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8TDV

ssRNA bound SAMHD1 T closed

Summary for 8TDV
Entry DOI10.2210/pdb8tdv/pdb
EMDB information41174
DescriptorDeoxynucleoside triphosphate triphosphohydrolase SAMHD1, RNA (5'-R(P*CP*CP*GP*GP*CP*C)-3'), RNA (5'-R(P*CP*CP*GP*AP*CP*CP*C)-3'), ... (4 entities in total)
Functional Keywordsdeoxynucleoside triphosphate triphosphohydrolase, hydrolase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight293354.89
Authors
Sung, M.,Huynh, K.,Han, S. (deposition date: 2023-07-05, release date: 2023-12-20)
Primary citationOrris, B.,Sung, M.W.,Bhat, S.,Xu, Y.,Huynh, K.W.,Han, S.,Johnson, D.C.,Bosbach, B.,Shields, D.J.,Stivers, J.T.
Guanine-containing ssDNA and RNA induce dimeric and tetrameric structural forms of SAMHD1.
Nucleic Acids Res., 51:12443-12458, 2023
Cited by
PubMed Abstract: The dNTPase activity of tetrameric SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 (SAMHD1) plays a critical role in cellular dNTP regulation. SAMHD1 also associates with stalled DNA replication forks, DNA repair foci, ssRNA and telomeres. The above functions require nucleic acid binding by SAMHD1, which may be modulated by its oligomeric state. Here we establish in cryo-EM and biochemical studies that the guanine-specific A1 activator site of each SAMHD1 monomer is used to target the enzyme to guanine nucleotides within single-stranded (ss) DNA and RNA. Remarkably, nucleic acid strands containing a single guanine base induce dimeric SAMHD1, while two or more guanines with ∼20 nucleotide spacing induce a tetrameric form. A cryo-EM structure of ssRNA-bound tetrameric SAMHD1 shows how ssRNA strands bridge two SAMHD1 dimers and stabilize the structure. This ssRNA-bound tetramer is inactive with respect to dNTPase and RNase activity.
PubMed: 37930833
DOI: 10.1093/nar/gkad971
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.44 Å)
Structure validation

226707

数据于2024-10-30公开中

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