کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8410915 | 1545166 | 2009 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Computational analysis of membrane proteins: the largest class of drug targets
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موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
بیوتکنولوژی یا زیستفناوری
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چکیده انگلیسی
Given the key roles of integral membrane proteins as transporters and channels, it is necessary to understand their structures and, hence, mechanisms and regulation at the molecular level. Membrane proteins represent â¼30% of all proteins of currently sequenced genomes. Paradoxically, however, only â¼2% of crystal structures deposited in the protein data bank are of membrane proteins, and very few of these are at high resolution (better than 2Â Ã
). The great disparity between our understanding of soluble proteins and our understanding of membrane proteins is because of the practical problems of working with membrane proteins - specifically, difficulties in expression, purification and crystallization. Thus, computational modeling has been utilized extensively to make crucial advances in understanding membrane protein structure and function.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Drug Discovery Today - Volume 14, Issues 23â24, December 2009, Pages 1130-1135
Journal: Drug Discovery Today - Volume 14, Issues 23â24, December 2009, Pages 1130-1135
نویسندگان
Yalini Arinaminpathy, Ekta Khurana, Donald M. Engelman, Mark B. Gerstein,