4MTP
RdRp from Japanesese Encephalitis Virus
4MTP の概要
エントリーDOI | 10.2210/pdb4mtp/pdb |
関連するPDBエントリー | 4HDG 4HDH |
分子名称 | RNA dependent RNA polymerase, ZINC ION (2 entities in total) |
機能のキーワード | rna dependent rna polymerase, nucleotidyltransferases, apo, transferase |
由来する生物種 | Japanese encephalitis virus |
細胞内の位置 | Virion membrane; Multi-pass membrane protein: G3LHD9 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 292415.74 |
構造登録者 | |
主引用文献 | Surana, P.,Satchidanandam, V.,Nair, D.T. RNA-dependent RNA polymerase of Japanese encephalitis virus binds the initiator nucleotide GTP to form a mechanistically important pre-initiation state. Nucleic Acids Res., 42:2758-2773, 2014 Cited by PubMed Abstract: Flaviviral RNA-dependent RNA polymerases (RdRps) initiate replication of the single-stranded RNA genome in the absence of a primer. The template sequence 5'-CU-3' at the 3'-end of the flaviviral genome is highly conserved. Surprisingly, flaviviral RdRps require high concentrations of the second incoming nucleotide GTP to catalyze de novo template-dependent RNA synthesis. We show that GTP stimulates de novo RNA synthesis by RdRp from Japanese encephalitis virus (jRdRp) also. Crystal structures of jRdRp complexed with GTP and ATP provide a basis for specific recognition of GTP. Comparison of the jRdRpGTP structure with other viral RdRp-GTP structures shows that GTP binds jRdRp in a novel conformation. Apo-jRdRp structure suggests that the conserved motif F of jRdRp occupies multiple conformations in absence of GTP. Motif F becomes ordered on GTP binding and occludes the nucleotide triphosphate entry tunnel. Mutational analysis of key residues that interact with GTP evinces that the jRdRpGTP structure represents a novel pre-initiation state. Also, binding studies show that GTP binding reduces affinity of RdRp for RNA, but the presence of the catalytic Mn(2+) ion abolishes this inhibition. Collectively, these observations suggest that the observed pre-initiation state may serve as a checkpoint to prevent erroneous template-independent RNA synthesis by jRdRp during initiation. PubMed: 24293643DOI: 10.1093/nar/gkt1106 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.65 Å) |
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