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7MW8

Crystal Structure Analysis of Xac Nucleotide Pyrophosphatase/Phosphodiesterase

Summary for 7MW8
Entry DOI10.2210/pdb7mw8/pdb
DescriptorPhosphodiesterase-nucleotide pyrophosphatase, pApG, ZINC ION, ... (4 entities in total)
Functional Keywordshydrolase, enzyme, nucleotide, pyrophosphatase, phosphodiesterase, bacterial
Biological sourceXanthomonas citri
More
Total number of polymer chains12
Total formula weight280524.76
Authors
Fernandez, D.,Li, L.,Brown, J.A. (deposition date: 2021-05-15, release date: 2022-05-18, Last modification date: 2024-10-23)
Primary citationCarozza, J.A.,Cordova, A.F.,Brown, J.A.,AlSaif, Y.,Bohnert, V.,Cao, X.,Mardjuki, R.E.,Skariah, G.,Fernandez, D.,Li, L.
ENPP1's regulation of extracellular cGAMP is a ubiquitous mechanism of attenuating STING signaling.
Proc.Natl.Acad.Sci.USA, 119:e2119189119-e2119189119, 2022
Cited by
PubMed Abstract: The metazoan innate immune second messenger 2′3′-cGAMP is present both inside and outside cells. However, only extracellular cGAMP can be negatively regulated by the extracellular hydrolase ENPP1. Here, we determine whether ENPP1’s regulation of extracellular cGAMP is a ubiquitous mechanism of attenuating stimulator of interferon genes (STING) signaling. We identified ENPP1H362A, a point mutation that cannot degrade the 2′-5′ linkage in cGAMP while maintaining otherwise normal function. The selectivity of this histidine is conserved down to bacterial nucleotide pyrophosphatase/phosphodiesterase (NPP), allowing structural analysis and suggesting an unexplored ancient history of 2′-5′ cyclic dinucleotides. Enpp1H362A mice demonstrated that extracellular cGAMP is not responsible for the devastating phenotype in ENPP1-null humans and mice but is responsible for antiviral immunity and systemic inflammation. Our data define extracellular cGAMP as a pivotal STING activator, identify an evolutionarily critical role for ENPP1 in regulating inflammation, and suggest a therapeutic strategy for viral and inflammatory conditions by manipulating ENPP1 activity.
PubMed: 35588451
DOI: 10.1073/pnas.2119189119
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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