1n37
From Proteopedia
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|PDB= 1n37 |SIZE=350|CAPTION= <scene name='initialview01'>1n37</scene> | |PDB= 1n37 |SIZE=350|CAPTION= <scene name='initialview01'>1n37</scene> | ||
|SITE= | |SITE= | ||
- | |LIGAND= <scene name='pdbligand=RSD:RESPINOMYCIN D'>RSD</scene> | + | |LIGAND= <scene name='pdbligand=DA:2'-DEOXYADENOSINE-5'-MONOPHOSPHATE'>DA</scene>, <scene name='pdbligand=DC:2'-DEOXYCYTIDINE-5'-MONOPHOSPHATE'>DC</scene>, <scene name='pdbligand=DG:2'-DEOXYGUANOSINE-5'-MONOPHOSPHATE'>DG</scene>, <scene name='pdbligand=DT:THYMIDINE-5'-MONOPHOSPHATE'>DT</scene>, <scene name='pdbligand=RSD:RESPINOMYCIN+D'>RSD</scene> |
|ACTIVITY= | |ACTIVITY= | ||
|GENE= | |GENE= | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY= | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1n37 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1n37 OCA], [http://www.ebi.ac.uk/pdbsum/1n37 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1n37 RCSB]</span> | ||
}} | }} | ||
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[[Category: Searle, M S.]] | [[Category: Searle, M S.]] | ||
[[Category: Williams, H E.L.]] | [[Category: Williams, H E.L.]] | ||
- | [[Category: RSD]] | ||
[[Category: anthracycline antibiotc]] | [[Category: anthracycline antibiotc]] | ||
[[Category: drug-dna recognition]] | [[Category: drug-dna recognition]] | ||
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[[Category: respinomycin d]] | [[Category: respinomycin d]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:24:43 2008'' |
Revision as of 19:24, 30 March 2008
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Ligands: | , , , , | ||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
NMR Solution Structure of the Anthracycline Respinomycin D Intercalation Complex with a Double Stranded DNA Molecule (AGACGTCT)2
Overview
Respinomycin D is a member of the anthracycline family of antitumour antibiotics that interact with double stranded DNA through intercalation. The clinical agents daunomycin and doxorubicin are the most well-studied of this class but have a relatively simple molecular architecture in which the pendant daunosamine sugar resides in the DNA minor groove. Respinomycin D, which belongs to the nogalamycin group of anthracyclines, possesses additional sugar residues at either end of the aglycone chromophore that modulate the biological activity but whose role in molecular recognition is unknown. We report the NMR structure of the respinomycin D-d(AGACGTCT)2 complex in solution derived from NOE restraints and molecular dynamics simulations. We show that the drug threads through the DNA double helix forming stabilising interactions in both the major and minor groove, the latter through a different binding geometry to that previously reported. The bicycloaminoglucose sugar resides in the major groove and makes specific contacts with guanine at the 5'-CpG intercalation site, however, the disaccharide attached at the C4 position plays little part in drug binding and DNA recognition and is largely solvent exposed.
About this Structure
1N37 is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.
Reference
DNA recognition by the anthracycline antibiotic respinomycin D: NMR structure of the intercalation complex with d(AGACGTCT)2., Searle MS, Maynard AJ, Williams HE, Org Biomol Chem. 2003 Jan 7;1(1):60-6. PMID:12929391
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