2yz1

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(New page: 200px<br /><applet load="2yz1" size="350" color="white" frame="true" align="right" spinBox="true" caption="2yz1, resolution 1.40&Aring;" /> '''Crystal structure of...)
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==Overview==
==Overview==
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SRC homology 2 domain-containing protein tyrosine phosphatase substrate 1, (SHPS-1 or SIRPalpha/BIT) is an immunoglobulin (Ig) superfamily, transmembrane receptor and a member of the signal regulatory protein, (SIRP) family involved in cell-cell interaction. SHPS-1 binds to its, ligand CD47 to relay an inhibitory signal for cellular responses, whereas, SIRPbeta, an activating member of the same family, does not bind to CD47, despite sharing a highly homologous ligand-binding domain with SHPS-1. To, address the molecular basis for specific CD47 recognition by SHPS-1, we, present the crystal structure of the ligand-binding domain of murine, SHPS-1 (mSHPS-1). Folding topology revealed that mSHPS-1 adopts an I2-set, Ig fold, but its overall structure resembles IgV domains of antigen, receptors, although it has an extended loop structure (C'E loop), which, forms a dimer interface in the crystal. Site-directed mutagenesis studies, of mSHPS-1 identified critical residues for CD47 binding including sites, in the C'E loop and regions corresponding to complementarity-determining, regions of antigen receptors. The structural and functional features of, mSHPS-1 are consistent with the human SHPS-1 structure except that human, SHPS-1 has an additional beta-strand D. These results suggest that the, variable complementarity-determining region-like loop structures in the, binding surface of SHPS-1 are generally required for ligand recognition in, a manner similar to that of antigen receptors, which may explain the, diverse ligand-binding specificities of SIRP family receptors.
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SRC homology 2 domain-containing protein tyrosine phosphatase substrate 1 (SHPS-1 or SIRP alpha/BIT) is an immunoglobulin (Ig) superfamily transmembrane receptor and a member of the signal regulatory protein (SIRP) family involved in cell-cell interaction. SHPS-1 binds to its ligand CD47 to relay an inhibitory signal for cellular responses, whereas SIRPbeta, an activating member of the same family, does not bind to CD47 despite sharing a highly homologous ligand-binding domain with SHPS-1. To address the molecular basis for specific CD47 recognition by SHPS-1, we present the crystal structure of the ligand-binding domain of murine SHPS-1 (mSHPS-1). Folding topology revealed that mSHPS-1 adopts an I2-set Ig fold, but its overall structure resembles IgV domains of antigen receptors, although it has an extended loop structure (C'E loop), which forms a dimer interface in the crystal. Site-directed mutagenesis studies of mSHPS-1 identified critical residues for CD47 binding including sites in the C'E loop and regions corresponding to complementarity-determining regions of antigen receptors. The structural and functional features of mSHPS-1 are consistent with the human SHPS-1 structure except that human SHPS-1 has an additional beta-strand D. These results suggest that the variable complementarity-determining region-like loop structures in the binding surface of SHPS-1 are generally required for ligand recognition in a manner similar to that of antigen receptors, which may explain the diverse ligand-binding specificities of SIRP family receptors.
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
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Structural Insight into the Specific Interaction between Murine SHPS-1/SIRPalpha and Its Ligand CD47., Nakaishi A, Hirose M, Yoshimura M, Oneyama C, Saito K, Kuki N, Matsuda M, Honma N, Ohnishi H, Matozaki T, Okada M, Nakagawa A, J Mol Biol. 2007 Nov 7;. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=18045614 18045614]
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Structural insight into the specific interaction between murine SHPS-1/SIRP alpha and its ligand CD47., Nakaishi A, Hirose M, Yoshimura M, Oneyama C, Saito K, Kuki N, Matsuda M, Honma N, Ohnishi H, Matozaki T, Okada M, Nakagawa A, J Mol Biol. 2008 Jan 18;375(3):650-60. Epub 2007 Nov 7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=18045614 18045614]
[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: transmembrane]]
[[Category: transmembrane]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 11:14:08 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:58:51 2008''

Revision as of 16:58, 21 February 2008


2yz1, resolution 1.40Å

Drag the structure with the mouse to rotate

Crystal structure of the ligand-binding domain of murine SHPS-1/SIRP alpha

Overview

SRC homology 2 domain-containing protein tyrosine phosphatase substrate 1 (SHPS-1 or SIRP alpha/BIT) is an immunoglobulin (Ig) superfamily transmembrane receptor and a member of the signal regulatory protein (SIRP) family involved in cell-cell interaction. SHPS-1 binds to its ligand CD47 to relay an inhibitory signal for cellular responses, whereas SIRPbeta, an activating member of the same family, does not bind to CD47 despite sharing a highly homologous ligand-binding domain with SHPS-1. To address the molecular basis for specific CD47 recognition by SHPS-1, we present the crystal structure of the ligand-binding domain of murine SHPS-1 (mSHPS-1). Folding topology revealed that mSHPS-1 adopts an I2-set Ig fold, but its overall structure resembles IgV domains of antigen receptors, although it has an extended loop structure (C'E loop), which forms a dimer interface in the crystal. Site-directed mutagenesis studies of mSHPS-1 identified critical residues for CD47 binding including sites in the C'E loop and regions corresponding to complementarity-determining regions of antigen receptors. The structural and functional features of mSHPS-1 are consistent with the human SHPS-1 structure except that human SHPS-1 has an additional beta-strand D. These results suggest that the variable complementarity-determining region-like loop structures in the binding surface of SHPS-1 are generally required for ligand recognition in a manner similar to that of antigen receptors, which may explain the diverse ligand-binding specificities of SIRP family receptors.

About this Structure

2YZ1 is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.

Reference

Structural insight into the specific interaction between murine SHPS-1/SIRP alpha and its ligand CD47., Nakaishi A, Hirose M, Yoshimura M, Oneyama C, Saito K, Kuki N, Matsuda M, Honma N, Ohnishi H, Matozaki T, Okada M, Nakagawa A, J Mol Biol. 2008 Jan 18;375(3):650-60. Epub 2007 Nov 7. PMID:18045614

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