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7JIB

Room Temperature Crystal Structure of Nsp10/Nsp16 from SARS-CoV-2 with Substrates and Products of 2'-O-methylation of the Cap-1

Summary for 7JIB
Entry DOI10.2210/pdb7jib/pdb
Related6W4H 6WJT 6WKQ 6WQ3 6WRZ 6WVN 6XKM 7JHE
Descriptor2'-O-methyltransferase, Non-structural protein 10, CHLORIDE ION, ... (10 entities in total)
Functional Keywordssars cov-2, methyltransferase, m7gpppa, cap-0, cap-1, sah, sam, structural genomics, center for structural genomics of infectious diseases, csgid, viral protein
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV)
More
Total number of polymer chains2
Total formula weight51814.39
Authors
Primary citationWilamowski, M.,Sherrell, D.A.,Minasov, G.,Kim, Y.,Shuvalova, L.,Lavens, A.,Chard, R.,Maltseva, N.,Jedrzejczak, R.,Rosas-Lemus, M.,Saint, N.,Foster, I.T.,Michalska, K.,Satchell, K.J.F.,Joachimiak, A.
2'-O methylation of RNA cap in SARS-CoV-2 captured by serial crystallography.
Proc.Natl.Acad.Sci.USA, 118:-, 2021
Cited by
PubMed Abstract: The genome of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) coronavirus has a capping modification at the 5'-untranslated region (UTR) to prevent its degradation by host nucleases. These modifications are performed by the Nsp10/14 and Nsp10/16 heterodimers using S-adenosylmethionine as the methyl donor. Nsp10/16 heterodimer is responsible for the methylation at the ribose 2'-O position of the first nucleotide. To investigate the conformational changes of the complex during 2'-O methyltransferase activity, we used a fixed-target serial synchrotron crystallography method at room temperature. We determined crystal structures of Nsp10/16 with substrates and products that revealed the states before and after methylation, occurring within the crystals during the experiments. Here we report the crystal structure of Nsp10/16 in complex with Cap-1 analog (GpppA). Inhibition of Nsp16 activity may reduce viral proliferation, making this protein an attractive drug target.
PubMed: 33972410
DOI: 10.1073/pnas.2100170118
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.65 Å)
Structure validation

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数据于2024-11-06公开中

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