1t0p: Difference between revisions

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[[Image:1t0p.gif|left|200px]]
{{Seed}}
[[Image:1t0p.png|left|200px]]


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{{STRUCTURE_1t0p|  PDB=1t0p  |  SCENE=  }}  
{{STRUCTURE_1t0p|  PDB=1t0p  |  SCENE=  }}  


'''Structural Basis of ICAM recognition by integrin alpahLbeta2 revealed in the complex structure of binding domains of ICAM-3 and alphaLbeta2 at 1.65 A'''
===Structural Basis of ICAM recognition by integrin alpahLbeta2 revealed in the complex structure of binding domains of ICAM-3 and alphaLbeta2 at 1.65 A===




==Overview==
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Within the Ig superfamily (IgSF), intercellular adhesion molecules (ICAMs) form a subfamily that binds the leukocyte integrin alphaLbeta2. We report a 1.65-A-resolution crystal structure of the ICAM-3 N-terminal domain (D1) in complex with the inserted domain, the ligand-binding domain of alphaLbeta2. This high-resolution structure and comparisons among ICAM subfamily members establish that the binding of ICAM-3 D1 onto the inserted domain represents a common docking mode for ICAM subfamily members. The markedly different off-rates of ICAM-1, -2, and -3 appear to be determined by the hydrophobicity of residues that surround a metal coordination bond in the alphaLbeta2-binding interfaces. Variation in composition of glycans on the periphery of the interfaces influences on-rate.
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{{ABSTRACT_PUBMED_15728350}}


==About this Structure==
==About this Structure==
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[[Category: Ig-super family domain]]
[[Category: Ig-super family domain]]
[[Category: Rossmann fold]]
[[Category: Rossmann fold]]
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