2bm2
From Proteopedia
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{{STRUCTURE_2bm2| PDB=2bm2 | SCENE= }} | {{STRUCTURE_2bm2| PDB=2bm2 | SCENE= }} | ||
===HUMAN BETA-II TRYPTASE IN COMPLEX WITH 4-(3-AMINOMETHYL-PHENYL)-PIPERIDIN-1-YL-(5-PHENETHYL- PYRIDIN-3-YL)-METHANONE=== | ===HUMAN BETA-II TRYPTASE IN COMPLEX WITH 4-(3-AMINOMETHYL-PHENYL)-PIPERIDIN-1-YL-(5-PHENETHYL- PYRIDIN-3-YL)-METHANONE=== | ||
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==About this Structure== | ==About this Structure== | ||
| - | + | [[2bm2]] is a 4 chain structure of [[Tryptase]] 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=2BM2 OCA]. | |
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| + | ==See Also== | ||
| + | *[[Tryptase|Tryptase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015781396</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Tryptase]] | [[Category: Tryptase]] | ||
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[[Category: Glycoprotein]] | [[Category: Glycoprotein]] | ||
[[Category: Hydrolase]] | [[Category: Hydrolase]] | ||
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[[Category: Protease]] | [[Category: Protease]] | ||
[[Category: Serine protease]] | [[Category: Serine protease]] | ||
[[Category: Serine protease inhibitor]] | [[Category: Serine protease inhibitor]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 06:21:41 2009'' | ||
Revision as of 09:14, 26 July 2012
Contents |
HUMAN BETA-II TRYPTASE IN COMPLEX WITH 4-(3-AMINOMETHYL-PHENYL)-PIPERIDIN-1-YL-(5-PHENETHYL- PYRIDIN-3-YL)-METHANONE
Template:ABSTRACT PUBMED 15781396
About this Structure
2bm2 is a 4 chain structure of Tryptase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Levell J, Astles P, Eastwood P, Cairns J, Houille O, Aldous S, Merriman G, Whiteley B, Pribish J, Czekaj M, Liang G, Maignan S, Guilloteau JP, Dupuy A, Davidson J, Harrison T, Morley A, Watson S, Fenton G, McCarthy C, Romano J, Mathew R, Engers D, Gardyan M, Sides K, Kwong J, Tsay J, Rebello S, Shen L, Wang J, Luo Y, Giardino O, Lim HK, Smith K, Pauls H. Structure based design of 4-(3-aminomethylphenyl)piperidinyl-1-amides: novel, potent, selective, and orally bioavailable inhibitors of betaII tryptase. Bioorg Med Chem. 2005 Apr 15;13(8):2859-72. PMID:15781396 doi:10.1016/j.bmc.2005.02.014
Categories: Homo sapiens | Tryptase | Aldous, S. | Astles, P. | Cairns, J. | Czekaj, M. | Davidson, J. | Dupuy, A. | Eastwood, P. | Engers, D. | Fenton, G. | Gardyan, M. | Giardino, O. | Guilloteau, J P. | Harrison, T. | Houille, O. | Kwong, J. | Levell, J. | Liang, G. | Lim, H K. | Luo, Y. | Maignan, S. | Mathew, R. | Mccarthy, C. | Merriman, G. | Morley, A. | Pauls, H. | Pribish, J. | Rebello, S. | Romano, J. | Shen, L. | Sides, K. | Smith, K. | Tsay, J. | Wang, J. | Watson, S. | Whiteley, B. | Glycoprotein | Hydrolase | Protease | Serine protease | Serine protease inhibitor
