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8EAE

Structure of Ternary Complex of cGAS with dsDNA and Bound 5-pppG(2,5)pI

Summary for 8EAE
Entry DOI10.2210/pdb8eae/pdb
DescriptorCyclic GMP-AMP synthase, Palindromic DNA18, [[(2~{R},3~{R},4~{R},5~{R})-5-(2-azanyl-6-oxidanylidene-1~{H}-purin-9-yl)-4-[[(2~{R},3~{S},4~{R},5~{R})-3,4-bis(oxidanyl)-5-(6-oxidanylidene-1~{H}-purin-9-yl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl]oxy-3-oxidanyl-oxolan-2-yl]methoxy-oxidanyl-phosphoryl] phosphono hydrogen phosphate, ... (6 entities in total)
Functional Keywordstransferase-dna complex, cgas, pppg(2, 5)pi, immune system, transferase/dna
Biological sourceMus musculus (house mouse)
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Total number of polymer chains6
Total formula weight109225.09
Authors
Wu, S.,Sohn, J. (deposition date: 2022-08-29, release date: 2023-10-25, Last modification date: 2024-05-29)
Primary citationWu, S.,Gabelli, S.B.,Sohn, J.
The structural basis for 2'-5'/3'-5'-cGAMP synthesis by cGAS.
Nat Commun, 15:4012-4012, 2024
Cited by
PubMed Abstract: cGAS activates innate immune responses against cytosolic double-stranded DNA. Here, by determining crystal structures of cGAS at various reaction stages, we report a unifying catalytic mechanism. apo-cGAS assumes an array of inactive conformations and binds NTPs nonproductively. Dimerization-coupled double-stranded DNA-binding then affixes the active site into a rigid lock for productive metal•substrate binding. A web-like network of protein•NTP, intra-NTP, and inter-NTP interactions ensures the stepwise synthesis of 2'-5'/3'-5'-linked cGAMP while discriminating against noncognate NTPs and off-pathway intermediates. One divalent metal is sufficient for productive substrate binding, and capturing the second divalent metal is tightly coupled to nucleotide and linkage specificities, a process which manganese is preferred over magnesium by 100-fold. Additionally, we elucidate how mouse cGAS achieves more stringent NTP and linkage specificities than human cGAS. Together, our results reveal that an adaptable, yet precise lock-and-key-like mechanism underpins cGAS catalysis.
PubMed: 38740774
DOI: 10.1038/s41467-024-48365-3
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.56 Å)
Structure validation

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