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
DiseaseLMNB2_HUMAN Partial acquired lipodystrophy. The disease is caused by mutations affecting the gene represented in this entry. FunctionLMNB2_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 11:06, 15 February 2023.