3bpr
From Proteopedia
(Difference between revisions)
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| - | [[Image:3bpr.jpg|left|200px]] | + | [[Image:3bpr.jpg|left|200px]] |
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| - | '''Crystal structure of catalytic domain of the proto-oncogene tyrosine-protein kinase MER in complex with inhibitor C52''' | + | {{Structure |
| + | |PDB= 3bpr |SIZE=350|CAPTION= <scene name='initialview01'>3bpr</scene>, resolution 2.80Å | ||
| + | |SITE= <scene name='pdbsite=AC1:Na+Binding+Site+For+Residue+B+1'>AC1</scene>, <scene name='pdbsite=AC2:Cl+Binding+Site+For+Residue+C+133'>AC2</scene>, <scene name='pdbsite=AC3:Olp+Binding+Site+For+Residue+A+900'>AC3</scene>, <scene name='pdbsite=AC4:Olp+Binding+Site+For+Residue+B+900'>AC4</scene>, <scene name='pdbsite=AC5:Olp+Binding+Site+For+Residue+C+900'>AC5</scene> and <scene name='pdbsite=AC6:Olp+Binding+Site+For+Residue+D+900'>AC6</scene> | ||
| + | |LIGAND= <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene> and <scene name='pdbligand=OLP:2-(2-HYDROXYETHYLAMINO)-6-(3-CHLOROANILINO)-9-ISOPROPYLPURINE'>OLP</scene> | ||
| + | |ACTIVITY= [http://en.wikipedia.org/wiki/Receptor_protein-tyrosine_kinase Receptor protein-tyrosine kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 2.7.10.1] | ||
| + | |GENE= MERTK, MER ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
| + | }} | ||
| + | |||
| + | '''Crystal structure of catalytic domain of the proto-oncogene tyrosine-protein kinase MER in complex with inhibitor C52''' | ||
| + | |||
==About this Structure== | ==About this Structure== | ||
| - | 3BPR is a [ | + | 3BPR 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=3BPR OCA]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Receptor protein-tyrosine kinase]] | [[Category: Receptor protein-tyrosine kinase]] | ||
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[[Category: sgc]] | [[Category: sgc]] | ||
[[Category: signal]] | [[Category: signal]] | ||
| - | [[Category: structural | + | [[Category: structural genomic]] |
[[Category: structural genomics consortium]] | [[Category: structural genomics consortium]] | ||
[[Category: transferase]] | [[Category: transferase]] | ||
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[[Category: vision]] | [[Category: vision]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 19:00:31 2008'' |
Revision as of 17:00, 20 March 2008
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| , resolution 2.80Å | |||||||
|---|---|---|---|---|---|---|---|
| Sites: | , , , , and | ||||||
| Ligands: | , and | ||||||
| Gene: | MERTK, MER (Homo sapiens) | ||||||
| Activity: | Receptor protein-tyrosine kinase, with EC number 2.7.10.1 | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Crystal structure of catalytic domain of the proto-oncogene tyrosine-protein kinase MER in complex with inhibitor C52
About this Structure
3BPR is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Mar 20 19:00:31 2008
Categories: Homo sapiens | Receptor protein-tyrosine kinase | Single protein | Arrowsmith, C H. | Bochkarev, A. | Dhe-Paganon, S. | Edwards, A M. | Huang, X. | Jr, P J.Finerty. | SGC, Structural Genomics Consortium. | Walker, J R. | Weigelt, J. | CL | NA | OLP | Atp-binding | Disease mutation | Glycoprotein | Immunoglobulin domain | Kinase | Membrane | Nucleotide-binding | Phosphoprotein | Phosphorylation | Polymorphism | Proto-oncogene | Receptor | Retinitis pigmentosa | Sensory transduction | Sgc | Signal | Structural genomic | Structural genomics consortium | Transferase | Transmembrane | Tyrosine-protein kinase | Vision
