| 1c5o |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5p |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5q |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5r |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5s |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5t |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5u |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5v |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5w |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5x |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5y |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c5z |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
1 |
1 |
X-RAY DIFFRACTION |
| 1c60 |
T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c61 |
T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c62 |
T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c63 |
T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c64 |
T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c65 |
T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c66 |
T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c67 |
T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c68 |
T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c69 |
T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6a |
T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6b |
T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6c |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 16 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6d |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 16 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6e |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 2 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6f |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 32 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6g |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 4 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6h |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 4 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6i |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6j |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6k |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6l |
T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6m |
T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6n |
T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6o |
CRYSTAL STRUCTURE OF OXIDIZED CYTOCHROME C6 FROM THE GREEN ALGAE SCENEDESMUS OBLIQUUS |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6p |
T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM ARGON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6q |
T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM KRYPTON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6r |
CRYSTAL STRUCTURE OF REDUCED CYTOCHROME C6 FROM THE GREEN ALGAE SCENEDESMUS OBLIQUUS |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6s |
THE SOLUTION STRUCTURE OF CYTOCHROME C6 FROM THE THERMOPHILIC CYANOBACTERIUM SYNECHOCOCCUS ELONGATUS, NMR, 20 STRUCTURES |
20 |
20 |
SOLUTION NMR |
| 1c6t |
T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM XENON |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6v |
SIV INTEGRASE (CATALYTIC DOMAIN + DNA BIDING DOMAIN COMPRISING RESIDUES 50-293) MUTANT WITH PHE 185 REPLACED BY HIS (F185H) |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6w |
MAUROCALCIN FROM SCORPIO MAURUS |
25 |
25 |
SOLUTION NMR |
| 1c6x |
ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6y |
ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
1 |
1 |
X-RAY DIFFRACTION |
| 1c6z |
ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
1 |
1 |
X-RAY DIFFRACTION |
| 1c70 |
ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP. |
1 |
1 |
X-RAY DIFFRACTION |
| 1c72 |
TYR115, GLN165 AND TRP209 CONTRIBUTE TO THE 1,2-EPOXY-3-(P-NITROPHENOXY)PROPANE CONJUGATING ACTIVITIES OF GLUTATHIONE S-TRANSFERASE CGSTM1-1 |
2 |
2 |
X-RAY DIFFRACTION |
| 1c74 |
Structure of the double mutant (K53,56M) of phospholipase A2 |
1 |
1 |
X-RAY DIFFRACTION |