Journal:Science:1
Structural basis of transcription activationYu Feng, Yu Zhang, Richard H. Ebright [1] Molecular Tour TAP, RNAP holoenzyme, DNA and RNA. To obtain a structure of TAP-RPo, we used a nucleic-acid scaffold corresponding to positions –57 to +15 (-54 to +11 shown) of a class II TAP-dependent promoter (positions numbered relative to transcription start site). Pink, nontemplate strand; red, template strand. The scaffold contained a consensus DNA site for TAP centered between positions –41 and –42 (TAP site: cyan, template strand; deeppink, nontemplate strand), a near-consensus extended –10 element (violet), a consensus –10 element (blue), a consensus discriminator element (royalblue), a consensus core recognition element, a 13-bp transcription bubble (maintained in the unwound state by having noncomplementary sequences on nontemplate and template strands), and UpCpGpA (in magenta). Comparison of TAP-DNA in TAP-RPo to CAP-DNA. TAP in cyan, CAP in skyblue. Click here to see animation of this scene. Protein-DNA interactions
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