1gj7
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | {{Seed}} | ||
[[Image:1gj7.png|left|200px]] | [[Image:1gj7.png|left|200px]] | ||
| Line 20: | Line 19: | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1gj7]] is a 2 chain structure of [[Urokinase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1GJ7 OCA]. | |
| + | |||
| + | ==See Also== | ||
| + | *[[Urokinase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:011731301</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: U-plasminogen activator]] | [[Category: U-plasminogen activator]] | ||
| Line 37: | Line 39: | ||
[[Category: Sprengeler, P A.]] | [[Category: Sprengeler, P A.]] | ||
[[Category: Verner, E.]] | [[Category: Verner, E.]] | ||
| + | [[Category: Blood clotting]] | ||
[[Category: H2o displacement]] | [[Category: H2o displacement]] | ||
| + | [[Category: Hydrolase]] | ||
[[Category: Selectivity at s1]] | [[Category: Selectivity at s1]] | ||
[[Category: Ser190/ala190 protease]] | [[Category: Ser190/ala190 protease]] | ||
| Line 43: | Line 47: | ||
[[Category: Tpa]] | [[Category: Tpa]] | ||
[[Category: Upa]] | [[Category: Upa]] | ||
| - | |||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 10:26:18 2009'' | ||
Revision as of 09:45, 16 November 2011
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
