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1EDR

MOLECULAR AND CRYSTAL STRUCTURE OF D(CGCGMO6AATTCGCG) AT 1.6 ANGSTROM

Summary for 1EDR
Entry DOI10.2210/pdb1edr/pdb
Descriptor5'-D(*CP*GP*CP*GP*(A47)AP*AP*TP*TP*CP*GP*CP*G)-3', MAGNESIUM ION, SPERMINE, ... (4 entities in total)
Functional Keywordsb-dna, double helix, deoxyribonucleic acid, modified nucleotide, methoxyadenosine, damaged dna, dna
Total number of polymer chains2
Total formula weight7613.48
Authors
Chatake, T.,Hikima, T.,Ono, A.,Ueno, Y.,Matsuda, A.,Takenaka, A. (deposition date: 2000-01-28, release date: 2000-02-16, Last modification date: 2024-02-07)
Primary citationChatake, T.,Hikima, T.,Ono, A.,Ueno, Y.,Matsuda, A.,Takenaka, A.
Crystallographic studies on damaged DNAs. II. N(6)-methoxyadenine can present two alternate faces for Watson-Crick base-pairing, leading to pyrimidine transition mutagenesis.
J.Mol.Biol., 294:1223-1230, 1999
Cited by
PubMed Abstract: In a previous paper, 2'-deoxy-N(6)-methoxyadenosine (mo(6)A) was shown to form a mismatch base-pair with 2'-deoxycytidine with a Watson-Crick-type geometry. To fully understand the structural basis of genetic mutations with damaged DNA, it is necessary to examine whether the methoxylated adenine residue still has the ability to form the regular Watson-Crick pairing with a thymine residue. Therefore, a DNA dodecamer with the sequence d(CGCGmo(6)AATTCGCG) has been synthesized and its crystal structure determined. The methoxylation has no significant effect on the overall DNA conformation, which is that of a standard B-form duplex. The methoxylated adenine moieties adopt the amino tautomer with an anti conformation around the C(6)-N(6) bond to the N(1) atom, and they form a Watson-Crick base-pair with thymine residues on the opposite strand, similar to an unmodified adenine residue. It is concluded that methoxylated adenine can present two alternate faces for base-pairing, thanks to the amino<-->imino tautomerism allowed by methoxylation. Based on this property, two gene transition routes are proposed.
PubMed: 10600380
DOI: 10.1006/jmbi.1999.3304
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.6 Å)
Structure validation

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数据于2025-06-25公开中

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