4nn0

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Template:STRUCTURE 4nn0

Contents

Crystal structure of the C1QTNF5 globular domain in space group P63

Template:ABSTRACT PUBMED 24531000

Disease

[C1QT5_HUMAN] Late-onset retinal degeneration. The disease is caused by mutations affecting the gene represented in this entry.

About this Structure

4nn0 is a 3 chain structure with sequence from Human. Full crystallographic information is available from OCA.

Reference

  • Tu X, Palczewski K. The macular degeneration-linked C1QTNF5 (S163) mutation causes higher-order structural rearrangements. J Struct Biol. 2014 Feb 12. pii: S1047-8477(14)00025-2. doi:, 10.1016/j.jsb.2014.02.001. PMID:24531000 doi:http://dx.doi.org/10.1016/j.jsb.2014.02.001

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