2gs2

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[[Image:2gs2.gif|left|200px]]
[[Image:2gs2.gif|left|200px]]
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{{Structure
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|PDB= 2gs2 |SIZE=350|CAPTION= <scene name='initialview01'>2gs2</scene>, resolution 2.800&Aring;
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The line below this paragraph, containing "STRUCTURE_2gs2", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND=
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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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>
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or leave the SCENE parameter empty for the default display.
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|GENE= EGFR ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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|DOMAIN=
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{{STRUCTURE_2gs2| PDB=2gs2 | SCENE= }}
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|RELATEDENTRY=[[2gs6|2GS6]], [[2gs7|2GS7]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2gs2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2gs2 OCA], [http://www.ebi.ac.uk/pdbsum/2gs2 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2gs2 RCSB]</span>
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'''Crystal Structure of the active EGFR kinase domain'''
'''Crystal Structure of the active EGFR kinase domain'''
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[[Category: Shen, K.]]
[[Category: Shen, K.]]
[[Category: Zhang, X.]]
[[Category: Zhang, X.]]
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[[Category: active]]
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[[Category: Active]]
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[[Category: egfr]]
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[[Category: Egfr]]
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[[Category: kinase]]
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[[Category: Kinase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 05:27:10 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:20:47 2008''
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Revision as of 02:27, 4 May 2008

Template:STRUCTURE 2gs2

Crystal Structure of the active EGFR kinase domain


Contents

Overview

The mechanism by which the epidermal growth factor receptor (EGFR) is activated upon dimerization has eluded definition. We find that the EGFR kinase domain can be activated by increasing its local concentration or by mutating a leucine (L834R) in the activation loop, the phosphorylation of which is not required for activation. This suggests that the kinase domain is intrinsically autoinhibited, and an intermolecular interaction promotes its activation. Using further mutational analysis and crystallography we demonstrate that the autoinhibited conformation of the EGFR kinase domain resembles that of Src and cyclin-dependent kinases (CDKs). EGFR activation results from the formation of an asymmetric dimer in which the C-terminal lobe of one kinase domain plays a role analogous to that of cyclin in activated CDK/cyclin complexes. The CDK/cyclin-like complex formed by two kinase domains thus explains the activation of EGFR-family receptors by homo- or heterodimerization.

Disease

Known disease associated with this structure: Adenocarcinoma of lung, response to tyrosine kinase inhibitor in OMIM:[131550], Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in OMIM:[131550], Nonsmall cell lung cancer, susceptibility to OMIM:[131550]

About this Structure

2GS2 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

An allosteric mechanism for activation of the kinase domain of epidermal growth factor receptor., Zhang X, Gureasko J, Shen K, Cole PA, Kuriyan J, Cell. 2006 Jun 16;125(6):1137-49. PMID:16777603 Page seeded by OCA on Sun May 4 05:27:10 2008

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