Neurexin: Difference between revisions
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== Relevance == | == Relevance == | ||
NRXN sequence variants may contribute to autism spectrum disorder and other cognitive diseases<ref>PMID:18179900</ref>. | NRXN sequence variants may contribute to autism spectrum disorder and other cognitive diseases<ref>PMID:18179900</ref>. | ||
== Structural highlights == | |||
The surface interaction between NRXN and neuroligin is mediated by a Ca+2 ion<ref>PMID:20543817</ref>. | |||
</StructureSection> | |||
== 3D Structures of Neurexin == | == 3D Structures of Neurexin == | ||
Revision as of 11:03, 8 May 2016
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3D Structures of Neurexin
08-May-2016
References
Proteopedia Page Contributors and Editors (what is this?)
Alexander Berchansky, Michal Harel, David Canner, Jaime Prilusky, Joel L. Sussman