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Domain swapping in allosteric modulation of DNA specificity

PLoS biology, 2010-12, Vol.8 (12), p.e1000554-e1000554

2010

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Structure of Cinaciguat (BAY 58–2667) Bound to Nostoc H-NOX Domain Reveals Insights into Heme-mimetic Activation of the Soluble Guanylyl Cyclase

The Journal of biological chemistry, 2010-07, Vol.285 (29), p.22651-22657

2010

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Structural Variations and Solvent Structure of r(UGGGGU) Quadruplexes Stabilized by Sr(2+) Ions

Journal of molecular biology, 2015-06, Vol.427 (12), p.2205-2219

2015

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Structural Variations and Solvent Structure of r(UGGGGU) Quadruplexes Stabilized by Sr2+ Ions

Journal of molecular biology, 2015-06, Vol.427 (12), p.2205-2219

2015

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Discovery of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Benzyl derivatives with broad potency against resistant mutant viruses

Bioorganic & medicinal chemistry letters, 2010-07, Vol.20 (14), p.4215-4218

2010

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Structure of an archaeal-type phosphoenolpyruvate carboxylase sensitive to inhibition by aspartate

Proteins, structure, function, and bioinformatics, 2011-06, Vol.79 (6), p.1820-1829

2011

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New clues in the allosteric activation of DNA cleavage by SgrAI: structures of SgrAI bound to cleaved primary-site DNA and uncleaved secondary-site DNA

Acta crystallographica. Section D, Biological crystallography., 2011-01, Vol.67 (1), p.67-74

2011

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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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The structure of SgrAI bound to DNA; recognition of an 8 base pair target

Nucleic acids research, 2008-09, Vol.36 (16), p.5405

2008

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Remote access to crystallography beamlines at SSRL: novel tools for training, education and collaboration

Journal of applied crystallography, 2010-10, Vol.43 (5-2), p.1261-1270

2010

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The restriction enzyme SgrAI: structure solution via combination of poor MIRAS and MR phases

Acta crystallographica. Section D, Biological crystallography., 2009-04, Vol.65 (4), p.393-398

2009

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Expression, purification and crystallization of an archaeal-type phosphoenolpyruvate carboxylase

Acta crystallographica. Section F, Structural biology and crystallization communications, 2009-11, Vol.65 (11), p.1193-1196

2009

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Domain Swapping in Allosteric Modulation of DNA Specificity: e1000554

PLoS biology, 2010-12, Vol.8 (12)

2010

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Structural insights into sGC activation by different activators

BMC pharmacology, 2011-08, Vol.11 (S1), p.O11-O11, Article O11

2011

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New clues in the allosteric activation of DNA cleavage by Sgr AI: structures of Sgr AI bound to cleaved primary-site DNA and uncleaved secondary-site DNA

Acta crystallographica. Section D, Biological crystallography., 2011-01, Vol.67 (1), p.67-74

2011

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The restriction enzyme Sgr AI: structure solution via combination of poor MIRAS and MR phases

Acta crystallographica. Section D, Biological crystallography., 2009-04, Vol.65 (4), p.393-398

2009

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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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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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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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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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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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Domain swapping in allosteric modulation of DNA specificity

Structure of Cinaciguat (BAY 58–2667) Bound to Nostoc H-NOX Domain Reveals Insights into Heme-mimetic Activation of the Soluble Guanylyl Cyclase

Structural Variations and Solvent Structure of r(UGGGGU) Quadruplexes Stabilized by Sr(2+) Ions

Structural Variations and Solvent Structure of r(UGGGGU) Quadruplexes Stabilized by Sr2+ Ions

Discovery of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Benzyl derivatives with broad potency against resistant mutant viruses

Structure of an archaeal-type phosphoenolpyruvate carboxylase sensitive to inhibition by aspartate

New clues in the allosteric activation of DNA cleavage by SgrAI: structures of SgrAI bound to cleaved primary-site DNA and uncleaved secondary-site DNA

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

The structure of SgrAI bound to DNA; recognition of an 8 base pair target

Remote access to crystallography beamlines at SSRL: novel tools for training, education and collaboration

The restriction enzyme SgrAI: structure solution via combination of poor MIRAS and MR phases

Expression, purification and crystallization of an archaeal-type phosphoenolpyruvate carboxylase

Domain Swapping in Allosteric Modulation of DNA Specificity: e1000554

Structural insights into sGC activation by different activators

New clues in the allosteric activation of DNA cleavage by Sgr AI: structures of Sgr AI bound to cleaved primary-site DNA and uncleaved secondary-site DNA

The restriction enzyme Sgr AI: structure solution via combination of poor MIRAS and MR phases

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

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

A new series of potent oxindole inhibitors of CDK2

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

A New Series of Potent Oxindole Inhibitors of CDK2

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