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4lg6

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'''Unreleased structure'''
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{{STRUCTURE_4lg6| PDB=4lg6 | SCENE= }}
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===Crystal structure of ANKRA2-CCDC8 complex===
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The entry 4lg6 is ON HOLD
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==Disease==
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[[http://www.uniprot.org/uniprot/CCDC8_HUMAN CCDC8_HUMAN]] 3M syndrome. The disease is caused by mutations affecting the gene represented in this entry.
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Authors: Xu, C., Bian, C., Tempel, W., Mackenzie, F., Bountra, C., Arrowsmith, C.H., Edwards, A.M., Min, J., Structural Genomics Consortium (SGC)
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==Function==
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[[http://www.uniprot.org/uniprot/ANRA2_HUMAN ANRA2_HUMAN]] May facilitate endocytosis by linking megalin to components of the cytoskeleton or endocytic machinery.
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Description: Crystal structure of ANKRA2-CCDC8 complex
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==About this Structure==
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[[4lg6]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LG6 OCA].
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[[Category: Homo sapiens]]
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[[Category: Arrowsmith, C H.]]
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[[Category: Bian, C.]]
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[[Category: Bountra, C.]]
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[[Category: Edwards, A M.]]
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[[Category: Mackenzie, F.]]
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[[Category: Min, J.]]
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[[Category: SGC, Structural Genomics Consortium.]]
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[[Category: Tempel, W.]]
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[[Category: Xu, C.]]
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[[Category: Ankyrin repeat]]
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[[Category: Sgc]]
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[[Category: Structural genomics consortium]]
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[[Category: Structural protein]]

Revision as of 08:20, 29 September 2013

Template:STRUCTURE 4lg6

Contents

Crystal structure of ANKRA2-CCDC8 complex

Disease

[CCDC8_HUMAN] 3M syndrome. The disease is caused by mutations affecting the gene represented in this entry.

Function

[ANRA2_HUMAN] May facilitate endocytosis by linking megalin to components of the cytoskeleton or endocytic machinery.

About this Structure

4lg6 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

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OCA

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