1gj7
From Proteopedia
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[[Image:1gj7.png|left|200px]] | [[Image:1gj7.png|left|200px]] | ||
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{{STRUCTURE_1gj7| PDB=1gj7 | SCENE= }} | {{STRUCTURE_1gj7| PDB=1gj7 | SCENE= }} | ||
===ENGINEERING INHIBITORS HIGHLY SELECTIVE FOR THE S1 SITES OF SER190 TRYPSIN-LIKE SERINE PROTEASE DRUG TARGETS=== | ===ENGINEERING INHIBITORS HIGHLY SELECTIVE FOR THE S1 SITES OF SER190 TRYPSIN-LIKE SERINE PROTEASE DRUG TARGETS=== | ||
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==See Also== | ==See Also== | ||
| - | *[[Urokinase]] | + | *[[Urokinase|Urokinase]] |
==Reference== | ==Reference== | ||
Revision as of 14:09, 26 July 2012
Contents |
ENGINEERING INHIBITORS HIGHLY SELECTIVE FOR THE S1 SITES OF SER190 TRYPSIN-LIKE SERINE PROTEASE DRUG TARGETS
Template:ABSTRACT PUBMED 11731301
About this Structure
1gj7 is a 2 chain structure of Urokinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Katz BA, Sprengeler PA, Luong C, Verner E, Elrod K, Kirtley M, Janc J, Spencer JR, Breitenbucher JG, Hui H, McGee D, Allen D, Martelli A, Mackman RL. Engineering inhibitors highly selective for the S1 sites of Ser190 trypsin-like serine protease drug targets. Chem Biol. 2001 Nov;8(11):1107-21. PMID:11731301
Categories: Homo sapiens | U-plasminogen activator | Allen, D. | Breitenbucher, J G. | Hui, H. | Katz, B A. | Luong, C. | Mackman, R L. | Martelli, A. | McGee, D. | Spencer, J R. | Sprengeler, P A. | Verner, E. | Blood clotting | H2o displacement | Hydrolase | Selectivity at s1 | Ser190/ala190 protease | Structure-based drug design | Tpa | Upa
