1l6z

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{{STRUCTURE_1l6z| PDB=1l6z | SCENE= }}
{{STRUCTURE_1l6z| PDB=1l6z | SCENE= }}
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'''CRYSTAL STRUCTURE OF MURINE CEACAM1A[1,4]: A CORONAVIRUS RECEPTOR AND CELL ADHESION MOLECULE IN THE CEA FAMILY'''
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===CRYSTAL STRUCTURE OF MURINE CEACAM1A[1,4]: A CORONAVIRUS RECEPTOR AND CELL ADHESION MOLECULE IN THE CEA FAMILY===
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==Overview==
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CEACAM1 is a member of the carcinoembryonic antigen (CEA) family. Isoforms of murine CEACAM1 serve as receptors for mouse hepatitis virus (MHV), a murine coronavirus. Here we report the crystal structure of soluble murine sCEACAM1a[1,4], which is composed of two Ig-like domains and has MHV neutralizing activity. Its N-terminal domain has a uniquely folded CC' loop that encompasses key virus-binding residues. This is the first atomic structure of any member of the CEA family, and provides a prototypic architecture for functional exploration of CEA family members. We discuss the structural basis of virus receptor activities of murine CEACAM1 proteins, binding of Neisseria to human CEACAM1, and other homophilic and heterophilic interactions of CEA family members.
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{{ABSTRACT_PUBMED_11980704}}
==About this Structure==
==About this Structure==
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[[Category: Coronavirus receptor]]
[[Category: Coronavirus receptor]]
[[Category: Ig-like domain]]
[[Category: Ig-like domain]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 23:36:41 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 2 11:50:34 2008''

Revision as of 08:50, 2 July 2008

Image:1l6z.png

Template:STRUCTURE 1l6z

CRYSTAL STRUCTURE OF MURINE CEACAM1A[1,4]: A CORONAVIRUS RECEPTOR AND CELL ADHESION MOLECULE IN THE CEA FAMILY

Template:ABSTRACT PUBMED 11980704

About this Structure

1L6Z is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.

Reference

Crystal structure of murine sCEACAM1a[1,4]: a coronavirus receptor in the CEA family., Tan K, Zelus BD, Meijers R, Liu JH, Bergelson JM, Duke N, Zhang R, Joachimiak A, Holmes KV, Wang JH, EMBO J. 2002 May 1;21(9):2076-86. PMID:11980704

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