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Deazaguanylation is a nucleobase-protein conjugation required for type IV CBASS immunity

delete2025-09-25
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OA
AI
D
Douglas R. Wassarman
P
Patrick Pfaff
J
João A. Paulo
S
Steven P. Gygi
K
Kevan M. Shokat
P
Philip J. Kranzusch *
DOI:10.1126/science.adx6053delete
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Abstract

Abstract

En 中文
Bacteria, plant, and animal cells modify nucleic acids by incorporating chemical analogs of standard nucleobases. Queuine and other 7-deazapurine nucleobase analogs are commonly incorporated into tRNA and are nucleic acid modifications required for the regulation of cellular gene expression. Wassarman et al. discovered that bacterial antiphage defense enzymes can also attach 7-deazapurines to proteins, generating an N-terminal 7-amido-7-deazaguanine (NDG) modification through a conjugation reaction. Structures of the enzymes involved in this process reveal homology to canonical queuine biosynthetic enzymes and explain how NDG is attached to proteins to control immune activation. —Di Jiang

Journal

Science cover
Science
IF:
45.8
Papers:
1.4W
Citations:
78.6W

Organization

U
university of california
Scholars:
1.9W
Papers: 8.0K
Citations: 10
H
Harvard Medical School
Scholars:
6.5W
Papers: 4.8W
Citations: 91