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1nb7

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(New page: 200px<br /><applet load="1nb7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nb7, resolution 2.9&Aring;" /> '''HC-J4 RNA polymerase ...)
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[[Image:1nb7.gif|left|200px]]<br /><applet load="1nb7" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1nb7.gif|left|200px]]<br /><applet load="1nb7" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1nb7, resolution 2.9&Aring;" />
caption="1nb7, resolution 2.9&Aring;" />
'''HC-J4 RNA polymerase complexed with short RNA template strand'''<br />
'''HC-J4 RNA polymerase complexed with short RNA template strand'''<br />
==Overview==
==Overview==
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Several crystal structures of the hepatitis C virus NS5B protein, (genotype-1b, strain J4) complexed with metal ions, single-stranded RNA or, nucleoside-triphosphates have been determined. These complexes illustrate, how conserved amino acid side-chains, together with essential structural, features within the active site, control nucleotide binding and likely, mediate de-novo initiation. The incoming nucleotide interacts with several, basic residues from an extension on the NS5B fingers domain, a, beta-hairpin from the NS5B thumb domain and the C-terminal arm. The, modular, bi-partite fingers domain carries a long binding groove which, guides the template towards the catalytic site. The apo-polymerase, structure provides unprecedented insights into potential non-nucleoside, inhibitor binding sites located between palm and thumb near motif E, which, is unique to RNA polymerases and reverse transcriptases.
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Several crystal structures of the hepatitis C virus NS5B protein (genotype-1b, strain J4) complexed with metal ions, single-stranded RNA or nucleoside-triphosphates have been determined. These complexes illustrate how conserved amino acid side-chains, together with essential structural features within the active site, control nucleotide binding and likely mediate de-novo initiation. The incoming nucleotide interacts with several basic residues from an extension on the NS5B fingers domain, a beta-hairpin from the NS5B thumb domain and the C-terminal arm. The modular, bi-partite fingers domain carries a long binding groove which guides the template towards the catalytic site. The apo-polymerase structure provides unprecedented insights into potential non-nucleoside inhibitor binding sites located between palm and thumb near motif E, which is unique to RNA polymerases and reverse transcriptases.
==About this Structure==
==About this Structure==
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1NB7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Hepatitis_c_virus Hepatitis c virus] with MN as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/RNA-directed_RNA_polymerase RNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.48 2.7.7.48] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NB7 OCA].
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1NB7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Hepatitis_c_virus Hepatitis c virus] with <scene name='pdbligand=MN:'>MN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/RNA-directed_RNA_polymerase RNA-directed RNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.48 2.7.7.48] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NB7 OCA].
==Reference==
==Reference==
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[[Category: RNA-directed RNA polymerase]]
[[Category: RNA-directed RNA polymerase]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Farrell, D.J.O.]]
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[[Category: Farrell, D J.O.]]
[[Category: Jaeger, J.]]
[[Category: Jaeger, J.]]
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[[Category: Rowlands, D.J.]]
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[[Category: Rowlands, D J.]]
[[Category: Trowbridge, R.]]
[[Category: Trowbridge, R.]]
[[Category: MN]]
[[Category: MN]]
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[[Category: rna polymerase]]
[[Category: rna polymerase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:06:42 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:04:11 2008''

Revision as of 12:04, 21 February 2008


1nb7, resolution 2.9Å

Drag the structure with the mouse to rotate

HC-J4 RNA polymerase complexed with short RNA template strand

Overview

Several crystal structures of the hepatitis C virus NS5B protein (genotype-1b, strain J4) complexed with metal ions, single-stranded RNA or nucleoside-triphosphates have been determined. These complexes illustrate how conserved amino acid side-chains, together with essential structural features within the active site, control nucleotide binding and likely mediate de-novo initiation. The incoming nucleotide interacts with several basic residues from an extension on the NS5B fingers domain, a beta-hairpin from the NS5B thumb domain and the C-terminal arm. The modular, bi-partite fingers domain carries a long binding groove which guides the template towards the catalytic site. The apo-polymerase structure provides unprecedented insights into potential non-nucleoside inhibitor binding sites located between palm and thumb near motif E, which is unique to RNA polymerases and reverse transcriptases.

About this Structure

1NB7 is a Single protein structure of sequence from Hepatitis c virus with as ligand. Active as RNA-directed RNA polymerase, with EC number 2.7.7.48 Full crystallographic information is available from OCA.

Reference

Substrate complexes of hepatitis C virus RNA polymerase (HC-J4): structural evidence for nucleotide import and de-novo initiation., O'Farrell D, Trowbridge R, Rowlands D, Jager J, J Mol Biol. 2003 Feb 28;326(4):1025-35. PMID:12589751

Page seeded by OCA on Thu Feb 21 14:04:11 2008

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