1iil: Difference between revisions

New page: left|200px<br /> <applet load="1iil" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iil, resolution 2.3Å" /> '''CRYSTAL STRUCTURE OF...
 
No edit summary
Line 1: Line 1:
[[Image:1iil.gif|left|200px]]<br />
[[Image:1iil.gif|left|200px]]<br /><applet load="1iil" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1iil" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1iil, resolution 2.3&Aring;" />
caption="1iil, resolution 2.3&Aring;" />
'''CRYSTAL STRUCTURE OF PRO253ARG APERT MUTANT FGF RECEPTOR 2 (FGFR2) IN COMPLEX WITH FGF2'''<br />
'''CRYSTAL STRUCTURE OF PRO253ARG APERT MUTANT FGF RECEPTOR 2 (FGFR2) IN COMPLEX WITH FGF2'''<br />


==Overview==
==Overview==
Apert syndrome (AS) is characterized by craniosynostosis (premature fusion, of cranial sutures) and severe syndactyly of the hands and feet. Two, activating mutations, Ser-252 --&gt; Trp and Pro-253 --&gt; Arg, in fibroblast, growth factor receptor 2 (FGFR2) account for nearly all known cases of AS., To elucidate the mechanism by which these substitutions cause AS, we, determined the crystal structures of these two FGFR2 mutants in complex, with fibroblast growth factor 2 (FGF2). These structures demonstrate that, both mutations introduce additional interactions between FGFR2 and FGF2, thereby augmenting FGFR2-FGF2 affinity. Moreover, based on these, structures and sequence alignment of the FGF family, we propose that the, Pro-253 --&gt; Arg mutation will indiscriminately increase the affinity of, FGFR2 toward any FGF. In contrast, the Ser-252 --&gt; Trp mutation will, selectively enhance the affinity of FGFR2 toward a limited subset of FGFs., These predictions are consistent with previous biochemical data describing, the effects of AS mutations on FGF binding. Alterations in FGFR2 ligand, affinity and specificity may allow inappropriate autocrine or paracrine, activation of FGFR2. Furthermore, the distinct gain-of-function, interactions observed in each crystal structure provide a model to explain, the phenotypic variability among AS patients.
Apert syndrome (AS) is characterized by craniosynostosis (premature fusion of cranial sutures) and severe syndactyly of the hands and feet. Two activating mutations, Ser-252 --&gt; Trp and Pro-253 --&gt; Arg, in fibroblast growth factor receptor 2 (FGFR2) account for nearly all known cases of AS. To elucidate the mechanism by which these substitutions cause AS, we determined the crystal structures of these two FGFR2 mutants in complex with fibroblast growth factor 2 (FGF2). These structures demonstrate that both mutations introduce additional interactions between FGFR2 and FGF2, thereby augmenting FGFR2-FGF2 affinity. Moreover, based on these structures and sequence alignment of the FGF family, we propose that the Pro-253 --&gt; Arg mutation will indiscriminately increase the affinity of FGFR2 toward any FGF. In contrast, the Ser-252 --&gt; Trp mutation will selectively enhance the affinity of FGFR2 toward a limited subset of FGFs. These predictions are consistent with previous biochemical data describing the effects of AS mutations on FGF binding. Alterations in FGFR2 ligand affinity and specificity may allow inappropriate autocrine or paracrine activation of FGFR2. Furthermore, the distinct gain-of-function interactions observed in each crystal structure provide a model to explain the phenotypic variability among AS patients.


==Disease==
==Disease==
Line 11: Line 10:


==About this Structure==
==About this Structure==
1IIL is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IIL OCA].  
1IIL is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IIL OCA].  


==Reference==
==Reference==
Line 18: Line 17:
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Transferase]]
[[Category: Transferase]]
[[Category: Eliseenkova, A.V.]]
[[Category: Eliseenkova, A V.]]
[[Category: Ibrahimi, O.A.]]
[[Category: Ibrahimi, O A.]]
[[Category: Mohammadi, M.]]
[[Category: Mohammadi, M.]]
[[Category: Ornitz, D.M.]]
[[Category: Ornitz, D M.]]
[[Category: Plotnikov, A.N.]]
[[Category: Plotnikov, A N.]]
[[Category: b-trefoil]]
[[Category: b-trefoil]]
[[Category: immunoglobulin like domain]]
[[Category: immunoglobulin like domain]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:30:18 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:12:15 2008''

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA