2pvy
From Proteopedia
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{{STRUCTURE_2pvy| PDB=2pvy | SCENE= }} | {{STRUCTURE_2pvy| PDB=2pvy | SCENE= }} | ||
| - | + | ===Crystal Strucure of FGF Receptor 2 (FGFR2) Kinase Domain Harboring the Pathogenic K659N Mutation Responsible for an Unclassified Craniosynostosis Syndrome.=== | |
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| - | + | The line below this paragraph, {{ABSTRACT_PUBMED_17803937}}, adds the Publication Abstract to the page | |
| + | (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]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 07:57:47 2008'' | ||
Revision as of 04:57, 28 July 2008
Crystal Strucure of FGF Receptor 2 (FGFR2) Kinase Domain Harboring the Pathogenic K659N Mutation Responsible for an Unclassified Craniosynostosis Syndrome.
Template:ABSTRACT PUBMED 17803937
About this Structure
2PVY 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
Page seeded by OCA on Mon Jul 28 07:57:47 2008
