1n4l

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(New page: 200px<br /> <applet load="1n4l" size="450" color="white" frame="true" align="right" spinBox="true" caption="1n4l, resolution 2.00&Aring;" /> '''A DNA analogue of t...)
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'''A DNA analogue of the polypurine tract of HIV-1'''<br />
'''A DNA analogue of the polypurine tract of HIV-1'''<br />
==Overview==
==Overview==
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The polypurine tract (PPT) from the HIV-1 genome is resistant to digestion, by reverse transcriptase following (-)-strand synthesis and is used to, prime (+)-strand synthesis during retroviral replication. We have, determined the crystal structure of the asymmetric DNA/DNA analog16-mer, duplex (CTTTTTAAAAGAAAAG/CTTTTCTTTTAAAAAG) comprising most of the, "visible" portion of the RNA:DNA hybrid from the polypurine tract of, HIV-1, which was previously reported in a complex with HIV-1 reverse, transcriptase. Our 16-mer completely encompasses a 10-mer DNA duplex, analog of the HIV-1 PPT. We report here a detailed analysis of our B' form, 16-mer DNA structure, including three full pure A-tracts, as well as a, comparative structural analysis with polypurine tract and other, A-tract-containing nucleic acid structures. Our analysis reveals that the, polypurine tract structures share structural features despite being, different nucleic acid forms (i.e. DNA:DNA versus RNA:DNA). In addition, the previously reported A-tract-containing DNA molecules bound to, topoisomerase I are remarkably similar to our polypurine tract 16-mer, structure. On the basis of our analysis, we suggest that the specific, topology of long pure A-tracts is remarkably comparable across a wide, array of biological environments.
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The polypurine tract (PPT) from the HIV-1 genome is resistant to digestion by reverse transcriptase following (-)-strand synthesis and is used to prime (+)-strand synthesis during retroviral replication. We have determined the crystal structure of the asymmetric DNA/DNA analog16-mer duplex (CTTTTTAAAAGAAAAG/CTTTTCTTTTAAAAAG) comprising most of the "visible" portion of the RNA:DNA hybrid from the polypurine tract of HIV-1, which was previously reported in a complex with HIV-1 reverse transcriptase. Our 16-mer completely encompasses a 10-mer DNA duplex analog of the HIV-1 PPT. We report here a detailed analysis of our B' form 16-mer DNA structure, including three full pure A-tracts, as well as a comparative structural analysis with polypurine tract and other A-tract-containing nucleic acid structures. Our analysis reveals that the polypurine tract structures share structural features despite being different nucleic acid forms (i.e. DNA:DNA versus RNA:DNA). In addition, the previously reported A-tract-containing DNA molecules bound to topoisomerase I are remarkably similar to our polypurine tract 16-mer structure. On the basis of our analysis, we suggest that the specific topology of long pure A-tracts is remarkably comparable across a wide array of biological environments.
==About this Structure==
==About this Structure==
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1N4L 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=1N4L OCA].
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1N4L 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=1N4L 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.]]
[[Category: Pflomm, M.]]
[[Category: Pflomm, M.]]
[[Category: mmlv rt; polypurine tract; hiv-1; asymmetric dna; protein-dna complex]]
[[Category: mmlv rt; polypurine tract; hiv-1; asymmetric dna; protein-dna complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Thu Nov 8 14:21:14 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:02:17 2008''

Revision as of 12:02, 21 February 2008


1n4l, resolution 2.00Å

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A DNA analogue of the polypurine tract of HIV-1

Overview

The polypurine tract (PPT) from the HIV-1 genome is resistant to digestion by reverse transcriptase following (-)-strand synthesis and is used to prime (+)-strand synthesis during retroviral replication. We have determined the crystal structure of the asymmetric DNA/DNA analog16-mer duplex (CTTTTTAAAAGAAAAG/CTTTTCTTTTAAAAAG) comprising most of the "visible" portion of the RNA:DNA hybrid from the polypurine tract of HIV-1, which was previously reported in a complex with HIV-1 reverse transcriptase. Our 16-mer completely encompasses a 10-mer DNA duplex analog of the HIV-1 PPT. We report here a detailed analysis of our B' form 16-mer DNA structure, including three full pure A-tracts, as well as a comparative structural analysis with polypurine tract and other A-tract-containing nucleic acid structures. Our analysis reveals that the polypurine tract structures share structural features despite being different nucleic acid forms (i.e. DNA:DNA versus RNA:DNA). In addition, the previously reported A-tract-containing DNA molecules bound to topoisomerase I are remarkably similar to our polypurine tract 16-mer structure. On the basis of our analysis, we suggest that the specific topology of long pure A-tracts is remarkably comparable across a wide array of biological environments.

About this Structure

1N4L 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

Staying straight with A-tracts: a DNA analog of the HIV-1 polypurine tract., Cote ML, Pflomm M, Georgiadis MM, J Mol Biol. 2003 Jun 27;330(1):57-74. PMID:12818202

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