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3FCS

Structure of complete ectodomain of integrin aIIBb3

Summary for 3FCS
Entry DOI10.2210/pdb3fcs/pdb
Related3FCU
DescriptorIntegrin, alpha 2b, MAGNESIUM ION, Integrin beta-3, ... (11 entities in total)
Functional Keywordsbeta propeller, rossmann fold, egf domain, cell adhesion, disease mutation, glycoprotein, host-virus interaction, integrin, membrane, phosphoprotein, receptor, transmembrane, cell adhesion-immune system complex, cell adhesion-blood clotting complex, cell adhesion/blood clotting
Biological sourceHomo sapiens (human)
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Total number of polymer chains4
Total formula weight368902.43
Authors
Zhu, J.,Luo, B.-H.,Xiao, T.,Zhang, C.,Nishida, N.,Springer, T.A. (deposition date: 2008-11-22, release date: 2009-01-20, Last modification date: 2024-10-16)
Primary citationZhu, J.,Luo, B.H.,Xiao, T.,Zhang, C.,Nishida, N.,Springer, T.A.
Structure of a complete integrin ectodomain in a physiologic resting state and activation and deactivation by applied forces.
Mol.Cell, 32:849-861, 2008
Cited by
PubMed Abstract: The complete ectodomain of integrin alpha(IIb)beta(3) reveals a bent, closed, low-affinity conformation, the beta knee, and a mechanism for linking cytoskeleton attachment to high affinity for ligand. Ca and Mg ions in the recognition site, including the synergistic metal ion binding site (SyMBS), are loaded prior to ligand binding. Electrophilicity of the ligand-binding Mg ion is increased in the open conformation. The beta(3) knee passes between the beta(3)-PSI and alpha(IIb)-knob to bury the lower beta leg in a cleft, from which it is released for extension. Different integrin molecules in crystals and EM reveal breathing that appears on pathway to extension. Tensile force applied to the extended ligand-receptor complex stabilizes the closed, low-affinity conformation. By contrast, an additional lateral force applied to the beta subunit to mimic attachment to moving actin filaments stabilizes the open, high-affinity conformation. This mechanism propagates allostery over long distances and couples cytoskeleton attachment of integrins to their high-affinity state.
PubMed: 19111664
DOI: 10.1016/j.molcel.2008.11.018
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.55 Å)
Structure validation

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数据于2024-10-30公开中

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