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1.7 A structure of FR-1, a fibroblast growth factor-induced member of the aldo-keto reductase family, complexed with coenzyme and inhibitor

Biochemistry (Easton), 1995-11, Vol.34 (44), p.14323-14330

1995

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1-Aminocyclopropanephosphonate: time-dependent inactivation of 1-aminocyclopropanecarboxylate deaminase and Bacillus stearothermophilus alanine racemase by slow dissociation behavior

Biochemistry (Easton), 1987-06, Vol.26 (12), p.3417-3425

1987

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1-Ethynylpyrene, a suicide inhibitor of cytochrome P-450 dependent benzo[a]pyrene hydroxylase activity in liver microsomes

Biochemistry (Easton), 1984-08, Vol.23 (17), p.3827-3836

1984

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13C NMR study of the stereospecificity of the thiohemiacetals formed on inhibition of papain by specific enantiomeric aldehydes

Biochemistry (Easton), 1986-04, Vol.25 (8), p.2293-2298

1986

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15N NMR Relaxation Studies of Free and Inhibitor-Bound 4-Oxalocrotonate Tautomerase: Backbone Dynamics and Entropy Changes of an Enzyme upon Inhibitor Binding

Biochemistry (Easton), 1996-12, Vol.35 (50), p.16036-16047

1996

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15N NMR spectroscopy of hydrogen-bonding interactions in the active site of serine proteases: evidence for a moving histidine mechanism

Biochemistry (Easton), 1986-11, Vol.25 (23), p.7751-7759

BACHOVCHIN, W. W

1986

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18O isotopic 13C NMR shift as proof that bifunctional peptidylglycine α-amidating enzyme is a monooxygenase

Biochemistry (Easton), 1992-08, Vol.31 (32), p.7282-7288

1992

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19F NMR investigations of the catalytic mechanism of phosphoglucomutase using fluorinated substrates and inhibitors

Biochemistry (Easton), 1992-01, Vol.31 (2), p.505-512

1992

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(±)-(1S,2R,5S)-5-Amino-2-fluorocyclohex-3-enecarboxylic Acid. A Potent GABA Aminotransferase Inactivator that Irreversibly Inhibits via an Elimination−Aromatization Pathway

Biochemistry (Easton), 2006-12, Vol.45 (48), p.14513-14522

2006

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2,3-Diphosphoglycerate phosphatase activity of phosphoglycerate mutase: stimulation by vanadate and phosphate

Biochemistry (Easton), 1987-03, Vol.26 (5), p.1264-1269

1987

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2-[(4-Bromo-2,3-dioxobutyl)thio]adenosine 5'-monophosphate, a new nucleotide analog that acts as an affinity label of pyruvate kinase

Biochemistry (Easton), 1985-12, Vol.24 (26), p.7586-7593

1985

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2'-C-Methyladenosine and 2'-C-methyluridine 5'-diphosphates are mechanism-based inhibitors of ribonucleoside diphosphate reductase from Corynebacterium nephridii

Biochemistry (Easton), 1993-10, Vol.32 (42), p.11397-11404

1993

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2'-Deoxy-2'-halonucleotides as alternate substrates and mechanism-based inactivators of Lactobacillus leichmannii ribonucleotide reductase

Biochemistry (Easton), 1987-04, Vol.26 (7), p.1895-1902

1987

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2-Octynoyl coenzyme A is a mechanism-based inhibitor of pig kidney medium-chain acyl coenzyme A dehydrogenase: isolation of the target peptide

Biochemistry (Easton), 1988-10, Vol.27 (21), p.8022-8028

1988

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2-Oxo-3-alkynoic Acids, Universal Mechanism-Based Inactivators of Thiamin Diphosphate-Dependent Decarboxylases: Synthesis and Evidence for Potent Inactivation of the Pyruvate Dehydrogenase Multienzyme Complex

Biochemistry (Easton), 1997-07, Vol.36 (26), p.8071-8081

1997

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A 23-kDa protein as a substrate for protein kinase C in bovine neutrophils. Purification and partial characterization

Biochemistry (Easton), 1989-12, Vol.28 (25), p.9659-9667

1989

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A 3,4-dichloroisocoumarin-resistant component of the multicatalytic proteinase complex

Biochemistry (Easton), 1992-08, Vol.31 (32), p.7373-7380

1992

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(E)-3-Cyanophosphoenolpyruvate, a new inhibitor of phosphoenolpyruvate-dependent enzymes

Biochemistry (Easton), 1985-12, Vol.24 (26), p.7602-7606

1985

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3-Hydroxy-3-methylglutaryl coenzyme A lyase: affinity labeling of the Pseudomonas mevalonii enzyme and assignment of cysteine-237 to the active site

Biochemistry (Easton), 1992-07, Vol.31 (29), p.6842-6847

1992

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3-Methyleneoxindole: An Affinity Label of Glutathione S-Transferase pi Which Targets Tryptophan 38

Biochemistry (Easton), 2001-06, Vol.40 (25), p.7549-7558

2001

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3-Phenylpropenes as mechanism-based inhibitors of dopamine .beta.-hydroxylase: evidence for a radical mechanism

Biochemistry (Easton), 1985-04, Vol.24 (9), p.2108-2114

1985

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3‘-Phosphoadenosine 5‘-Phosphosulfate Binding Site of Flavonol 3-Sulfotransferase Studied by Affinity Chromatography and 31P NMR

Biochemistry (Easton), 1999-03, Vol.38 (13), p.4066-4071

1999

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3-(Trifluoromethyl)-3-(m-[125I]iodophenyl)diazirine photolabels a substrate-binding site of rat hepatic cytochrome P-450 form PB-4

Biochemistry (Easton), 1986-08, Vol.25 (17), p.4797-4803

1986

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4-Bromotiglic Acid, a Novel Inhibitor of Thiolases and a Tool for Assessing the Cooperation between the Membrane-Bound and Soluble β-Oxidation Systems of Rat Liver Mitochondria

Biochemistry (Easton), 1998-11, Vol.37 (44), p.15548-15554

1998

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4′-Demethylnobiletin, a Bioactive Metabolite of Nobiletin Enhancing PKA/ERK/CREB Signaling, Rescues Learning Impairment Associated with NMDA Receptor Antagonism via Stimulation of the ERK Cascade

Biochemistry (Easton), 2009-08, Vol.48 (32), p.7713-7721

2009

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1.7 A structure of FR-1, a fibroblast growth factor-induced member of the aldo-keto reductase family, complexed with coenzyme and inhibitor

1-Aminocyclopropanephosphonate: time-dependent inactivation of 1-aminocyclopropanecarboxylate deaminase and Bacillus stearothermophilus alanine racemase by slow dissociation behavior

1-Ethynylpyrene, a suicide inhibitor of cytochrome P-450 dependent benzo[a]pyrene hydroxylase activity in liver microsomes

13C NMR study of the stereospecificity of the thiohemiacetals formed on inhibition of papain by specific enantiomeric aldehydes

15N NMR Relaxation Studies of Free and Inhibitor-Bound 4-Oxalocrotonate Tautomerase: Backbone Dynamics and Entropy Changes of an Enzyme upon Inhibitor Binding

15N NMR spectroscopy of hydrogen-bonding interactions in the active site of serine proteases: evidence for a moving histidine mechanism

18O isotopic 13C NMR shift as proof that bifunctional peptidylglycine α-amidating enzyme is a monooxygenase

19F NMR investigations of the catalytic mechanism of phosphoglucomutase using fluorinated substrates and inhibitors

(±)-(1S,2R,5S)-5-Amino-2-fluorocyclohex-3-enecarboxylic Acid. A Potent GABA Aminotransferase Inactivator that Irreversibly Inhibits via an Elimination−Aromatization Pathway

2,3-Diphosphoglycerate phosphatase activity of phosphoglycerate mutase: stimulation by vanadate and phosphate

2-[(4-Bromo-2,3-dioxobutyl)thio]adenosine 5'-monophosphate, a new nucleotide analog that acts as an affinity label of pyruvate kinase

2'-C-Methyladenosine and 2'-C-methyluridine 5'-diphosphates are mechanism-based inhibitors of ribonucleoside diphosphate reductase from Corynebacterium nephridii

2'-Deoxy-2'-halonucleotides as alternate substrates and mechanism-based inactivators of Lactobacillus leichmannii ribonucleotide reductase

2-Octynoyl coenzyme A is a mechanism-based inhibitor of pig kidney medium-chain acyl coenzyme A dehydrogenase: isolation of the target peptide

2-Oxo-3-alkynoic Acids, Universal Mechanism-Based Inactivators of Thiamin Diphosphate-Dependent Decarboxylases: Synthesis and Evidence for Potent Inactivation of the Pyruvate Dehydrogenase Multienzyme Complex

A 23-kDa protein as a substrate for protein kinase C in bovine neutrophils. Purification and partial characterization

A 3,4-dichloroisocoumarin-resistant component of the multicatalytic proteinase complex

(E)-3-Cyanophosphoenolpyruvate, a new inhibitor of phosphoenolpyruvate-dependent enzymes

3-Hydroxy-3-methylglutaryl coenzyme A lyase: affinity labeling of the Pseudomonas mevalonii enzyme and assignment of cysteine-237 to the active site

3-Methyleneoxindole: An Affinity Label of Glutathione S-Transferase pi Which Targets Tryptophan 38

3-Phenylpropenes as mechanism-based inhibitors of dopamine .beta.-hydroxylase: evidence for a radical mechanism

3‘-Phosphoadenosine 5‘-Phosphosulfate Binding Site of Flavonol 3-Sulfotransferase Studied by Affinity Chromatography and 31P NMR

3-(Trifluoromethyl)-3-(m-[125I]iodophenyl)diazirine photolabels a substrate-binding site of rat hepatic cytochrome P-450 form PB-4

4-Bromotiglic Acid, a Novel Inhibitor of Thiolases and a Tool for Assessing the Cooperation between the Membrane-Bound and Soluble β-Oxidation Systems of Rat Liver Mitochondria

4′-Demethylnobiletin, a Bioactive Metabolite of Nobiletin Enhancing PKA/ERK/CREB Signaling, Rescues Learning Impairment Associated with NMDA Receptor Antagonism via Stimulation of the ERK Cascade

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