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Proline inhibits aggregation during protein refolding
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- 01 February 2000, pp. 344-352
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Homology modeling and molecular dynamics simulations of lymphotactin
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- 15 December 2000, pp. 2192-2199
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Modeling of loops in protein structures
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- 05 October 2000, pp. 1753-1773
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Peptide and metal ion-dependent association of isolated helix-loop-helix calcium binding domains: Studies of thrombic fragments of calmodulin
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- 01 May 2000, pp. 964-975
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HYR, an extracellular module involved in cellular adhesion and related to the immunoglobulin-like fold
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- 01 July 2000, pp. 1382-1390
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New insight on β-lactoglobulin binding sites by 1-anilinonaphthalene-8-sulfonate fluorescence decay
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- 15 December 2000, pp. 1968-1974
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Fluorinated alcohol, the third group of cosolvents that stabilize the molten-globule state relative to a highly denatured state of cytochrome c
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- 01 March 2000, pp. 564-569
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Improving protein crystal quality by decoupling nucleation and growth in vapor diffusion
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- 01 April 2000, pp. 755-757
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Alternative modes of binding of proteins with tandem SH2 domains
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- 01 March 2000, pp. 570-579
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Amino acid repeat patterns in protein sequences: Their diversity and structural-functional implications
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- 01 June 2000, pp. 1203-1209
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Structure of a protein G helix variant suggests the importance of helix propensity and helix dipole interactions in protein design
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- 01 July 2000, pp. 1391-1394
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Three-dimensional model of the extracellular domain of the type 4a metabotropic glutamate receptor: New insights into the activation process
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- 15 December 2000, pp. 2200-2209
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Structural and functional consequences of removal of the interdomain disulfide bridge from the isolated C-lobe of ovotransferrin
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- 01 August 2000, pp. 1567-1575
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Antibody-detected folding: Kinetics of surface epitope formation are distinct from other folding phases
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- 01 January 2000, pp. 129-137
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Substrate- and pH-dependent contribution of oxyanion binding site to the catalysis of prolyl oligopeptidase, a paradigm of the serine oligopeptidase family
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- 01 February 2000, pp. 353-360
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Specificity in substrate binding by protein folding catalysts: Tyrosine and tryptophan residues are the recognition motifs for the binding of peptides to the pancreas-specific protein disulfide isomerase PDIp
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- 01 April 2000, pp. 758-764
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Comparison of binding energies of SrcSH2-phosphotyrosyl peptides with structure-based prediction using surface area based empirical parameterization
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- 15 December 2000, pp. 1975-1985
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The oxidation produced by hydrogen peroxide on Ca-ATP-G-actin
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- 05 October 2000, pp. 1774-1782
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NMR solution structure of Apis mellifera chymotrypsin/cathepsin G inhibitor-1 (AMCI-1): Structural similarity with Ascaris protease inhibitors
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- 01 May 2000, pp. 976-984
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Thermal stability of Clostridium pasteurianum rubredoxin: Deconvoluting the contributions of the metal site and the protein
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- 10 February 2001, pp. 2413-2426
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