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4K8V

Structure of cyclic GMP-AMP Synthase (cGAS)

Summary for 4K8V
Entry DOI10.2210/pdb4k8v/pdb
Related4K96 4K97 4K98 4K99 4K9A 4K9B
DescriptorCyclic GMP-AMP synthase, ZINC ION (3 entities in total)
Functional Keywordsnucleotidyltransferase, dna, transferase
Biological sourceMus musculus (mouse)
Cellular locationCytoplasm, cytosol: Q8C6L5
Total number of polymer chains4
Total formula weight170310.12
Authors
Gao, P.,Wu, Y.,Patel, D.J. (deposition date: 2013-04-18, release date: 2013-05-15, Last modification date: 2024-02-28)
Primary citationGao, P.,Ascano, M.,Wu, Y.,Barchet, W.,Gaffney, B.L.,Zillinger, T.,Serganov, A.A.,Liu, Y.,Jones, R.A.,Hartmann, G.,Tuschl, T.,Patel, D.J.
Cyclic [G(2',5')pA(3',5')p] is the metazoan second messenger produced by DNA-activated cyclic GMP-AMP synthase.
Cell(Cambridge,Mass.), 153:1094-1107, 2013
Cited by
PubMed Abstract: Recent studies identified cyclic GMP-AMP (cGAMP) as a metazoan second messenger triggering an interferon response. cGAMP is generated from GTP and ATP by cytoplasmic dsDNA sensor cGAMP synthase (cGAS). We combined structural, chemical, biochemical, and cellular assays to demonstrate that this second messenger contains G(2',5')pA and A(3',5')pG phosphodiester linkages, designated c[G(2',5')pA(3',5')p]. We show that, upon dsDNA binding, cGAS is activated through conformational transitions, resulting in formation of a catalytically competent and accessible nucleotide-binding pocket for generation of c[G(2',5')pA(3',5')p]. We demonstrate that cyclization occurs in a stepwise manner through initial generation of 5'-pppG(2',5')pA prior to cyclization to c[G(2',5')pA(3',5')p], with the latter positioned precisely in the catalytic pocket. Mutants of cGAS dsDNA-binding or catalytic pocket residues exhibit reduced or abrogated activity. Our studies have identified c[G(2',5')pA(3',5')p] as a founding member of a family of metazoan 2',5'-containing cyclic heterodinucleotide second messengers distinct from bacterial 3',5' cyclic dinucleotides.
PubMed: 23647843
DOI: 10.1016/j.cell.2013.04.046
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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数据于2024-11-06公开中

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