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Crystal structure of human cytosolic phosphoenolpyruvate carboxykinase reveals a new GTP-binding site

Journal of molecular biology, 2002-02, Vol.316 (2), p.257-264

2002

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X‐ray structure of a novel matrix metalloproteinase inhibitor complexed to stromelysin

Protein science, 2001-05, Vol.10 (5), p.923-926

2001

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Delineating the activity of the potent nicotinic acetylcholine receptor agonists (+)‐anatoxin‐a and (−)‐hosieine‐A

Acta crystallographica. Section F, Structural biology communications, 2022-09, Vol.78 (9), p.313-323

2022

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Crystal structure of the dipeptide binding protein from Escherichia coli involved in active transport and chemotaxis

Protein science, 1995-11, Vol.4 (11), p.2327-2334

1995

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X-ray Structure of a Hydroxylase−Regulatory Protein Complex from a Hydrocarbon-Oxidizing Multicomponent Monooxygenase, Pseudomonas sp. OX1 Phenol Hydroxylase

Biochemistry (Easton), 2006-12, Vol.45 (51), p.15392-15404

2006

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Insights into the Structure and Regulation of Glucokinase from a Novel Mutation (V62M), Which Causes Maturity-onset Diabetes of the Young

The Journal of biological chemistry, 2005-04, Vol.280 (14), p.14105-14113

2005

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Tuning the responsiveness of a sensory receptor via covalent modification

The Journal of biological chemistry, 1991-01, Vol.266 (3), p.1491-1496

1991

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Design and Synthesis of 4-Azaindoles as Inhibitors of p38 MAP Kinase

Journal of medicinal chemistry, 2003-10, Vol.46 (22), p.4702-4713

2003

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Expression, characterization and structure determination of an active site mutant (Glu202–Gln) of mini-stromelysin-1

Protein engineering, 2000-06, Vol.13 (6), p.397-405

2000

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Modeling of the structure of the Haemophilus influenzae heme‐binding protein suggests a mode of heme interaction

Protein science, 1995-11, Vol.4 (11), p.2335-2340

1995

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A new series of potent oxindole inhibitors of CDK2

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.913-917

2004

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Protein Farnesyltransferase: Structure and Implications for Substrate Binding

Biochemistry (Easton), 1998-06, Vol.37 (22), p.7907-7912

1998

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Crystallization and Preliminary X-ray Analysis of the Periplasmic Dipeptide Binding Protein from Escherichia coli

Journal of molecular biology, 1993-05, Vol.231 (1), p.145-147

1993

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Novel 5,5-disubstitutedpyrimidine-2,4,6-triones as selective MMP inhibitors

Bioorganic & medicinal chemistry letters, 2001-04, Vol.11 (8), p.969-972

2001

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C-8 Modifications of 3-alkyl-1,8-dibenzylxanthines as inhibitors of human cytosolic phosphoenolpyruvate carboxykinase

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (14), p.3835-3839

2007

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Modified 3-alkyl-1,8-dibenzylxanthines as GTP-competitive inhibitors of phosphoenolpyruvate carboxykinase

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (20), p.3607-3610

2003

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X-ray structures of two xanthine inhibitors bound to PEPCK and N-3 modifications of substituted 1,8-dibenzylxanthines

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (21), p.3871-3874

2003

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Locating non-crystallographic symmetry elements: the program FIND 2 FOLDS

Acta crystallographica. Section A, Foundations of crystallography, 2002-08, Vol.58 (s1), p.c76-c76

2002

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Mutations that affect ligand binding to the Escherichia coli aspartate receptor: implications for transmembrane signaling

The Journal of biological chemistry, 2001-01, Vol.276 (4), p.2808-2815

2001

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Remote access and automation at SSRL

Acta crystallographica. Section A, Foundations of crystallography, 2011-08, Vol.67 (a1), p.C45-C46

2011

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A New Series of Potent Oxindole Inhibitors of CDK2

Bioorganic & medicinal chemistry, 2004-06, Vol.35 (25), p.no-no

2004

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New Paradigm for Macromolecular Crystallography Experiments at SSRL: Automated Crystal Screening And Remote Data Collection

Acta crystallographica. Section D, Biological crystallography., 2009-05, Vol.64 (Pt12)

2009

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Protein Farnesyltransferase: Structure and Implications for Substrate Binding

Biochemistry (Easton), 1998-09, Vol.37 (37), p.13042-13042

1998

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Crystallization of 5-keto-4-deoxyuronate isomerase from Escherichia coli

Acta crystallographica. Section D, Biological crystallography., 1998-07, Vol.54 (4), p.678-680

1998

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Site-directed alkylation and the alternating access model for LacY

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (2), p.491-494

2007

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Crystal structure of human cytosolic phosphoenolpyruvate carboxykinase reveals a new GTP-binding site

X‐ray structure of a novel matrix metalloproteinase inhibitor complexed to stromelysin

Delineating the activity of the potent nicotinic acetylcholine receptor agonists (+)‐anatoxin‐a and (−)‐hosieine‐A

Crystal structure of the dipeptide binding protein from Escherichia coli involved in active transport and chemotaxis

X-ray Structure of a Hydroxylase−Regulatory Protein Complex from a Hydrocarbon-Oxidizing Multicomponent Monooxygenase, Pseudomonas sp. OX1 Phenol Hydroxylase

Insights into the Structure and Regulation of Glucokinase from a Novel Mutation (V62M), Which Causes Maturity-onset Diabetes of the Young

Tuning the responsiveness of a sensory receptor via covalent modification

Design and Synthesis of 4-Azaindoles as Inhibitors of p38 MAP Kinase

Expression, characterization and structure determination of an active site mutant (Glu202–Gln) of mini-stromelysin-1

Modeling of the structure of the Haemophilus influenzae heme‐binding protein suggests a mode of heme interaction

A new series of potent oxindole inhibitors of CDK2

Protein Farnesyltransferase: Structure and Implications for Substrate Binding

Crystallization and Preliminary X-ray Analysis of the Periplasmic Dipeptide Binding Protein from Escherichia coli

Novel 5,5-disubstitutedpyrimidine-2,4,6-triones as selective MMP inhibitors

C-8 Modifications of 3-alkyl-1,8-dibenzylxanthines as inhibitors of human cytosolic phosphoenolpyruvate carboxykinase

Modified 3-alkyl-1,8-dibenzylxanthines as GTP-competitive inhibitors of phosphoenolpyruvate carboxykinase

X-ray structures of two xanthine inhibitors bound to PEPCK and N-3 modifications of substituted 1,8-dibenzylxanthines

Locating non-crystallographic symmetry elements: the program FIND 2 FOLDS

Mutations that affect ligand binding to the Escherichia coli aspartate receptor: implications for transmembrane signaling

Remote access and automation at SSRL

A New Series of Potent Oxindole Inhibitors of CDK2

New Paradigm for Macromolecular Crystallography Experiments at SSRL: Automated Crystal Screening And Remote Data Collection

Protein Farnesyltransferase: Structure and Implications for Substrate Binding

Crystallization of 5-keto-4-deoxyuronate isomerase from Escherichia coli

Site-directed alkylation and the alternating access model for LacY

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