1bx8: Difference between revisions
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[[Image:1bx8.jpg|left|200px]] | [[Image:1bx8.jpg|left|200px]] | ||
'''HIRUSTASIN FROM HIRUDO MEDICINALIS AT 1.4 ANGSTROMS''' | {{Structure | ||
|PDB= 1bx8 |SIZE=350|CAPTION= <scene name='initialview01'>1bx8</scene>, resolution 1.40Å | |||
|SITE= | |||
|LIGAND= <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene> | |||
|ACTIVITY= | |||
|GENE= | |||
}} | |||
'''HIRUSTASIN FROM HIRUDO MEDICINALIS AT 1.4 ANGSTROMS''' | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
1BX8 is a [ | 1BX8 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Hirudo_medicinalis Hirudo medicinalis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BX8 OCA]. | ||
==Reference== | ==Reference== | ||
The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitors., Uson I, Sheldrick GM, de La Fortelle E, Bricogne G, Di Marco S, Priestle JP, Grutter MG, Mittl PR, Structure. 1999 Jan 15;7(1):55-63. PMID:[http:// | The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitors., Uson I, Sheldrick GM, de La Fortelle E, Bricogne G, Di Marco S, Priestle JP, Grutter MG, Mittl PR, Structure. 1999 Jan 15;7(1):55-63. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10368273 10368273] | ||
[[Category: Hirudo medicinalis]] | [[Category: Hirudo medicinalis]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: anti-coagulant]] | [[Category: anti-coagulant]] | ||
[[Category: conformational flexibility]] | [[Category: conformational flexibility]] | ||
[[Category: peptidic | [[Category: peptidic inhibitor]] | ||
[[Category: serine protease inhibitor]] | [[Category: serine protease inhibitor]] | ||
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