Search Results - "DUNTEN, Pete"
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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
Published in The Journal of biological chemistry (16-07-2010)“…Heme is a vital molecule for all life forms with heme being capable of assisting in catalysis, binding ligands, and undergoing redox changes. Heme-related…”
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Structural Variations and Solvent Structure of r(UGGGGU) Quadruplexes Stabilized by Sr(2+) Ions
Published in Journal of molecular biology (19-06-2015)“…Guanine-rich sequences can, under appropriate conditions, adopt a distinctive, four-stranded, helical fold known as a G-quadruplex. Interest in quadruplex…”
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3
New paradigm for macromolecular crystallography experiments at SSRL: automated crystal screening and remote data collection
Published in Acta crystallographica. Section D, Biological crystallography. (01-12-2008)“…Complete automation of the macromolecular crystallography experiment has been achieved at SSRL through the combination of robust mechanized experimental…”
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4
Domain swapping in allosteric modulation of DNA specificity
Published in PLoS biology (01-12-2010)“…SgrAI is a type IIF restriction endonuclease that cuts an unusually long recognition sequence and exhibits allosteric self-modulation of cleavage activity and…”
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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
Published in Bioorganic & medicinal chemistry letters (15-07-2010)“…An analysis of the binding motifs of known HIV-1 non-nucleoside reverse transcriptase inhibitors has led to discovery of novel piperidine-linked…”
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6
Structure of an archaeal-type phosphoenolpyruvate carboxylase sensitive to inhibition by aspartate
Published in Proteins, structure, function, and bioinformatics (01-06-2011)“…The crystal structure of an archaeal‐type phosphoenolpyruvate carboxylase from Clostridium perfringens has been determined based on X‐ray data extending to 3…”
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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
Published in Acta crystallographica. Section D, Biological crystallography. (01-01-2011)“…SgrAI is a type II restriction endonuclease that cuts an unusually long recognition sequence and exhibits allosteric self‐activation with expansion of…”
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structure of SgrAI bound to DNA; recognition of an 8 base pair target
Published in Nucleic acids research (01-09-2008)“…The three-dimensional X-ray crystal structure of the 'rare cutting' type II restriction endonuclease SgrAI bound to cognate DNA is presented. SgrAI forms a…”
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X-ray Structure of a Hydroxylase−Regulatory Protein Complex from a Hydrocarbon-Oxidizing Multicomponent Monooxygenase, Pseudomonas sp. OX1 Phenol Hydroxylase
Published in Biochemistry (Easton) (26-12-2006)“…Phenol hydroxylase (PH) belongs to a family of bacterial multicomponent monooxygenases (BMMs) with carboxylate-bridged diiron active sites. Included are…”
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10
Structural Variations and Solvent Structure of r(UGGGGU) Quadruplexes Stabilized by Sr2+ Ions
Published in Journal of molecular biology (01-06-2015)“…Guanine-rich sequences can, under appropriate conditions, adopt a distinctive, four-stranded, helical fold known as a G-quadruplex. Interest in quadruplex…”
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11
Remote access to crystallography beamlines at SSRL: novel tools for training, education and collaboration
Published in Journal of applied crystallography (01-10-2010)“…For the past five years, the Structural Molecular Biology group at the Stanford Synchrotron Radiation Lightsource (SSRL) has provided general users of the…”
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12
Insights into the Structure and Regulation of Glucokinase from a Novel Mutation (V62M), Which Causes Maturity-onset Diabetes of the Young
Published in The Journal of biological chemistry (08-04-2005)“…Glucokinase (GCK) serves as the pancreatic glucose sensor. Heterozygous inactivating GCK mutations cause hyperglycemia, whereas activating mutations cause…”
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13
Crystal structure of human cytosolic phosphoenolpyruvate carboxykinase reveals a new GTP-binding site
Published in Journal of molecular biology (15-02-2002)“…We report crystal structures of the human enzyme phosphoenolpyruvate carboxykinase (PEPCK) with and without bound substrates. These structures are the first to…”
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14
The restriction enzyme SgrAI: structure solution via combination of poor MIRAS and MR phases
Published in Acta crystallographica. Section D, Biological crystallography. (01-04-2009)“…Uninterpretable electron‐density maps were obtained using either MIRAS phases or MR phases in attempts to determine the structure of the type II restriction…”
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15
Expression, purification and crystallization of an archaeal-type phosphoenolpyruvate carboxylase
Published in Acta crystallographica. Section F, Structural biology and crystallization communications (01-11-2009)“…An archaeal‐type phosphoenolpyruvate carboxylase (PepcA) from Clostridium perfringens has been expressed in Escherichia coli in a soluble form with an…”
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Structural insights into sGC activation by different activators
Published in BMC pharmacology (01-08-2011)Get full text
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Crystal structure of the dipeptide binding protein from Escherichia coli involved in active transport and chemotaxis
Published in Protein science (01-11-1995)“…The Escherichia coli periplasmic dipeptide binding protein functions in both peptide transport and taxis toward peptides. The structure of the dipeptide…”
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Mutations That Affect Ligand Binding to the Escherichia coli Aspartate Receptor
Published in The Journal of biological chemistry (26-01-2001)“…Three arginine residues of the binding site of the Escherichia coli aspartate receptor contribute to its high affinity for aspartate (Kd ∼3 μm). Site-directed…”
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Structure and specificity of FEN-1 from Methanopyrus kandleri
Published in Proteins, structure, function, and bioinformatics (01-01-2015)“…ABSTRACT DNA repair is fundamental to genome stability and is found in all three domains of life. However many archaeal species, such as Methanopyrus kandleri,…”
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20
Discovery of potent and bioavailable GSK-3β inhibitors
Published in Bioorganic & medicinal chemistry letters (01-03-2010)“…A series of maleimides was discovered with high potency and good selectivity for GSK-3β. The most potent compound 34 has an IC 50 of 0.6 nM for GSK-3β, over…”
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