1d33

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==Formaldehyde cross-links daunorubicin and DNA efficiently: HPLC and X-RAY diffraction studies==
==Formaldehyde cross-links daunorubicin and DNA efficiently: HPLC and X-RAY diffraction studies==
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<StructureSection load='1d33' size='340' side='right' caption='[[1d33]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
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<StructureSection load='1d33' size='340' side='right'caption='[[1d33]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[1d33]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1D33 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1D33 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[1d33]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1D33 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1D33 FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=DM1:DAUNOMYCIN'>DM1</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene><br>
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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]] 1.5&#8491;</td></tr>
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<tr><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=G49:N2-METHYL-2-DEOXY-GUANOSINE-5-MONOPHOSPHATE'>G49</scene></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=DM1:DAUNOMYCIN'>DM1</scene>, <scene name='pdbligand=G49:N2-METHYL-2-DEOXY-GUANOSINE-5-MONOPHOSPHATE'>G49</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
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<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1d33 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1d33 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1d33 RCSB], [http://www.ebi.ac.uk/pdbsum/1d33 PDBsum]</span></td></tr>
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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=1d33 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1d33 OCA], [https://pdbe.org/1d33 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1d33 RCSB], [https://www.ebi.ac.uk/pdbsum/1d33 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1d33 ProSAT]</span></td></tr>
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<table>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Formaldehyde (HCHO) cross-links the anticancer drug daunorubicin (DAU) to DNA efficiently. When DAU is mixed with DNA hexamers, d(CGCGCG) and d(CGTDCG), in the presence of HCHO, stable covalent adducts of DNA are formed, as shown by the HPLC analyses. The major adducts are identical with the materials in the respective crystals which can be readily obtained from the 1:1 mixture of DAU-d(CGCGCG) and DAU-d(CGTDCG) plus HCHO, but not from the solution without HCHO. The high-resolution (1.5 A) X-ray crystal structure of those adducts shows unambiguously that they contain a covalent methylene bridge between the N3' of daunosamine and the N2 of the guanine or 2-aminoadenine. The perfect juxtaposition of the two amino groups in the minor groove of the complex provides a template for an efficient addition of HCHO. The methylene bridge does not perturb the conformation of the drug-DNA complex, when compared to the structure of DAU-d(CGTACG). The results suggest new approaches for synthesizing a new type of potential anticancer drug by attaching a reactive (e.g., alkylating) functional group at the N3' amino position of daunorubicin/doxorubicin. The stable drug-DNA adduct may be useful as probes for other biological studies.
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Formaldehyde cross-links daunorubicin and DNA efficiently: HPLC and X-ray diffraction studies.,Wang AH, Gao YG, Liaw YC, Li YK Biochemistry. 1991 Apr 23;30(16):3812-5. PMID:2018756<ref>PMID:2018756</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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== References ==
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<references/>
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Gao, Y G.]]
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[[Category: Large Structures]]
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[[Category: Li, Y K.]]
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[[Category: Gao Y-G]]
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[[Category: Liaw, Y C.]]
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[[Category: Li Y-K]]
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[[Category: Wang, A H.J.]]
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[[Category: Liaw Y-C]]
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[[Category: Complexed with drug]]
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[[Category: Wang AH-J]]
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[[Category: Dna]]
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[[Category: Double helix]]
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[[Category: Modified]]
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[[Category: Right handed dna]]
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Formaldehyde cross-links daunorubicin and DNA efficiently: HPLC and X-RAY diffraction studies

PDB ID 1d33

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