2fvq

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(New page: 200px<br /><applet load="2fvq" size="450" color="white" frame="true" align="right" spinBox="true" caption="2fvq, resolution 2.3&Aring;" /> '''A Structural Study of...)
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caption="2fvq, resolution 2.3&Aring;" />
'''A Structural Study of the CA Dinucleotide Step in the Integrase Processing Site of Moloney Murine Leukemia Virus'''<br />
'''A Structural Study of the CA Dinucleotide Step in the Integrase Processing Site of Moloney Murine Leukemia Virus'''<br />
==Overview==
==Overview==
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In the first step of retroviral integration, integrase cleaves the linear, viral DNA within its long terminal repeat (LTR) immediately 3' to the CA, dinucleotide step, resulting in a reactive 3' OH on one strand and a 5', two base overhang on the complementary strand. In order to investigate the, structural properties of the 3' end processing site within the Moloney, murine leukemia virus (MMLV) LTR d(TCTTTCATT), a host-guest, crystallographic method was employed to determine the structures of four, self-complementary 16 bp oligonucleotides including LTR sequences, (underlined), d(TTTCATTGCAATGAAA), d(CTTTCATTAATGAAAG), d(TCTTTCATATGAAAGA) and d(CACAATGATCATTGTG), the guests, complexed with, the N-terminal fragment of MMLV reverse transcriptase, the host. The, structures of the LTR-containing oligonucleotides were compared to those, of non-LTR oligonucleotides crystallized in the same lattice. Properties, unique to the CA dinucleotide step within the LTR sequence, independent of, its position from the end of the duplex, include a positive roll angle and, negative slide value. This propensity for the CA dinucleotide step within, the MMLV LTR sequence to adopt only positive roll angles is likely, influenced by the more rigid, invariable 3' and 5' flanking TT, dinucleotide steps and may be important for specific recognition and/or, cleavage by the MMLV integrase.
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In the first step of retroviral integration, integrase cleaves the linear viral DNA within its long terminal repeat (LTR) immediately 3' to the CA dinucleotide step, resulting in a reactive 3' OH on one strand and a 5' two base overhang on the complementary strand. In order to investigate the structural properties of the 3' end processing site within the Moloney murine leukemia virus (MMLV) LTR d(TCTTTCATT), a host-guest crystallographic method was employed to determine the structures of four self-complementary 16 bp oligonucleotides including LTR sequences (underlined), d(TTTCATTGCAATGAAA), d(CTTTCATTAATGAAAG), d(TCTTTCATATGAAAGA) and d(CACAATGATCATTGTG), the guests, complexed with the N-terminal fragment of MMLV reverse transcriptase, the host. The structures of the LTR-containing oligonucleotides were compared to those of non-LTR oligonucleotides crystallized in the same lattice. Properties unique to the CA dinucleotide step within the LTR sequence, independent of its position from the end of the duplex, include a positive roll angle and negative slide value. This propensity for the CA dinucleotide step within the MMLV LTR sequence to adopt only positive roll angles is likely influenced by the more rigid, invariable 3' and 5' flanking TT dinucleotide steps and may be important for specific recognition and/or cleavage by the MMLV integrase.
==About this Structure==
==About this Structure==
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2FVQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Moloney_murine_leukemia_virus Moloney murine leukemia virus]. Active as [http://en.wikipedia.org/wiki/RNA-directed_DNA_polymerase RNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.49 2.7.7.49] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2FVQ OCA].
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2FVQ is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Moloney_murine_leukemia_virus Moloney murine leukemia virus]. Active as [http://en.wikipedia.org/wiki/RNA-directed_DNA_polymerase RNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.49 2.7.7.49] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FVQ OCA].
==Reference==
==Reference==
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[[Category: RNA-directed DNA polymerase]]
[[Category: RNA-directed DNA polymerase]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Cote, M.L.]]
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[[Category: Cote, M L.]]
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[[Category: Georgiadis, M.M.]]
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[[Category: Georgiadis, M M.]]
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[[Category: Montano, S.P.]]
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[[Category: Montano, S P.]]
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[[Category: Roth, M.J.]]
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[[Category: Roth, M J.]]
[[Category: ltr]]
[[Category: ltr]]
[[Category: mmlv]]
[[Category: mmlv]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 10:47:52 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:25:34 2008''

Revision as of 15:25, 21 February 2008


2fvq, resolution 2.3Å

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A Structural Study of the CA Dinucleotide Step in the Integrase Processing Site of Moloney Murine Leukemia Virus

Overview

In the first step of retroviral integration, integrase cleaves the linear viral DNA within its long terminal repeat (LTR) immediately 3' to the CA dinucleotide step, resulting in a reactive 3' OH on one strand and a 5' two base overhang on the complementary strand. In order to investigate the structural properties of the 3' end processing site within the Moloney murine leukemia virus (MMLV) LTR d(TCTTTCATT), a host-guest crystallographic method was employed to determine the structures of four self-complementary 16 bp oligonucleotides including LTR sequences (underlined), d(TTTCATTGCAATGAAA), d(CTTTCATTAATGAAAG), d(TCTTTCATATGAAAGA) and d(CACAATGATCATTGTG), the guests, complexed with the N-terminal fragment of MMLV reverse transcriptase, the host. The structures of the LTR-containing oligonucleotides were compared to those of non-LTR oligonucleotides crystallized in the same lattice. Properties unique to the CA dinucleotide step within the LTR sequence, independent of its position from the end of the duplex, include a positive roll angle and negative slide value. This propensity for the CA dinucleotide step within the MMLV LTR sequence to adopt only positive roll angles is likely influenced by the more rigid, invariable 3' and 5' flanking TT dinucleotide steps and may be important for specific recognition and/or cleavage by the MMLV integrase.

About this Structure

2FVQ is a Single protein structure of sequence from Moloney murine leukemia virus. Active as RNA-directed DNA polymerase, with EC number 2.7.7.49 Full crystallographic information is available from OCA.

Reference

Crystal structures of oligonucleotides including the integrase processing site of the Moloney murine leukemia virus., Montano SP, Cote ML, Roth MJ, Georgiadis MM, Nucleic Acids Res. 2006;34(19):5353-60. Epub 2006 Sep 26. PMID:17003051

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