocystis sp. PCC 6803. 2009 J. Exp. Bot. pmid:19213808
Wu TF et al. Proteomic investigation of the impact of oxygen on the protein profiles of hyaluronic acid-producing Streptococcus zooepidemicus. 2009 Proteomics pmid:19688725
Bull TJ et al. A rhodanine agent active against non-replicating intracellular Mycobacterium avium subspecies paratuberculosis. 2009 Gut Pathog pmid:20030828
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Yan LJ and Forster MJ Resolving mitochondrial protein complexes using nongradient blue native polyacrylamide gel electrophoresis. 2009 Anal. Biochem. pmid:19348780
Keyes BE and Burke DJ Irc15 Is a microtubule-associated protein that regulates microtubule dynamics in Saccharomyces cerevisiae. 2009 Curr. Biol. pmid:19285398
Lee HM et al. Impaired mitochondrial respiration and protein nitration in the rat hippocampus after acute inhalation of combustion smoke. 2009 Toxicol. Appl. Pharmacol. pmid:19133281
Murphy MP How mitochondria produce reactive oxygen species. 2009 Biochem. J. pmid:19061483
Ramos EI et al. 2,3-diphenyl-1,4-naphthoquinone: a potential chemotherapeutic agent against Trypanosoma cruzi. 2009 J. Parasitol. pmid:18788881
Laia ML et al. New genes of Xanthomonas citri subsp. citri involved in pathogenesis and adaptation revealed by a transposon-based mutant library. 2009 BMC Microbiol. pmid:19149882
Brautigam CA et al. Subunit and catalytic component stoichiometries of an in vitro reconstituted human pyruvate dehydrogenase complex. 2009 J. Biol. Chem. pmid:19240034
Xi Y et al. Analysis on relationship between extreme pathways and correlated reaction sets. 2009 BMC Bioinformatics pmid:19208161
Chi F et al. Identification of IbeR as a stationary-phase regulator in meningitic Escherichia coli K1 that carries a loss-of-function mutation in rpoS. 2009 J. Biomed. Biotechnol. pmid:19300523
Wang Q et al. Genome sequence of the versatile fish pathogen Edwardsiella tarda provides insights into its adaptation to broad host ranges and intracellular niches. 2009 PLoS ONE pmid:19865481
Li J et al. Pivotal role of the C-terminal DW-motif in mediating inhibition of pyruvate dehydrogenase kinase 2 by dichloroacetate. 2009 J. Biol. Chem. pmid:19833728
Tyagi TK et al. Moonlighting protein in Starkeyomyces koorchalomoides: characterization of dihydrolipoamide dehydrogenase as a protein acetyltransferase utilizing acetoxycoumarin as the acetyl group donor. 2009 Biochimie pmid:19383527
Griffin JL and Des Rosiers C Applications of metabolomics and proteomics to the mdx mouse model of Duchenne muscular dystrophy: lessons from downstream of the transcriptome. 2009 Genome Med pmid:19341503