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=" | |||
caption="1ry7, resolution 3.20Å" /> | caption="1ry7, resolution 3.20Å" /> | ||
'''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 | 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:// | 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 | [[Category: Eliseenkova, A V.]] | ||
[[Category: Ibrahimi, O | [[Category: Ibrahimi, O A.]] | ||
[[Category: Linhardt, R | [[Category: Linhardt, R J.]] | ||
[[Category: Mohammadi, M.]] | [[Category: Mohammadi, M.]] | ||
[[Category: Olsen, S | [[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:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:55:48 2008'' | ||