Alanine from pyruvate. Medical search. Frequent questions

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Anatomy12

Liver Mitochondria Mitochondria, Liver Muscles Myocardium Mitochondria, Muscle Cell Line Mitochondria, Heart Cytosol Cell-Free System Cells, Cultured Kidney

Organisms11

Escherichia coli Rats, Inbred Strains Zymomonas Geobacillus stearothermophilus Saccharomyces cerevisiae Rabbits Rats, Wistar Swine Rats, Sprague-Dawley Cattle Rhizobium etli

Diseases8

Pyruvate Dehydrogenase Complex Deficiency Disease Starvation Pyruvate Metabolism, Inborn Errors Pyruvate Carboxylase Deficiency Disease Drug-Induced Liver Injury Acidosis, Lactic Anemia, Hemolytic, Congenital Anemia, Hemolytic, Congenital Nonspherocytic

Chemicals and Drugs157

Alanine Pyruvate Kinase Pyruvate Dehydrogenase Complex Pyruvic Acid Pyruvates Pyruvate Decarboxylase Pyruvate Oxidase Alanine Transaminase Pyruvate Dehydrogenase (Lipoamide)Alanine Racemase Alanine Dehydrogenase Pyruvate Dehydrogenase (Lipoamide)-Phosphatase Lactates Lactic Acid Phosphoenolpyruvate Glucose Thiamine Pyrophosphate Dichloroacetic Acid Malates Dihydrolipoyllysine-Residue Acetyltransferase Oxaloacetic Acid Amino Acids Oxaloacetates Carbon Isotopes Acetates Ketone Oxidoreductases Aspartate Aminotransferases Transaminases L-Lactate Dehydrogenase Ketoglutaric Acids NAD Adenosine Triphosphate Glutamine Acetoacetates Citrates Aspartic Acid Hydroxybutyrates Ketoglutarate Dehydrogenase Complex Keto Acids Dihydrolipoamide Dehydrogenase Coenzyme A Acetyltransferases Malate Dehydrogenase Coumaric Acids Carbon Dioxide Carboxy-Lyases Glyoxylates Serine Thioctic Acid Glutamates Ketone Bodies Formates Adenosine Diphosphate Dihydroxyacetone Succinates Aminooxyacetic Acid Fructosediphosphates Culture Media Propionates Recombinant Proteins Isoenzymes Oxamic Acid Monocarboxylic Acid Transporters Caprylates Glucagon Phosphofructokinase-1 Insulin Glycerol Glutamic Acid Glycine Carbon Radioisotopes Ammonia Carboxylic Acids Phenylpyruvic Acids Biotin Adenine Nucleotides Cysteine Fatty Acids Magnesium Oxo-Acid-Lyases Bacterial Proteins Carbon Phosphoenolpyruvate Carboxykinase (GTP)Leucine Threonine Phosphates Carnitine Protein Kinases Fructose Hexokinase Fluoroacetates NADP Succinic Acid Fumarates Acetoin Citric Acid Fructose-Bisphosphate Aldolase Glycogen Citrate (si)-Synthase Lysine Proline Bicarbonates Protein-Serine-Threonine Kinases Histidine Hydrogen Hexosediphosphates Rutamycin Butanones Valine Trioses Phosphotransferases (Paired Acceptors)Peptides Isocitrates Liver Glycogen Isoleucine 3-Hydroxybutyric Acid Phosphotransferases Nitrogen Hexosephosphates Aldehyde-Lyases gamma-Glutamyltransferase Ethanol Butyrates Lactate Dehydrogenases Pyridoxal Phosphate Fructosephosphates Picolinic Acids Phenylalanine Transketolase Isocitrate Dehydrogenase Cycloserine Multienzyme Complexes Phosphoenolpyruvate Carboxylase Blood Glucose DNA Primers Glycerophosphates Acrylates Malonates Oxygen Glutamate Dehydrogenase Oligomycins Rotenone Cinnamates Macromolecular Substances RNA, Transfer, Ala Amino Acid Oxidoreductases Fructose-Bisphosphatase Tricarboxylic Acids Dicarboxylic Acids Glyceraldehyde-3-Phosphate Dehydrogenases Arginine DNA, Bacterial Oxidoreductases Ligases Glyceraldehyde 3-Phosphate Acetolactate Synthase RNA, Messenger

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Mutagenesis, Site-Directed Amino Acid Substitution Magnetic Resonance Spectroscopy Models, Molecular Culture Media Cloning, Molecular Perfusion Sequence Alignment Electrophoresis, Polyacrylamide Gel Models, Biological Spectrophotometry Crystallography, X-Ray Circular Dichroism Enzyme Stability Liver Function Tests Models, Chemical Chromatography, Gel

Psychiatry and Psychology1

Phenomena and Processes47

Citric Acid Cycle Kinetics Gluconeogenesis Glycolysis Amino Acid Sequence Decarboxylation Binding Sites Oxidation-Reduction Mutation Amino Acid Substitution Hydrogen-Ion Concentration Oxygen Consumption Base Sequence Anaerobiosis Substrate Specificity Protein Binding Fermentation Protein Conformation Energy Metabolism Sequence Homology, Amino Acid Catalysis Structure-Activity Relationship Carbohydrate Metabolism Phosphorylation Protein Structure, Tertiary Enzyme Activation Aerobiosis Time Factors Biological Transport Oxidative Phosphorylation Point Mutation Molecular Weight Temperature Protein Structure, Secondary Mutagenesis Catalytic Domain Gene Expression Regulation, Enzymologic Plasmids Conserved Sequence Enzyme Stability Allosteric Regulation Chemical Phenomena Genes, Bacterial Stereoisomerism Amino Acid Motifs Metabolic Networks and Pathways Fasting

Disciplines and Occupations1

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Health Care1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Information Science Health Care

Alanine Pyruvate Kinase Pyruvate Dehydrogenase Complex Pyruvic Acid Pyruvates Pyruvate Decarboxylase Pyruvate Oxidase Alanine Transaminase Pyruvate Dehydrogenase (Lipoamide)Alanine Racemase Alanine Dehydrogenase Pyruvate Dehydrogenase (Lipoamide)-Phosphatase Lactates Lactic Acid Phosphoenolpyruvate Glucose Citric Acid Cycle Kinetics Gluconeogenesis Thiamine Pyrophosphate Molecular Sequence Data Glycolysis Pyruvate Dehydrogenase Complex Deficiency Disease Amino Acid Sequence Dichloroacetic Acid Malates Dihydrolipoyllysine-Residue Acetyltransferase Liver Oxaloacetic Acid Amino Acids Oxaloacetates Carbon Isotopes Acetates Mutagenesis, Site-Directed Ketone Oxidoreductases Aspartate Aminotransferases Transaminases L-Lactate Dehydrogenase Ketoglutaric Acids Decarboxylation Starvation NAD Escherichia coli Binding Sites Oxidation-Reduction Adenosine Triphosphate Glutamine Acetoacetates Mutation Citrates Amino Acid Substitution Magnetic Resonance Spectroscopy Aspartic Acid Hydroxybutyrates Ketoglutarate Dehydrogenase Complex Keto Acids Dihydrolipoamide Dehydrogenase Coenzyme A Acetyltransferases Pyruvate Metabolism, Inborn Errors Hydrogen-Ion Concentration Malate Dehydrogenase Coumaric Acids Carbon Dioxide Carboxy-Lyases Oxygen Consumption Glyoxylates Serine Mitochondria Base Sequence Thioctic Acid Glutamates Models, Molecular Mitochondria, Liver Ketone Bodies Anaerobiosis Formates Adenosine Diphosphate Rats, Inbred Strains Dihydroxyacetone Succinates Substrate Specificity Aminooxyacetic Acid Fructosediphosphates Protein Binding Fermentation Culture Media Protein Conformation Energy Metabolism Propionates Recombinant Proteins Isoenzymes Oxamic Acid Monocarboxylic Acid Transporters Sequence Homology, Amino Acid Catalysis Caprylates Glucagon Phosphofructokinase-1 Insulin

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