| scholarly article | Q13442814 |
| P50 | author | Manisha Nautiyal | Q65600769 |
| P2093 | author name string | Susan M. Hutson | |
| David T. Chuang | |||
| Mohammad Mainul Islam | |||
| James A. Mobley | |||
| R. Max Wynn | |||
| P2860 | cites work | Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations | Q24292490 |
| Cross-talk between thiamin diphosphate binding and phosphorylation loop conformation in human branched-chain alpha-keto acid decarboxylase/dehydrogenase | Q24294487 | ||
| Molecular mechanism for regulation of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase complex by phosphorylation | Q24318778 | ||
| Function of leucine in excitatory neurotransmitter metabolism in the central nervous system | Q48960400 | ||
| Detection of the swings of the lever arm of a myosin motor by fluorescence resonance energy transfer of green and blue fluorescent proteins. | Q50507536 | ||
| Physiological covalent regulation of rat liver branched-chain alpha-ketoacid dehydrogenase. | Q51635975 | ||
| Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations | Q56592981 | ||
| Comparison of the effects of leucines, non-metabolizable leucine analogues and other insulin secretagogues on the activity of glutamate dehydrogenase | Q67855971 | ||
| Regulation of substrate availability for the branched-chain alpha-keto acid dehydrogenase enzyme complex | Q69463257 | ||
| Branched chain alpha-keto acid oxidative decarboxylation in skeletal muscle mitochondria. Effect of isolation procedure and mitochondrial delta pH | Q70031437 | ||
| The binding of oxidised coenzyme to bovine-liver glutamate dehydrogenase studied by circular-difference spectroscopy | Q71474393 | ||
| Interaction of branched chain amino acids and keto acids upon pancreatic islet metabolism and insulin secretion | Q72140508 | ||
| Macromolecular interactions: tracing the roots | Q73493196 | ||
| Branched-chain amino-acid aminotransferase of Escherichia coli | Q74318111 | ||
| Production of recombinant mammalian holo-E2 and E3 and reconstitution of functional branched-chain alpha-keto acid dehydrogenase complex with recombinant E1 | Q74318135 | ||
| Mammalian branched-chain aminotransferases | Q74318160 | ||
| A novel branched-chain amino acid metabolon. Protein-protein interactions in a supramolecular complex | Q79807582 | ||
| Assembly and regulation of a glycolytic enzyme complex on the human erythrocyte membrane | Q24556643 | ||
| Application of a Theory of Enzyme Specificity to Protein Synthesis | Q24620284 | ||
| Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation | Q27630686 | ||
| The structure of human mitochondrial branched-chain aminotransferase | Q27630770 | ||
| The structure of apo human glutamate dehydrogenase details subunit communication and allostery | Q27639129 | ||
| Crystal structures of human mitochondrial branched chain aminotransferase reaction intermediates: ketimine and pyridoxamine phosphate forms | Q27639682 | ||
| Structure-function relationships in dihydrolipoamide acyltransferases | Q28247047 | ||
| Overexpression and characterization of the human mitochondrial and cytosolic branched-chain aminotransferases | Q28262954 | ||
| Human mitochondrial branched chain aminotransferase isozyme: structural role of the CXXC center in catalysis | Q28269148 | ||
| Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene | Q28269681 | ||
| Regulation of mammalian pyruvate and branched-chain alpha-keto acid dehydrogenase complexes by phosphorylation-dephosphorylation | Q28287050 | ||
| Feasibility of pathways for transfer of acyl groups from mitochondria to the cytosol to form short chain acyl-CoAs in the pancreatic beta cell | Q28565418 | ||
| Escherichia coli aromatic amino acid aminotransferase: characterization and comparison with aspartate aminotransferase | Q30421365 | ||
| Identification of protein fragments as pattern features in MALDI-MS analyses of serum | Q33224829 | ||
| Folding funnels and binding mechanisms | Q33743626 | ||
| A trail of research from lipoic acid to alpha-keto acid dehydrogenase complexes | Q33953799 | ||
| A versatile conformational switch regulates reactivity in human branched-chain alpha-ketoacid dehydrogenase | Q33993506 | ||
| Identification of a peroxide-sensitive redox switch at the CXXC motif in the human mitochondrial branched chain aminotransferase. | Q34138951 | ||
| Reversible compartmentalization of de novo purine biosynthetic complexes in living cells | Q34767701 | ||
| Chapter 26 Preparation and Characterization of Mitochondria and Submitochondrial Particles of Rat Liver and Liver-Derived Tissues | Q35760521 | ||
| New insights into amino acid metabolism, beta-cell function and diabetes | Q35950524 | ||
| Alanine and inter-organ relationships in branched-chain amino and 2-oxo acid metabolism. Review | Q39851055 | ||
| Studies with leucine, beta-hydroxybutyrate and ATP citrate lyase-deficient beta cells support the acetoacetate pathway of insulin secretion | Q39988003 | ||
| Circular dichroism of complexes of NADH with self-associating bovine liver glutamate dehydrogenase | Q40284840 | ||
| Unregulated insulin secretion by pancreatic beta cells in hyperinsulinism/hyperammonemia syndrome: role of glutamate dehydrogenase, ATP-sensitive potassium channel, and nonselective cation channel | Q40313259 | ||
| Distinguishing Features of Leucine and α-Ketoisocaproate Sensing in Pancreatic β-Cells | Q40655102 | ||
| Expression of E1 component of human branched-chain alpha-keto acid dehydrogenase complex in Escherichia coli by cotransformation with chaperonins GroEL and GroES. | Q40855004 | ||
| Role of the pleiotropic effects of plasminogen deficiency in infection experiments with plasminogen-deficient mice | Q41479556 | ||
| L-leucine and a nonmetabolized analogue activate pancreatic islet glutamate dehydrogenase | Q41614642 | ||
| Purification of branched chain aminotransferase from rat heart mitochondria | Q42631433 | ||
| Ox glutamate dehydrogenase. Comparison of the kinetic properties of native and proteolysed preparations | Q42866212 | ||
| Potential role of leucine metabolism in the leucine-signaling pathway involving mTOR. | Q44482073 | ||
| Branched-chain amino acid catabolism: unique segregation of pathway enzymes in organ systems and peripheral nerves | Q44579245 | ||
| Roles for cysteine residues in the regulatory CXXC motif of human mitochondrial branched chain aminotransferase enzyme | Q44925085 | ||
| Reactive amino acid residues involved in glutamate-binding of human glutamate dehydrogenase isozymes | Q44934128 | ||
| Regulation of leucine and alpha-ketoisocaproate metabolism in skeletal muscle | Q44987034 | ||
| Uptake of individual amino acids by the human brain | Q45070352 | ||
| Evolution of glutamate dehydrogenase regulation of insulin homeostasis is an example of molecular exaptation | Q45143788 | ||
| Identification of ADP-ribosylation site in human glutamate dehydrogenase isozymes | Q46603315 | ||
| A molecular model of human branched-chain amino acid metabolism | Q46762438 | ||
| Nonfibrinolytic functions of plasminogen | Q47865721 | ||
| Tissue heterogeneity of the mammalian mitochondrial proteome | Q48439191 | ||
| Pyruvate carboxylase | Q48464317 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mitochondrion | Q39572 |
| P304 | page(s) | 265–276 | |
| P577 | publication date | 2010-01-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Branched-chain amino acid metabolon: interaction of glutamate dehydrogenase with the mitochondrial branched-chain aminotransferase (BCATm) | |
| P478 | volume | 285 |
| Q33756201 | 13N as a tracer for studying glutamate metabolism |
| Q33671504 | Altered Metabolic Profiles Associate with Toxicity in SOD1G93A Astrocyte-Neuron Co-Cultures. |
| Q89669785 | Alzheimer's disease: targeting the glutamatergic system |
| Q38130674 | Astrocytic Control of Biosynthesis and Turnover of the Neurotransmitters Glutamate and GABA. |
| Q46454853 | BCAA Metabolism and NH3 Homeostasis |
| Q93371887 | Branched Chain Amino Acids |
| Q39247363 | Branched-Chain Amino Acids and Brain Metabolism |
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| Q34173724 | Compartmentalization and molecular traffic in secondary metabolism: a new understanding of established cellular processes |
| Q54252125 | Contribution of branched-chain amino acids to purine nucleotide cycle: a pilot study. |
| Q92587584 | Crystal structure of an oxidized mutant of human mitochondrial branched-chain aminotransferase |
| Q33969545 | Cysteine S-conjugate β-lyases: important roles in the metabolism of naturally occurring sulfur and selenium-containing compounds, xenobiotics and anticancer agents. |
| Q53076231 | Detecting Purinosome Metabolon Formation with Fluorescence Microscopy. |
| Q50085899 | Determination of Branched-Chain Keto Acids in Serum and Muscles Using High Performance Liquid Chromatography-Quadrupole Time-of-Flight Mass Spectrometry. |
| Q34304403 | Distribution of the branched chain aminotransferase proteins in the human brain and their role in glutamate regulation. |
| Q57901307 | Dysfunctional TCA-Cycle Metabolism in Glutamate Dehydrogenase Deficient Astrocytes |
| Q44186891 | Elevated levels of branched-chain amino acids have little effect on pancreatic islet cells, but L-arginine impairs function through activation of the endoplasmic reticulum stress response |
| Q48417490 | Enzyme Complexes Important for the Glutamate-Glutamine Cycle |
| Q47245807 | Expression of the human isoform of glutamate dehydrogenase, hGDH2, augments TCA cycle capacity and oxidative metabolism of glutamate during glucose deprivation in astrocytes |
| Q46342878 | Genome-wide analysis of branched-chain amino acid levels in Arabidopsis seeds. |
| Q37902770 | Glutamate dehydrogenase in brain mitochondria: do lipid modifications and transient metabolon formation influence enzyme activity? |
| Q39008261 | Glutamate formation via the leucine-to-glutamate pathway of rat pancreas |
| Q43145476 | Glutamate metabolism in the brain focusing on astrocytes. |
| Q35386044 | Independent evolutionary origins of functional polyamine biosynthetic enzyme fusions catalysing de novo diamine to triamine formation |
| Q45047747 | Liver BCATm transgenic mouse model reveals the important role of the liver in maintaining BCAA homeostasis |
| Q39003510 | Management of Multiple Nitrogen Sources during Wine Fermentation by Saccharomyces cerevisiae |
| Q26801523 | Milk--A Nutrient System of Mammalian Evolution Promoting mTORC1-Dependent Translation |
| Q38228592 | Mitochondrial function and mitochondrial DNA maintenance with advancing age. |
| Q35140265 | Mitochondrial malic enzyme 3 is important for insulin secretion in pancreatic β-cells |
| Q36106917 | Mitochondrial nucleoid interacting proteins support mitochondrial protein synthesis. |
| Q37932454 | Neuron-glia interactions in glutamatergic neurotransmission: roles of oxidative and glycolytic adenosine triphosphate as energy source |
| Q38339439 | New insights into the role of the branched-chain aminotransferase proteins in the human brain |
| Q37193192 | Olanzapine activates hepatic mammalian target of rapamycin: new mechanistic insight into metabolic dysregulation with atypical antipsychotic drugs |
| Q36672821 | Placental stem cell correction of murine intermediate maple syrup urine disease |
| Q38078273 | Role of branched chain amino acids in cerebral ammonia homeostasis related to hepatic encephalopathy. |
| Q39350533 | Spatial Organization of Metabolic Enzyme Complexes in Cells |
| Q27027262 | The pathogenic role of persistent milk signaling in mTORC1- and milk-microRNA-driven type 2 diabetes mellitus |
| Q37950871 | The role of glutamate dehydrogenase in mammalian ammonia metabolism |
| Q38036825 | Translocation of solutes and proteins across the glycosomal membrane of trypanosomes; possibilities and limitations for targeting with trypanocidal drugs. |
| Q90927935 | Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria |
| Q28306320 | Two novel mutations in the BCKDK (branched-chain keto-acid dehydrogenase kinase) gene are responsible for a neurobehavioral deficit in two pediatric unrelated patients |
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