1ry7: Difference between revisions

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New page: left|200px<br /> <applet load="1ry7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ry7, resolution 3.20Å" /> '''Crystal Structure o...
 
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[[Image:1ry7.gif|left|200px]]<br />
[[Image:1ry7.gif|left|200px]]<br /><applet load="1ry7" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1ry7" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1ry7, resolution 3.20&Aring;" />
caption="1ry7, resolution 3.20&Aring;" />
'''Crystal Structure of the 3 Ig form of FGFR3c in complex with FGF1'''<br />
'''Crystal Structure of the 3 Ig form of FGFR3c in complex with FGF1'''<br />


==Overview==
==Overview==
The prototypical fibroblast growth factor receptor (FGFR) extracellular, domain consists of three Ig domains (D1-D3) of which the two, membrane-proximal D2 and D3 domains and the interconnecting D2-D3 linker, bear the determinants of ligand binding and specificity. In contrast, D1, and the D1-D2 linker are thought to play autoinhibitory roles in FGFR, regulation. Here, we report the crystal structure of the three-Ig form of, FGFR3c in complex with FGF1, an FGF that binds promiscuously to each of, the seven principal FGFRs. In this structure, D1 and the D1-D2 linker are, completely disordered, demonstrating that these regions are dispensable, for FGF binding. Real-time binding experiments using surface plasmon, resonance show that relative to two-Ig form, the three-Ig form of FGFR3c, exhibits lower affinity for both FGF1 and heparin. Importantly, we, demonstrate that this autoinhibition is mediated by intramolecular, interactions of D1 and the D1-D2 linker with the minimal FGF and, heparin-binding D2-D3 region. As in the FGF1-FGFR2c structure, but not the, FGF1-FGFR1c structure, the alternatively spliced betaC'-betaE loop is, ordered and interacts with FGF1 in the FGF1-FGFR3c structure. However, in, contrast to the FGF1-FGFR2c structure in which the betaC'-betaE loop, interacts with the beta-trefoil core region of FGF1, in the FGF1-FGFR3c, structure, this loop interacts extensively with the N-terminal region of, FGF1, underscoring the importance of the FGF1 N terminus in conferring, receptor-binding affinity and promiscuity. Importantly, comparison of the, three FGF1-FGFR structures shows that the flexibility of the betaC'-betaE, loop is a major determinant of ligand-binding specificity and promiscuity.
The prototypical fibroblast growth factor receptor (FGFR) extracellular domain consists of three Ig domains (D1-D3) of which the two membrane-proximal D2 and D3 domains and the interconnecting D2-D3 linker bear the determinants of ligand binding and specificity. In contrast, D1 and the D1-D2 linker are thought to play autoinhibitory roles in FGFR regulation. Here, we report the crystal structure of the three-Ig form of FGFR3c in complex with FGF1, an FGF that binds promiscuously to each of the seven principal FGFRs. In this structure, D1 and the D1-D2 linker are completely disordered, demonstrating that these regions are dispensable for FGF binding. Real-time binding experiments using surface plasmon resonance show that relative to two-Ig form, the three-Ig form of FGFR3c exhibits lower affinity for both FGF1 and heparin. Importantly, we demonstrate that this autoinhibition is mediated by intramolecular interactions of D1 and the D1-D2 linker with the minimal FGF and heparin-binding D2-D3 region. As in the FGF1-FGFR2c structure, but not the FGF1-FGFR1c structure, the alternatively spliced betaC'-betaE loop is ordered and interacts with FGF1 in the FGF1-FGFR3c structure. However, in contrast to the FGF1-FGFR2c structure in which the betaC'-betaE loop interacts with the beta-trefoil core region of FGF1, in the FGF1-FGFR3c structure, this loop interacts extensively with the N-terminal region of FGF1, underscoring the importance of the FGF1 N terminus in conferring receptor-binding affinity and promiscuity. Importantly, comparison of the three FGF1-FGFR structures shows that the flexibility of the betaC'-betaE loop is a major determinant of ligand-binding specificity and promiscuity.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1RY7 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1RY7 OCA].  
1RY7 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RY7 OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Basilico, C.]]
[[Category: Basilico, C.]]
[[Category: Eliseenkova, A.V.]]
[[Category: Eliseenkova, A V.]]
[[Category: Ibrahimi, O.A.]]
[[Category: Ibrahimi, O A.]]
[[Category: Linhardt, R.J.]]
[[Category: Linhardt, R J.]]
[[Category: Mohammadi, M.]]
[[Category: Mohammadi, M.]]
[[Category: Olsen, S.K.]]
[[Category: Olsen, S K.]]
[[Category: Raucci, A.]]
[[Category: Raucci, A.]]
[[Category: Schlessinger, J.]]
[[Category: Schlessinger, J.]]
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[[Category: fgf-fgfr complex; beta trefoil; ig domain]]
[[Category: fgf-fgfr complex; beta trefoil; ig domain]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 19:08:18 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:55:48 2008''