3bpr

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|PDB= 3bpr |SIZE=350|CAPTION= <scene name='initialview01'>3bpr</scene>, resolution 2.80&Aring;
|PDB= 3bpr |SIZE=350|CAPTION= <scene name='initialview01'>3bpr</scene>, resolution 2.80&Aring;
|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>
|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>
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|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>
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|LIGAND= <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=OLP:2-(2-HYDROXYETHYLAMINO)-6-(3-CHLOROANILINO)-9-ISOPROPYLPURINE'>OLP</scene>
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|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]
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|ACTIVITY= <span class='plainlinks'>[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] </span>
|GENE= MERTK, MER ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= MERTK, MER ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
 +
|DOMAIN=
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|RELATEDENTRY=[[2p0c|2P0C]], [[3brb|3BRB]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3bpr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3bpr OCA], [http://www.ebi.ac.uk/pdbsum/3bpr PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=3bpr RCSB]</span>
}}
}}
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[[Category: Walker, J R.]]
[[Category: Walker, J R.]]
[[Category: Weigelt, J.]]
[[Category: Weigelt, J.]]
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[[Category: CL]]
 
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[[Category: NA]]
 
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[[Category: OLP]]
 
[[Category: atp-binding]]
[[Category: atp-binding]]
[[Category: disease mutation]]
[[Category: disease mutation]]
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[[Category: vision]]
[[Category: vision]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 19:00:31 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 05:28:09 2008''

Revision as of 02:28, 31 March 2008

Image:3bpr.jpg


PDB ID 3bpr

Drag the structure with the mouse to rotate
, resolution 2.80Å
Sites: , , , , and
Ligands: , ,
Gene: MERTK, MER (Homo sapiens)
Activity: Receptor protein-tyrosine kinase, with EC number 2.7.10.1
Related: 2P0C, 3BRB


Resources: FirstGlance, OCA, PDBsum, RCSB
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 Mon Mar 31 05:28:09 2008

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