1ta2
From Proteopedia
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[[Image:1ta2.png|left|200px]] | [[Image:1ta2.png|left|200px]] | ||
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==About this Structure== | ==About this Structure== | ||
| - | + | [[1ta2]] is a 2 chain structure of [[Hirudin]] 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=1TA2 OCA]. | |
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| + | ==See Also== | ||
| + | *[[Hirudin]] | ||
==Reference== | ==Reference== | ||
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[[Category: Vacca, J P.]] | [[Category: Vacca, J P.]] | ||
[[Category: Yan, Y.]] | [[Category: Yan, Y.]] | ||
| + | [[Category: Blood clotting]] | ||
| + | [[Category: Hydrolase/inhibitor complex]] | ||
[[Category: Thrombin inhibitor complex]] | [[Category: Thrombin inhibitor complex]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 23:32:00 2009'' | ||
Revision as of 23:44, 26 December 2010
Contents |
Crystal structure of thrombin in complex with compound 1
Template:ABSTRACT PUBMED 9703466
About this Structure
1ta2 is a 2 chain structure of Hirudin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Tucker TJ, Brady SF, Lumma WC, Lewis SD, Gardell SJ, Naylor-Olsen AM, Yan Y, Sisko JT, Stauffer KJ, Lucas BJ, Lynch JJ, Cook JJ, Stranieri MT, Holahan MA, Lyle EA, Baskin EP, Chen IW, Dancheck KB, Krueger JA, Cooper CM, Vacca JP. Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position. J Med Chem. 1998 Aug 13;41(17):3210-9. PMID:9703466 doi:http://dx.doi.org/10.1021/jm9801713
Categories: Homo sapiens | Thrombin | Baskin, E P. | Brady, S F. | Chen, I W. | Cook, J J. | Cooper, C M. | Dancheck, K B. | Gardel, S J. | Holahan, M A. | Krueger, J A. | Lewis, S D. | Lucas, B Y. | Lumma, W C. | Lyle, E A. | Lynch, J J. | Naylor-Olsen, A M. | Sisko, J T. | Stauffer, K J. | Stranieri, M T. | Tucker, T J. | Vacca, J P. | Yan, Y. | Blood clotting | Hydrolase/inhibitor complex | Thrombin inhibitor complex
