Authors:
VILENCHIK LZ
GRIFFITH JP
STCLAIR N
NAVIA MA
MARGOLIN AL
Citation: Lz. Vilenchik et al., PROTEIN CRYSTALS AS NOVEL MICROPOROUS MATERIALS, Journal of the American Chemical Society, 120(18), 1998, pp. 4290-4294
Citation: Ma. Navia, PROTEIN-DRUG COMPLEXES IMPORTANT FOR IMMUNOREGULATION AND ORGAN-TRANSPLANTATION, Current opinion in structural biology, 6(6), 1996, pp. 838-847
Citation: S. Itoh et Ma. Navia, STRUCTURE COMPARISON OF NATIVE AND MUTANT HUMAN RECOMBINANT FKBP12 COMPLEXES WITH THE IMMUNOSUPPRESSANT DRUG FK506 (TACROLIMUS), Protein science, 4(11), 1995, pp. 2261-2268
Authors:
ITOH S
DECENZO MT
LIVINGSTON DJ
PEARLMAN DA
NAVIA MA
Citation: S. Itoh et al., CONFORMATION OF FK506 IN X-RAY STRUCTURES OF ITS COMPLEXES WITH HUMANRECOMBINANT FKBP12 MUTANTS, Bioorganic & medicinal chemistry letters, 5(17), 1995, pp. 1983-1988
Authors:
WILSON KP
YAMASHITA MM
SINTCHAK MD
ROTSTEIN SH
MURCKO MA
BOGER J
THOMSON JA
FITZGIBBON MJ
BLACK JR
NAVIA MA
Citation: Kp. Wilson et al., COMPARATIVE X-RAY STRUCTURES OF THE MAJOR BINDING-PROTEIN FOR THE IMMUNOSUPPRESSANT FK506 (TACROLIMUS) IN UNLIGANDED FORM AND IN COMPLEX WITH FK506 AND RAPAMYCIN, Acta crystallographica. Section D, Biological crystallography, 51, 1995, pp. 511-521
Authors:
ARMISTEAD DM
BADIA MC
DEININGER DD
DUFFY JP
SAUNDERS JO
TUNG RD
THOMSON JA
DECENZO MT
FUTER O
LIVINGSTON DJ
MURCKO MA
YAMASHITA MM
NAVIA MA
Citation: Dm. Armistead et al., DESIGN, SYNTHESIS AND STRUCTURE OF NON-MACROCYCLIC INHIBITORS OF FKBP12, THE MAJOR BINDING-PROTEIN FOR THE IMMUNOSUPPRESSANT FK506, Acta crystallographica. Section D, Biological crystallography, 51, 1995, pp. 522-528
Authors:
GRIFFITH JP
KIM JL
KIM EE
SINTCHAK MD
THOMSON JA
FITZGIBBON MJ
FLEMING MA
CARON PR
HSIAO K
NAVIA MA
Citation: Jp. Griffith et al., X-RAY STRUCTURE OF CALCINEURIN INHIBITED BY THE IMMUNOPHILIN IMMUNOSUPPRESSANT FKBP12-FK506 COMPLEX, Cell, 82(3), 1995, pp. 507-522
Authors:
KIM EE
BAKER CT
DWYER MD
MURCKO MA
RAO BG
TUNG RD
NAVIA MA
Citation: Ee. Kim et al., CRYSTAL-STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH VX-478, A POTENT AND ORALLY BIOAVAILABLE INHIBITOR OF THE ENZYME, Journal of the American Chemical Society, 117(3), 1995, pp. 1181-1182
Authors:
PERSICHETTI RA
STCLAIR NL
GRIFFITH JP
NAVIA MA
MARGOLIN AL
Citation: Ra. Persichetti et al., CROSS-LINKED ENZYME CRYSTALS (CLECS) OF THERMOLYSIN IN THE SYNTHESIS OF PEPTIDES, Journal of the American Chemical Society, 117(10), 1995, pp. 2732-2737
Authors:
CONNELLY PR
ALDAPE RA
BRUZZESE FJ
CHAMBERS SP
FITZGIBBON MJ
FLEMING MA
ITOH S
LIVINGSTON DJ
NAVIA MA
THOMSON JA
WILSON KP
Citation: Pr. Connelly et al., ENTHALPY OF HYDROGEN-BOND FORMATION IN A PROTEIN-LIGAND BINDING REACTION, Proceedings of the National Academy of Sciences of the United Statesof America, 91(5), 1994, pp. 1964-1968
Citation: S. Itoh et al., PRELIMINARY-ANALYSIS OF MULTIPLE CRYSTAL FORMS OF THE BOVINE CYCLOPHILIN CYCLOSPORINE-A COMPLEX, Journal of Molecular Biology, 235(3), 1994, pp. 1136-1140
Authors:
DELUCAS LJ
LONG MM
MOORE KM
ROSENBLUM WM
BRAY TL
SMITH C
CARSON M
NARAYANA SVL
HARRINGTON MD
CARTER D
CLARK AD
NANNI RG
DING J
JACOBOMOLINA A
KAMER G
HUGHES SH
ARNOLD E
EINSPAHR HM
CLANCY LL
RAO GSJ
COOK PF
HARRIS BG
MUNSON SH
FINZEL BC
MCPHERSON A
WEBER PC
LEWANDOWSKI FA
NAGABHUSHAN TL
TROTTA PP
REICHERT P
NAVIA MA
WILSON KP
THOMSON JA
RICHARDS RN
BOWERSOX KD
MEADE CJ
BAKER ES
BISHOP SP
DUNBAR BJ
TRINH E
PRAHL J
SACCO A
BUGG CE
Citation: Lj. Delucas et al., RECENT RESULTS AND NEW HARDWARE DEVELOPMENTS FOR PROTEIN CRYSTAL-GROWTH IN MICROGRAVITY, Journal of crystal growth, 135(1-2), 1994, pp. 183-195
Citation: Ma. Navia et Da. Peattie, STRUCTURE-BASED DRUG DESIGN - APPLICATIONS IN IMMUNOPHARMACOLOGY AND IMMUNOSUPPRESSION, Trends in pharmacological sciences, 14(5), 1993, pp. 189-195
Citation: Ma. Navia et Da. Peattie, STRUCTURE-BASED DRUG DESIGN - APPLICATIONS IN IMMUNOPHARMACOLOGY AND IMMUNOSUPPRESSION, Immunology today, 14(6), 1993, pp. 296-302