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Results: 1-10 |
Results: 10
ANALYSIS OF INTRACELLULAR TRAFFICKING AND INTERACTIONS OF CYTOPLASMICHIV-1 REV MUTANTS IN LIVING CELLS
Authors: STAUBER RH AFONINA E GULNIK S ERICKSON J PAVLAKIS GN
Citation: Rh. Stauber et al., ANALYSIS OF INTRACELLULAR TRAFFICKING AND INTERACTIONS OF CYTOPLASMICHIV-1 REV MUTANTS IN LIVING CELLS, Virology (New York, N.Y. Print), 251(1), 1998, pp. 38-48
A METHOD MEASURING STEADY-STATE KINETIC CONSTANTS OF CHEMICALLY UNMODIFIED PEPTIDE - APPLICATION TO STUDY OF HIV PROTEINASE
Authors: SUVOROV L XIE D GULNIK S ERICKSON J
Citation: L. Suvorov et al., A METHOD MEASURING STEADY-STATE KINETIC CONSTANTS OF CHEMICALLY UNMODIFIED PEPTIDE - APPLICATION TO STUDY OF HIV PROTEINASE, The FASEB journal, 11(9), 1997, pp. 3143-3143
DISSECTION OF THE PH-DEPENDENCE OF INHIBITOR BINDING ENERGETICS FOR AN ASPARTIC PROTEASE - DIRECT MEASUREMENT OF THE PROTONATION STATES OF THE CATALYTIC ASPARTIC-ACID RESIDUES
Authors: XIE D GULNIK S COLLINS L GUSTCHINA E SUVOROV L ERICKSON JW
Citation: D. Xie et al., DISSECTION OF THE PH-DEPENDENCE OF INHIBITOR BINDING ENERGETICS FOR AN ASPARTIC PROTEASE - DIRECT MEASUREMENT OF THE PROTONATION STATES OF THE CATALYTIC ASPARTIC-ACID RESIDUES, Biochemistry, 36(51), 1997, pp. 16166-16172
NEW SERIES OF POTENT, ORALLY BIOAVAILABLE, NONPEPTIDIC CYCLIC SULFONES AS HIV-1 PROTEASE INHIBITORS
Authors: KIM CU MCGEE LR KRAWCZYK SH HARWOOD E HARADA Y SWAMINATHAN S BISCHOFBERGER N CHEN MS CHERRINGTON JM XIONG SF GRIFFIN L CUNDY KC LEE A YU B GULNIK S ERICKSON JW
Citation: Cu. Kim et al., NEW SERIES OF POTENT, ORALLY BIOAVAILABLE, NONPEPTIDIC CYCLIC SULFONES AS HIV-1 PROTEASE INHIBITORS, Journal of medicinal chemistry, 39(18), 1996, pp. 3431-3434
STRUCTURAL MECHANISMS OF DRUG-RESISTANCE FOR HIV-1 PROTEASE MUTANTS
Authors: ERICKSON JW BHAT TN MUNSHI S GULNIK S
Citation: Jw. Erickson et al., STRUCTURAL MECHANISMS OF DRUG-RESISTANCE FOR HIV-1 PROTEASE MUTANTS, Journal of acquired immune deficiency syndromes and human retrovirology, 10, 1995, pp. 63-63
STRUCTURE OF HIV-1 PROTEASE WITH KNI-272, A TIGHT-BINDING TRANSITION-STATE ANALOG CONTAINING ALLOPHENYLNORSTATINE
Authors: BALDWIN ET BHAT TN GULNIK S LIU BS TOPOL IA KISO Y MIMOTO T MITSUYA H ERICKSON JW
Citation: Et. Baldwin et al., STRUCTURE OF HIV-1 PROTEASE WITH KNI-272, A TIGHT-BINDING TRANSITION-STATE ANALOG CONTAINING ALLOPHENYLNORSTATINE, Structure, 3(6), 1995, pp. 581-590
BINDING OF HIV PROTEASE TO AN IMMOBILIZED INHIBITOR - A REAL-TIME KINETIC-STUDY UTILIZING SURFACE-PLASMON RESONANCE
Authors: FISHER RJ FIVASH M BLADEN S GULNIK S MAJHER P LAUTENBERGER J ERICKSON J
Citation: Rj. Fisher et al., BINDING OF HIV PROTEASE TO AN IMMOBILIZED INHIBITOR - A REAL-TIME KINETIC-STUDY UTILIZING SURFACE-PLASMON RESONANCE, AIDS research and human retroviruses, 11, 1995, pp. 161-161
BINDING-STUDIES OF HIV-1 REV PROTEIN AND PEPTIDES TO RRE SEQUENCES
Authors: CASASFINET JR AFONINA E GULNIK S ADACHI Y PAVLAKIS GN ERICKSON JW
Citation: Jr. Casasfinet et al., BINDING-STUDIES OF HIV-1 REV PROTEIN AND PEPTIDES TO RRE SEQUENCES, Biophysical journal, 66(2), 1994, pp. 10000358-10000358
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C(2) SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE
Authors: HOSUR MV BHAT TN KEMPF DJ BALDWIN ET LIU BS GULNIK S WIDEBURG NE NORBECK DW APPELT K ERICKSON JW
Citation: Mv. Hosur et al., INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C(2) SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE, Journal of the American Chemical Society, 116(3), 1994, pp. 847-855
CRYSTAL-STRUCTURES OF NATIVE AND INHIBITED FORMS OF HUMAN CATHEPSIN-D- IMPLICATIONS FOR LYSOSOMAL TARGETING AND DRUG DESIGN
Authors: BALDWIN ET BHAT TN GULNIK S HOSUR MV SOWDER RC CACHAU RE COLLINS J SILVA AM ERICKSON JW
Citation: Et. Baldwin et al., CRYSTAL-STRUCTURES OF NATIVE AND INHIBITED FORMS OF HUMAN CATHEPSIN-D- IMPLICATIONS FOR LYSOSOMAL TARGETING AND DRUG DESIGN, Proceedings of the National Academy of Sciences of the United Statesof America, 90(14), 1993, pp. 6796-6800
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