2c35: Difference between revisions

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New page: left|200px<br /> <applet load="2c35" size="450" color="white" frame="true" align="right" spinBox="true" caption="2c35, resolution 2.7Å" /> '''SUBUNITS RPB4 AND RP...
 
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[[Image:2c35.gif|left|200px]]<br />
[[Image:2c35.gif|left|200px]]<br /><applet load="2c35" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2c35" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2c35, resolution 2.7&Aring;" />
caption="2c35, resolution 2.7&Aring;" />
'''SUBUNITS RPB4 AND RPB7 OF HUMAN RNA POLYMERASE II'''<br />
'''SUBUNITS RPB4 AND RPB7 OF HUMAN RNA POLYMERASE II'''<br />


==Overview==
==Overview==
The Rpb4 and Rpb7 subunits of eukaryotic RNA polymerase II (RNAP(II)) form, a heterodimer that protrudes from the 10-subunit core of the enzyme. We, have obtained crystals of the human Rpb4/Rpb7 heterodimer and determined, the structure to 2.7 A resolution. The presence of putative RNA-binding, domains on the Rpb7 subunit and the position of the heterodimer close to, the RNA exit groove in the 12 subunit yeast polymerase complex strongly, suggests a role for the heterodimer in binding and stabilizing the nascent, RNA transcript. We have complemented the structural analysis with, biochemical studies directed at dissecting the RNA-binding properties of, the human Rpb4/Rpb7 complex and that of the homologous E/F complex from, Methanocaldococcus jannaschii. A number of conserved, solvent-exposed, residues in both the human Rpb7 subunit and the archaeal E subunit have, been modified by site-directed mutagenesis and the mutants tested for RNA, binding by performing electrophoretic mobility shift assays. These studies, have identified an elongated surface region on the corresponding face of, both subunit E and Rpb7 that is involved in RNA binding. The area spans, the nucleic acid binding face of the OB fold, including the B4-B5 loop, but also extends towards the N-terminal domain.
The Rpb4 and Rpb7 subunits of eukaryotic RNA polymerase II (RNAP(II)) form a heterodimer that protrudes from the 10-subunit core of the enzyme. We have obtained crystals of the human Rpb4/Rpb7 heterodimer and determined the structure to 2.7 A resolution. The presence of putative RNA-binding domains on the Rpb7 subunit and the position of the heterodimer close to the RNA exit groove in the 12 subunit yeast polymerase complex strongly suggests a role for the heterodimer in binding and stabilizing the nascent RNA transcript. We have complemented the structural analysis with biochemical studies directed at dissecting the RNA-binding properties of the human Rpb4/Rpb7 complex and that of the homologous E/F complex from Methanocaldococcus jannaschii. A number of conserved, solvent-exposed residues in both the human Rpb7 subunit and the archaeal E subunit have been modified by site-directed mutagenesis and the mutants tested for RNA binding by performing electrophoretic mobility shift assays. These studies have identified an elongated surface region on the corresponding face of both subunit E and Rpb7 that is involved in RNA binding. The area spans the nucleic acid binding face of the OB fold, including the B4-B5 loop, but also extends towards the N-terminal domain.


==About this Structure==
==About this Structure==
2C35 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/DNA-directed_RNA_polymerase DNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.6 2.7.7.6] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2C35 OCA].  
2C35 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/DNA-directed_RNA_polymerase DNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.6 2.7.7.6] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2C35 OCA].  


==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Brick, P.]]
[[Category: Brick, P.]]
[[Category: Cordell, S.C.]]
[[Category: Cordell, S C.]]
[[Category: Meka, H.]]
[[Category: Meka, H.]]
[[Category: Onesti, S.]]
[[Category: Onesti, S.]]
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[[Category: transcription]]
[[Category: transcription]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 21:10:12 2007''
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