Search Results - "Betz, S F"
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1
Disulfide bonds and the stability of globular proteins
Published in Protein science (01-10-1993)“…An understanding of the forces that contribute to stability is pivotal in solving the protein‐folding problem. Classical theory suggests that disulfide bonds…”
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2
Discovery of Potent Antagonists of the Antiapoptotic Protein XIAP for the Treatment of Cancer
Published in Journal of medicinal chemistry (26-08-2004)“…Inhibitor of apoptosis (IAP) proteins are overexpressed in many cancers and have been implicated in tumor growth, pathogenesis, and resistance to chemo- or…”
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3
Structural basis for binding of Smac/DIABLO to the XIAP BIR3 domain
Published in Nature (London) (21-12-2000)“…The inhibitor-of-apoptosis proteins (IAPs) regulate programmed cell death by inhibiting members of the caspase family of enzymes. Recently, a mammalian protein…”
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4
The Crystal Structure of a Quercetin 2,3-Dioxygenase from Bacillus subtilis Suggests Modulation of Enzyme Activity by a Change in the Metal Ion at the Active Site(s)
Published in Biochemistry (Easton) (11-01-2005)“…Common structural motifs, such as the cupin domains, are found in enzymes performing different biochemical functions while retaining a similar active site…”
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5
Safety and Advantages of Bacillus thuringiensis-Protected Plants to Control Insect Pests
Published in Regulatory toxicology and pharmacology (01-10-2000)“…Plants modified to express insecticidal proteins from Bacillus thuringiensis (referred to as Bt-protected plants) provide a safe and highly effective method of…”
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6
Protein Design: A Hierarchic Approach
Published in Science (American Association for the Advancement of Science) (10-11-1995)“…The de novo design of peptides and proteins has recently emerged as an approach for investigating protein structure and function. Designed, helical peptides…”
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7
Introduction of a disulfide bond into cytochrome c stabilizes a compact denatured state
Published in Biochemistry (Easton) (15-12-1992)“…We introduced a novel disulfide bond, modeled on that of bullfrog cytochrome c, into yeast iso-1-cytochrome c. The disulfide spontaneously forms upon…”
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8
Amide proton exchange rates of oxidized and reduced saccharomyces cerevisiae iso‐1‐cytochrome c
Published in Protein science (01-11-1993)“…Proton NMR spectroscopy was used to determine the rate constant, kobs, for exchange of labile protons in both oxidized (Fe(III)) and reduced (Fe(II))…”
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9
Controlling Topology and Native-like Behavior of de Novo-Designed Peptides: Design and Characterization of Antiparallel Four-Stranded Coiled Coils
Published in Biochemistry (Easton) (28-05-1996)“…The de novo design of peptides and proteins has emerged as an attractive approach for investigating protein structure and function. Here, the design,…”
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10
De Novo Design of Native Proteins: Characterization of Proteins Intended To Fold into Antiparallel, Rop-like, Four-Helix Bundles
Published in Biochemistry (Easton) (04-03-1997)“…The de novo design and characterization of a series of 51-residue helix−turn−helix peptides intended to dimerize into antiparallel four-stranded coiled coils…”
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11
Probing weakly polar interactions in cytochrome c
Published in Protein science (01-12-1993)“…Theoretical, statistical, and model studies suggest that proteins are stabilized by weakly polar attractions between sulfur atoms and properly oriented…”
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12
Native-like and structurally characterized designed α-helical bundles
Published in Current opinion in structural biology (01-08-1995)“…A number of coiled coils and α-helical bundles have recently been designed, and many have now been structurally characterized by X-ray crystallography. Others…”
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13
Changes in global stability and local structure of cytochrome c upon substituting phenylalanine-82 with tyrosine
Published in Journal of inorganic biochemistry (15-08-1993)“…We have examined the F82Y;C102T variant of Saccharomyces cerevisiae iso-1-cytochrome c using high-resolution proton nuclear magnetic resonance spectroscopy,…”
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14
Hydrophobic Core Malleability of a De Novo Designed Three-helix Bundle Protein
Published in Journal of molecular biology (12-01-2001)“…De novo protein design provides a tool for testing the principles that stabilize the structures of proteins. Recently, we described the design and structure…”
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15
Function first: a powerful approach to post-genomic drug discovery
Published in Drug Discovery Today (15-08-2002)“…In the post-genomic era, pharmaceutical researchers must evaluate vast numbers of protein sequences and formulate novel, intelligent strategies for identifying…”
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9330 Atumelnant (crn04894) Induces Rapid And Sustained Reductions In Serum And Urine Cortisol In Patients With Acth-Dependent Cushing Syndrome During A Phase 1b/2a, Single Center, 10-day, Inpatient, Open-Label Study
Published in Journal of the Endocrine Society (05-10-2024)“…Disclosure: H. Elenius: Grant Recipient; Self; Crinetics Pharmaceuticals, Inc. R. McGlotten: Grant Recipient; Self; Crinetics Pharmaceuticals, Inc. C. Moore:…”
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17
Expression of de novo designed alpha-helical bundles
Published in Acta chemica Scandinavica (Copenhagen. 1989) (01-08-1996)“…The successful design of proteins requires careful consideration of the multiplicity of forces that stabilize their three-dimensional structures including…”
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18
Solution Structure of the Cytohesin-1 (B2-1) Sec7 Domain and Its Interaction with the GTPase ADP Ribosylation Factor 1
Published in Proceedings of the National Academy of Sciences - PNAS (07-07-1998)“…Cytohesin-1 (B2-1) is a guanine nucleotide exchange factor for human ADP ribosylation factor (Arf) GTPases, which are important for vesicular protein…”
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19
Unusual Effects of an Engineered Disulfide on Global and Local Protein Stability
Published in Biochemistry (Easton) (11-06-1996)“…The global and local stabilities of a eukaryotic ferricytochrome c variant with an engineered disulfide are examined. The disulfide connects position 20, which…”
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20
Protein thermal denaturation, side-chain models, and evolution: amino acid substitutions at a conserved helix-helix interface
Published in Biochemistry (Easton) (14-03-1995)“…Random mutant libraries with substitutions at the interface between the N- and C-terminal helices of Saccharomyces cerevisiae iso-1-cytochrome c were screened…”
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