1qu0: Difference between revisions
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{{STRUCTURE_1qu0| PDB=1qu0 | SCENE= }} | {{STRUCTURE_1qu0| PDB=1qu0 | SCENE= }} | ||
===CRYSTAL STRUCTURE OF THE FIFTH LAMININ G-LIKE MODULE OF THE MOUSE LAMININ ALPHA2 CHAIN=== | |||
{{ABSTRACT_PUBMED_10619025}} | |||
== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/LAMA2_MOUSE LAMA2_MOUSE]] Note=Defects in Lama2 are a cause of murine muscular dystrophy (dy2J). | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/LAMA2_MOUSE LAMA2_MOUSE]] Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:010619025</ref><references group="xtra"/> | <ref group="xtra">PMID:010619025</ref><references group="xtra"/><references/> | ||
[[Category: Mus musculus]] | [[Category: Mus musculus]] | ||
[[Category: Hohenester, E.]] | [[Category: Hohenester, E.]] | ||
