2lll | pdb_00002lll
From Proteopedia
Solution NMR structure of C-terminal globular domain of human Lamin-B2, Northeast Structural Genomics Consortium target HR8546A
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Structural highlights
Disease[LMNB2_HUMAN] Partial acquired lipodystrophy. The disease is caused by mutations affecting the gene represented in this entry. Function[LMNB2_HUMAN] Lamins are components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane, which is thought to provide a framework for the nuclear envelope and may also interact with chromatin. Contents | ||||||||||||||||||
This page was last modified 10:13, 12 May 2021.