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The solution conformation of a carbocyclic analog of the Dickerson-Drew dodecamer: Comparison with its own X-ray structure and that of the NMR structure of the native counterpart

التفاصيل البيبلوغرافية
العنوان: The solution conformation of a carbocyclic analog of the Dickerson-Drew dodecamer: Comparison with its own X-ray structure and that of the NMR structure of the native counterpart
المؤلفون: Denisov, AY, Zamaratski, EV, Maltseva, TV, Sandstrom, A, Bekiroglu, S, Altmann, KH, Egli, M, Chattopadhyaya, J
المصدر: JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS. 16(3):547-568
مصطلحات موضوعية: NUCLEIC-ACID FRAGMENTS, B-DNA DODECAMER, RESTRAINED MOLECULAR-DYNAMICS, 500-MHZ H-1-NMR SPECTROSCOPY, PROTON COUPLING-CONSTANTS, PSEUDOROTATIONAL EQUILIBRIUM, PENTOFURANOSE MOIETY, SUGAR CONFORMATION, KARPLUS EQUATION, C-NUCLEOSIDES
الوصف: The NMR conformation of a carbocyclic analog of the Dickerson-Drew dodecamer [d(CGCGAAT*T*'CGCG)](2) containing 6'-alpha-Me carbocyclic thymidines (T*) has been determined and compared with that of its X-ray structure. The solution structure of the 6'-alp
وصف الملف: print
URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-27417
قاعدة البيانات: SwePub
الوصف
تدمد:07391102