| 1c5o |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
19.3 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5p |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.2 |
62.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c5q |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.2 |
55.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5r |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.1 |
53.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c5s |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.4 |
58.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c5t |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.2 |
53.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5u |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.2 |
52.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5v |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
17.2 |
55.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5w |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
18.5 |
63.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5x |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
18.5 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5y |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
18.5 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1c5z |
STRUCTURAL BASIS FOR SELECTIVITY OF A SMALL MOLECULE, S1-BINDING, SUB-MICROMOLAR INHIBITOR OF UROKINASE TYPE PLASMINOGEN ACTIVATOR |
18.6 |
64.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c60 |
T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM ARGON |
17.5 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1c61 |
T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM KRYPTON |
17.4 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1c62 |
T4 LYSOZYME MUTANT C54T/C97A/F153A IN THE PRESENCE OF 8 ATM XENON |
17.3 |
61.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1c63 |
T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM ARGON |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1c64 |
T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM KRYPTON |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1c65 |
T4 LYSOZYME MUTANT C54T/C97A/L121A IN THE PRESENCE OF 8 ATM XENON |
17.4 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1c66 |
T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM ARGON |
17.4 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1c67 |
T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM KRYPTON |
17.3 |
60.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1c68 |
T4 LYSOZYME MUTANT C54T/C97A/L121A/L133A IN THE PRESENCE OF 8 ATM XENON |
17.2 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1c69 |
T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM ARGON |
17.5 |
61.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6a |
T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM KRYPTON |
17.4 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6b |
T4 LYSOZYME MUTANT C54T/C97A/L133A IN THE PRESENCE OF 8 ATM XENON |
17.4 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6c |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 16 ATM ARGON |
17.4 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6d |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 16 ATM KRYPTON |
17.4 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6e |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 2 ATM XENON |
17.2 |
57.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c6f |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 32 ATM ARGON |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6g |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 4 ATM KRYPTON |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6h |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 4 ATM XENON |
17.2 |
58.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c6i |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM ARGON |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6j |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM KRYPTON |
17.3 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6k |
T4 LYSOZYME MUTANT C54T/C97A/L99A IN THE PRESENCE OF 8 ATM XENON |
17.2 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6l |
T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM ARGON |
17.5 |
59.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c6m |
T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM KRYPTON |
17.3 |
62.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6n |
T4 LYSOZYME MUTANT C54T/C97A/L99A/F153A IN THE PRESENCE OF 8 ATM XENON |
17.2 |
60.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6o |
CRYSTAL STRUCTURE OF OXIDIZED CYTOCHROME C6 FROM THE GREEN ALGAE SCENEDESMUS OBLIQUUS |
18.8 |
62.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6p |
T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM ARGON |
17.6 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6q |
T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM KRYPTON |
17.4 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6r |
CRYSTAL STRUCTURE OF REDUCED CYTOCHROME C6 FROM THE GREEN ALGAE SCENEDESMUS OBLIQUUS |
13.2 |
38.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1c6s |
THE SOLUTION STRUCTURE OF CYTOCHROME C6 FROM THE THERMOPHILIC CYANOBACTERIUM SYNECHOCOCCUS ELONGATUS, NMR, 20 STRUCTURES |
11.4 |
35.3 |
SOLUTION NMR |
GOOD
|
| 1c6t |
T4 LYSOZYME MUTANT C54T/C97A IN THE PRESENCE OF 8 ATM XENON |
17.4 |
58.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c6v |
SIV INTEGRASE (CATALYTIC DOMAIN + DNA BIDING DOMAIN COMPRISING RESIDUES 50-293) MUTANT WITH PHE 185 REPLACED BY HIS (F185H) |
30.1 |
95.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1c6w |
MAUROCALCIN FROM SCORPIO MAURUS |
15.4 |
57.4 |
SOLUTION NMR |
GOOD
|
| 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.
; |
18.3 |
60.5 |
X-RAY DIFFRACTION |
GOOD
|
| 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.
; |
18.5 |
64.3 |
X-RAY DIFFRACTION |
GOOD
|
| 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.
; |
18.2 |
65.0 |
X-RAY DIFFRACTION |
GOOD
|
| 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.
; |
18.3 |
63.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1c72 |
;TYR115, GLN165 AND TRP209 CONTRIBUTE TO THE 1,2-EPOXY-3-(P-NITROPHENOXY)PROPANE CONJUGATING ACTIVITIES OF GLUTATHIONE S-TRANSFERASE CGSTM1-1
; |
35.1 |
115.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1c74 |
Structure of the double mutant (K53,56M) of phospholipase A2 |
15.4 |
54.4 |
X-RAY DIFFRACTION |
GOOD
|