AAAAAA

   
Results: 1-13 |
Results: 13
CATION-BINDING TO THE INTEGRIN CD11B I-DOMAIN AND ACTIVATION MODEL ASSESSMENT
Authors: BALDWIN ET SARVER RW BRYANT GL CURRY KA FAIRBANKS MB FINZEL BC GARLICK RL HEINRIKSON RL HORTON NC KELLEY LLC MILDNER AM MOON JB MOTT JE MUTCHLER VT TOMICH CSC WATENPAUGH KD WILEY VH
Citation: Et. Baldwin et al., CATION-BINDING TO THE INTEGRIN CD11B I-DOMAIN AND ACTIVATION MODEL ASSESSMENT, Structure, 6(7), 1998, pp. 923-935
STRUCTURAL CHARACTERIZATIONS OF NONPEPTIDIC THIADIAZOLE INHIBITORS OFMATRIX METALLOPROTEINASES REVEAL THE BASIS FOR STROMELYSIN SELECTIVITY
Authors: FINZEL BC BALDWIN ET BRYANT GL HESS GF WILKS JW TREPOD CM MOTT JE MARSHALL VP PETZOLD GL POORMAN RA OSULLIVAN TJ SCHOSTAREZ HJ MITCHELL MA
Citation: Bc. Finzel et al., STRUCTURAL CHARACTERIZATIONS OF NONPEPTIDIC THIADIAZOLE INHIBITORS OFMATRIX METALLOPROTEINASES REVEAL THE BASIS FOR STROMELYSIN SELECTIVITY, Protein science, 7(10), 1998, pp. 2118-2126
4-HYDROXY-5,6-DIHYDROPYRONES .2. POTENT NONPEPTIDE INHIBITORS OF HIV PROTEASE
Authors: TAIT BD HAGEN S DOMAGALA J ELLSWORTH EL GAJDA C HAMILTON HW PRASAD JVNV FERGUSON D GRAHAM N HUPE D NOUHAN C TUMMINO PJ HUMBLET C LUNNEY EA PAVLOVSKY A RUBIN J GRACHECK SJ BALDWIN ET BHAT TN ERICKSON JW GULNIK SV LIU BS
Citation: Bd. Tait et al., 4-HYDROXY-5,6-DIHYDROPYRONES .2. POTENT NONPEPTIDE INHIBITORS OF HIV PROTEASE, Journal of medicinal chemistry, 40(23), 1997, pp. 3781-3792
STRUCTURAL BASIS OF DRUG-RESISTANCE FOR THE V82A MUTANT OF HIV-1 PROTEINASE
Authors: BALDWIN ET BHAT TN LIU BS PATTABIRAMAN N ERICKSON JW
Citation: Et. Baldwin et al., STRUCTURAL BASIS OF DRUG-RESISTANCE FOR THE V82A MUTANT OF HIV-1 PROTEINASE, Nature structural biology, 2(3), 1995, pp. 244-249
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
NONPEPTIDIC POTENT HIV-1 PROTEASE INHIBITORS - -HYDROXY-6-PHENYL-2-OXO-2H-PYRAN-3-YL)THIOMETHANES THAT SPAN P-1-P-2' SUBSITES IN A UNIQUE MODE OF ACTIVE-SITE BINDING
Authors: PRASAD JVN PARA KS TUMMINO PJ FERGUSON D MCQUADE TJ LUNNEY EA RAPUNDALO ST BATLEY BL HINGORANI G DOMAGALA JM GRACHECK SJ BHAT TN LIU BS BALDWIN ET ERICKSON JW SAWYER TK
Citation: Jvn. Prasad et al., NONPEPTIDIC POTENT HIV-1 PROTEASE INHIBITORS - -HYDROXY-6-PHENYL-2-OXO-2H-PYRAN-3-YL)THIOMETHANES THAT SPAN P-1-P-2' SUBSITES IN A UNIQUE MODE OF ACTIVE-SITE BINDING, Journal of medicinal chemistry, 38(6), 1995, pp. 898-905
CRYSTAL-STRUCTURE OF A TETHERED DIMER OF HIV-1 PROTEINASE COMPLEXED WITH AND INHIBITOR
Authors: BHAT TN BALDWIN ET LIU BS CHENG YSE ERICKSON JW
Citation: Tn. Bhat et al., CRYSTAL-STRUCTURE OF A TETHERED DIMER OF HIV-1 PROTEINASE COMPLEXED WITH AND INHIBITOR, Nature structural biology, 1(8), 1994, pp. 552-556
STRUCTURAL-ANALYSIS OF THE SOLUBLE HUMAN UROKINASE-TYPE PLASMINOGEN-ACTIVATOR RECEPTOR (UPAR), AND ITS CONSTITUENT DOMAINS
Authors: CASASFINET JR PLOUG M BALDWIN ET DANO K ERICKSON JW
Citation: Jr. Casasfinet et al., STRUCTURAL-ANALYSIS OF THE SOLUBLE HUMAN UROKINASE-TYPE PLASMINOGEN-ACTIVATOR RECEPTOR (UPAR), AND ITS CONSTITUENT DOMAINS, The FASEB journal, 8(7), 1994, pp. 10001352-10001352
A NOVEL NONPEPTIDE HIV-1 PROTEASE INHIBITOR - ELUCIDATION OF THE BINDING MODE AND ITS APPLICATION IN THE DESIGN OF RELATED ANALOGS
Authors: LUNNEY EA HAGEN SE DOMAGALA JM HUMBLET C KOSINSKI J TAIT BD WARMUS JS WILSON M FERGUSON D HUPE D TUMMINO PJ BALDWIN ET BHAT TN LIU BS ERICKSON JW
Citation: Ea. Lunney et al., A NOVEL NONPEPTIDE HIV-1 PROTEASE INHIBITOR - ELUCIDATION OF THE BINDING MODE AND ITS APPLICATION IN THE DESIGN OF RELATED ANALOGS, Journal of medicinal chemistry, 37(17), 1994, pp. 2664-2677
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
NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS
Authors: PRASAD JVNV PARA KS LUNNEY EA ORTWINE DF DUNBAR JB FERGUSON D TUMMINO PJ HUPE D TAIT BD DOMAGALA JM HUMBLET C BHAT TN LIU BS GUERIN DMA BALDWIN ET ERICKSON JW SAWYER TK
Citation: Jvnv. Prasad et al., NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS, Journal of the American Chemical Society, 116(15), 1994, pp. 6989-6990
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
IDENTIFICATION OF A BINDING-SITE FOR THE HUMAN-IMMUNODEFICIENCY-VIRUSTYPE-1 NUCLEOCAPSID PROTEIN
Authors: SAKAGUCHI K ZAMBRANO N BALDWIN ET SHAPIRO BA ERICKSON JW OMICHINSKI JG CLORE GM GRONENBORN AM APPELLA E
Citation: K. Sakaguchi et al., IDENTIFICATION OF A BINDING-SITE FOR THE HUMAN-IMMUNODEFICIENCY-VIRUSTYPE-1 NUCLEOCAPSID PROTEIN, Proceedings of the National Academy of Sciences of the United Statesof America, 90(11), 1993, pp. 5219-5223
Risultati: 1-13 |