2pi4

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==Overview==
==Overview==
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DNA-directed RNA polymerases are capable of initiating synthesis of RNA, without primers, the first catalytic stage of initiation is referred to as, de novo RNA synthesis. De novo synthesis is a unique phase in the, transcription cycle where the RNA polymerase binds two nucleotides rather, than a nascent RNA polymer and a single nucleotide. For bacteriophage T7, RNA polymerase, transcription begins with a marked preference for GTP at, the +1 and +2 positions. We determined the crystal structures of T7 RNA, polymerase complexes captured during the de novo RNA synthesis. The DNA, substrates in the structures in the complexes contain a common Phi10, duplex promoter followed by a unique five base single-stranded extension, of template DNA whose sequences varied at positions +1 and +2, thereby, allowing for different pairs of initiating nucleotides GTP, ATP, CTP or, UTP to bind. The structures show that the initiating nucleotides bind RNA, polymerase in locations distinct from those described previously for, elongation complexes. Selection bias in favor of GTP as an initiating, nucleotide is accomplished by shape complementarity, extensive protein, side-chain and strong base-stacking interactions for the guanine moiety in, the enzyme active site. Consequently, an initiating GTP provides the, largest stabilization force for the open promoter conformation.
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DNA-directed RNA polymerases are capable of initiating synthesis of RNA without primers, the first catalytic stage of initiation is referred to as de novo RNA synthesis. De novo synthesis is a unique phase in the transcription cycle where the RNA polymerase binds two nucleotides rather than a nascent RNA polymer and a single nucleotide. For bacteriophage T7 RNA polymerase, transcription begins with a marked preference for GTP at the +1 and +2 positions. We determined the crystal structures of T7 RNA polymerase complexes captured during the de novo RNA synthesis. The DNA substrates in the structures in the complexes contain a common Phi 10 duplex promoter followed by a unique five base single-stranded extension of template DNA whose sequences varied at positions +1 and +2, thereby allowing for different pairs of initiating nucleotides GTP, ATP, CTP or UTP to bind. The structures show that the initiating nucleotides bind RNA polymerase in locations distinct from those described previously for elongation complexes. Selection bias in favor of GTP as an initiating nucleotide is accomplished by shape complementarity, extensive protein side-chain and strong base-stacking interactions for the guanine moiety in the enzyme active site. Consequently, an initiating GTP provides the largest stabilization force for the open promoter conformation.
==About this Structure==
==About this Structure==
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[[Category: DNA-directed RNA polymerase]]
[[Category: DNA-directed RNA polymerase]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Kennedy, W.P.]]
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[[Category: Kennedy, W P.]]
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[[Category: Momand, J.R.]]
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[[Category: Momand, J R.]]
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[[Category: Yin, Y.W.]]
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[[Category: Yin, Y W.]]
[[Category: GH3]]
[[Category: GH3]]
[[Category: MG]]
[[Category: MG]]
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[[Category: t7 rna polymerase]]
[[Category: t7 rna polymerase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:50:22 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:29:38 2008''

Revision as of 16:29, 21 February 2008


2pi4, resolution 2.50Å

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T7RNAP complexed with a phi10 protein and initiating GTPs.

Overview

DNA-directed RNA polymerases are capable of initiating synthesis of RNA without primers, the first catalytic stage of initiation is referred to as de novo RNA synthesis. De novo synthesis is a unique phase in the transcription cycle where the RNA polymerase binds two nucleotides rather than a nascent RNA polymer and a single nucleotide. For bacteriophage T7 RNA polymerase, transcription begins with a marked preference for GTP at the +1 and +2 positions. We determined the crystal structures of T7 RNA polymerase complexes captured during the de novo RNA synthesis. The DNA substrates in the structures in the complexes contain a common Phi 10 duplex promoter followed by a unique five base single-stranded extension of template DNA whose sequences varied at positions +1 and +2, thereby allowing for different pairs of initiating nucleotides GTP, ATP, CTP or UTP to bind. The structures show that the initiating nucleotides bind RNA polymerase in locations distinct from those described previously for elongation complexes. Selection bias in favor of GTP as an initiating nucleotide is accomplished by shape complementarity, extensive protein side-chain and strong base-stacking interactions for the guanine moiety in the enzyme active site. Consequently, an initiating GTP provides the largest stabilization force for the open promoter conformation.

About this Structure

2PI4 is a Single protein structure of sequence from Bacteriophage t7 with and as ligands. Active as DNA-directed RNA polymerase, with EC number 2.7.7.6 Full crystallographic information is available from OCA.

Reference

Mechanism for de novo RNA synthesis and initiating nucleotide specificity by t7 RNA polymerase., Kennedy WP, Momand JR, Yin YW, J Mol Biol. 2007 Jul 6;370(2):256-68. Epub 2007 Mar 21. PMID:17512007

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