2pzr

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{{STRUCTURE_2pzr| PDB=2pzr | SCENE= }}
{{STRUCTURE_2pzr| PDB=2pzr | SCENE= }}
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'''Crystal Strucure of FGF Receptor 2 (FGFR2) Kinase Domain Harboring the Pathogenic K641R Mutation Responsible for Pfeiffer Syndrome'''
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===Crystal Strucure of FGF Receptor 2 (FGFR2) Kinase Domain Harboring the Pathogenic K641R Mutation Responsible for Pfeiffer Syndrome===
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==Overview==
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Activating mutations in the tyrosine kinase domain of receptor tyrosine kinases (RTKs) cause cancer and skeletal disorders. Comparison of the crystal structures of unphosphorylated and phosphorylated wild-type FGFR2 kinase domains with those of seven unphosphorylated pathogenic mutants reveals an autoinhibitory "molecular brake" mediated by a triad of residues in the kinase hinge region of all FGFRs. Structural analysis shows that many other RTKs, including PDGFRs, VEGFRs, KIT, CSF1R, FLT3, TEK, and TIE, are also subject to regulation by this brake. Pathogenic mutations activate FGFRs and other RTKs by disengaging the brake either directly or indirectly.
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(as it appears on PubMed at http://www.pubmed.gov), where 17803937 is the PubMed ID number.
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{{ABSTRACT_PUBMED_17803937}}
==About this Structure==
==About this Structure==
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[[Category: Kinase domain fold consisting of n- and c-lobe]]
[[Category: Kinase domain fold consisting of n- and c-lobe]]
[[Category: Transferase]]
[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 14:04:49 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 19:58:17 2008''

Revision as of 16:58, 27 July 2008

Image:2pzr.png

Template:STRUCTURE 2pzr

Crystal Strucure of FGF Receptor 2 (FGFR2) Kinase Domain Harboring the Pathogenic K641R Mutation Responsible for Pfeiffer Syndrome

Template:ABSTRACT PUBMED 17803937

About this Structure

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

Reference

A molecular brake in the kinase hinge region regulates the activity of receptor tyrosine kinases., Chen H, Ma J, Li W, Eliseenkova AV, Xu C, Neubert TA, Miller WT, Mohammadi M, Mol Cell. 2007 Sep 7;27(5):717-30. PMID:17803937

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