4HRG

Crystal Structure of p11-Annexin A2(N-terminal) Fusion Protein in Complex with AHNAK1 Peptide

4HRG の概要

• エントリーDOI: 10.2210/pdb4hrg/pdb
• 分子名称: Protein S100-A10, Neuroblast differentiation-associated protein AHNAK (3 entities in total)
• 機能のキーワード: ef-hand, calcium-binding protein
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Nucleus: Q09666
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 30227.14

構造登録者

Gao, P.,Patel, D.J. (登録日: 2012-10-27, 公開日: 2013-03-06, 最終更新日: 2023-09-20)

主引用文献

Oh, Y.S.,Gao, P.,Lee, K.W.,Ceglia, I.,Seo, J.S.,Zhang, X.,Ahn, J.H.,Chait, B.T.,Patel, D.J.,Kim, Y.,Greengard, P.
SMARCA3, a Chromatin-Remodeling Factor, Is Required for p11-Dependent Antidepressant Action.
Cell(Cambridge,Mass.), 152:831-843, 2013

PubMed Abstract: p11, through unknown mechanisms, is required for behavioral and cellular responses to selective serotonin reuptake inhibitors (SSRIs). We show that SMARCA3, a chromatin-remodeling factor, is a target for the p11/annexin A2 heterotetrameric complex. Determination of the crystal structure indicates that SMARCA3 peptide binds to a hydrophobic pocket in the heterotetramer. Formation of this complex increases the DNA-binding affinity of SMARCA3 and its localization to the nuclear matrix fraction. In the dentate gyrus, both p11 and SMARCA3 are highly enriched in hilar mossy cells and basket cells. The SSRI fluoxetine induces expression of p11 in both cell types and increases the amount of the ternary complex of p11/annexin A2/SMARCA3. SSRI-induced neurogenesis and behavioral responses are abolished by constitutive knockout of SMARCA3. Our studies indicate a central role for a chromatin-remodeling factor in the SSRI/p11 signaling pathway and suggest an approach to the development of improved antidepressant therapies. PAPERCLIP:

PubMed: 23415230
DOI: 10.1016/j.cell.2013.01.014

実験手法

X-RAY DIFFRACTION (2.0001 Å)