1d37

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(New page: 200px<br /><applet load="1d37" size="450" color="white" frame="true" align="right" spinBox="true" caption="1d37, resolution 1.800&Aring;" /> '''INFLUENCE OF AGLYCO...)
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[[Image:1d37.gif|left|200px]]<br /><applet load="1d37" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1d37, resolution 1.800&Aring;" />
 
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'''INFLUENCE OF AGLYCONE MODIFICATIONS ON THE BINDING OF ANTHRACYCLINE DRUGS TO DNA: THE MOLECULAR STRUCTURE OF IDARUBICIN AND 4-O-DEMETHYL-11-DEOXYDOXORUBICIN COMPLEXED TO D(CGATCG)'''<br />
 
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==Overview==
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==INFLUENCE OF AGLYCONE MODIFICATIONS ON THE BINDING OF ANTHRACYCLINE DRUGS TO DNA: THE MOLECULAR STRUCTURE OF IDARUBICIN AND 4-O-DEMETHYL-11-DEOXYDOXORUBICIN COMPLEXED TO D(CGATCG)==
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X-ray diffraction analyses of the complexes between two anthracycline, antitumor compounds, idarubicin (IDR) and 4-O-demethyl-11-deoxydoxorubicin, (ddDOX), with the DNA hexamer d(CGATCG) provided the detailed, three-dimensional molecular structures at 1.7 A and 1.8 A resolution, respectively. Their structures have been refined with the constrained, refinement procedure to final R-factors of 0.188 (1724 reflections for, IDR) and 0.179 (1247 reflections for ddDOX). The overall structures of, both complexes are similar to those of the previously studied DAU- and, DOX-DNA complexes. In both complexes, two IDR (and ddDOX) molecules bind, to the DNA hexamer double helix with the elongated aglycone chromophore, intercalated between the CpG steps at both ends of the helix. The aglycone, chromophore spans the GC Watson-Crick base pairs with its amino sugar, lying in the minor groove where little structural difference is seen, compared with the daunorubicin-d(CGATCG) and doxorubicin-d(CGATCG), complexes. In contrast, the missing C4 methoxy of IDR and the missing, methyl group at the O4 position of ddDOX result in a different binding, surface in the major groove. The O4 hydroxyl group is capable of receiving, and/or donating a hydrogen bond to proteins that bind to the drug-DNA, complex. The missing O11 hydroxyl group in ring B creates an empty space, in the intercalation cavity between the two GC base pairs, which appears, to affect the stacking interactions between the aglycone and the DNA base, pairs. Those structural changes in the major groove of the drug-DNA, complexes due to the modifications of the aglycone chromophore may be, responsible in part for the difference in their biological activities.
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<StructureSection load='1d37' size='340' side='right'caption='[[1d37]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
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== Structural highlights ==
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==About this Structure==
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<table><tr><td colspan='2'>[[1d37]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1D37 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1D37 FirstGlance]. <br>
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1D37 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with DM4 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1D37 OCA].
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=DM4:1-O-DEMETHYL-6-DEOXYDOXORUBICIN'>DM4</scene></td></tr>
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==Reference==
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1d37 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1d37 OCA], [https://pdbe.org/1d37 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1d37 RCSB], [https://www.ebi.ac.uk/pdbsum/1d37 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1d37 ProSAT]</span></td></tr>
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Influence of aglycone modifications on the binding of anthracycline drugs to DNA: the molecular structure of idarubicin and 4-O-demethyl-11-deoxydoxorubicin complexed to d(CGATCG)., Gao YG, Wang AH, Anticancer Drug Des. 1991 Jul;6(3):137-49. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=1872945 1872945]
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</table>
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[[Category: Protein complex]]
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__TOC__
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[[Category: Gao, Y.G.]]
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</StructureSection>
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[[Category: Wang, A.H.J.]]
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[[Category: Large Structures]]
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[[Category: DM4]]
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[[Category: Gao Y-G]]
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[[Category: complexed with drug]]
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[[Category: Wang AH-J]]
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[[Category: double helix]]
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[[Category: right handed dna]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:23:05 2007''
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Current revision

INFLUENCE OF AGLYCONE MODIFICATIONS ON THE BINDING OF ANTHRACYCLINE DRUGS TO DNA: THE MOLECULAR STRUCTURE OF IDARUBICIN AND 4-O-DEMETHYL-11-DEOXYDOXORUBICIN COMPLEXED TO D(CGATCG)

PDB ID 1d37

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