2jbp: Difference between revisions
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[[Image:2jbp.jpg|left|200px]] | [[Image:2jbp.jpg|left|200px]] | ||
'''PROTEIN KINASE MK2 IN COMPLEX WITH AN INHIBITOR (CRYSTAL FORM-2, CO-CRYSTALLIZATION)''' | {{Structure | ||
|PDB= 2jbp |SIZE=350|CAPTION= <scene name='initialview01'>2jbp</scene>, resolution 3.31Å | |||
|SITE= <scene name='pdbsite=AC1:P4o+Binding+Site+For+Chain+A'>AC1</scene>, <scene name='pdbsite=AC2:P4o+Binding+Site+For+Chain+B'>AC2</scene>, <scene name='pdbsite=AC3:P4o+Binding+Site+For+Chain+C'>AC3</scene>, <scene name='pdbsite=AC4:P4o+Binding+Site+For+Chain+D'>AC4</scene>, <scene name='pdbsite=AC5:P4o+Binding+Site+For+Chain+E'>AC5</scene>, <scene name='pdbsite=AC6:P4o+Binding+Site+For+Chain+F'>AC6</scene>, <scene name='pdbsite=AC7:P4o+Binding+Site+For+Chain+G'>AC7</scene>, <scene name='pdbsite=AC8:P4o+Binding+Site+For+Chain+H'>AC8</scene>, <scene name='pdbsite=AC9:P4o+Binding+Site+For+Chain+I'>AC9</scene>, <scene name='pdbsite=BC1:P4o+Binding+Site+For+Chain+K'>BC1</scene> and <scene name='pdbsite=BC2:P4o+Binding+Site+For+Chain+L'>BC2</scene> | |||
|LIGAND= <scene name='pdbligand=P4O:2-(2-QUINOLIN-3-YLPYRIDIN-4-YL)-1,5,6,7-TETRAHYDRO-4H-PYRROLO[3,2-C]PYRIDIN-4-ONE'>P4O</scene> | |||
|ACTIVITY= [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] | |||
|GENE= | |||
}} | |||
'''PROTEIN KINASE MK2 IN COMPLEX WITH AN INHIBITOR (CRYSTAL FORM-2, CO-CRYSTALLIZATION)''' | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
2JBP is a [ | 2JBP is a [[Single protein]] structure of 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=2JBP OCA]. | ||
==Reference== | ==Reference== | ||
Structural basis for a high affinity inhibitor bound to protein kinase MK2., Hillig RC, Eberspaecher U, Monteclaro F, Huber M, Nguyen D, Mengel A, Muller-Tiemann B, Egner U, J Mol Biol. 2007 Jun 8;369(3):735-45. Epub 2007 Mar 12. PMID:[http:// | Structural basis for a high affinity inhibitor bound to protein kinase MK2., Hillig RC, Eberspaecher U, Monteclaro F, Huber M, Nguyen D, Mengel A, Muller-Tiemann B, Egner U, J Mol Biol. 2007 Jun 8;369(3):735-45. Epub 2007 Mar 12. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17449059 17449059] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: transferase]] | [[Category: transferase]] | ||
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