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4HRH

Crystal Structure of p11-Annexin A2(N-terminal) Fusion Protein in Complex with SMARCA3 Peptide

Summary for 4HRH
Entry DOI10.2210/pdb4hrh/pdb
DescriptorProtein S100-A10, Annexin A2, Helicase-like transcription factor, SULFATE ION (3 entities in total)
Functional Keywordsef-hand, calcium-binding protein
Biological sourceHomo sapiens (human)
More
Cellular locationSecreted, extracellular space, extracellular matrix, basement membrane : P07355
Cytoplasm : Q14527
Total number of polymer chains4
Total formula weight30687.07
Authors
Gao, P.,Patel, D.J. (deposition date: 2012-10-27, release date: 2013-03-06, Last modification date: 2023-09-20)
Primary citationOh, 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
Cited by
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
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.001 Å)
Structure validation

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