GPCR Conformations: Implications for Rational Drug Design
G protein-coupled receptors (GPCRs) comprise a large class of transmembrane proteins that play critical roles in both normal physiology and pathophysiology. These critical roles offer targets for therapeutic intervention, as exemplified by the substantial fraction of current pharmaceutical agents th...
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Format: | Book |
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MDPI AG,
2010-12-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_daeda5ed96fa4d6cad6fc3eba7a79ddc | ||
042 | |a dc | ||
100 | 1 | 0 | |a Abby L. Parrill |e author |
700 | 1 | 0 | |a Debra L. Bautista |e author |
245 | 0 | 0 | |a GPCR Conformations: Implications for Rational Drug Design |
260 | |b MDPI AG, |c 2010-12-01T00:00:00Z. | ||
500 | |a 10.3390/ph4010007 | ||
500 | |a 1424-8247 | ||
520 | |a G protein-coupled receptors (GPCRs) comprise a large class of transmembrane proteins that play critical roles in both normal physiology and pathophysiology. These critical roles offer targets for therapeutic intervention, as exemplified by the substantial fraction of current pharmaceutical agents that target members of this family. Tremendous contributions to our understanding of GPCR structure and dynamics have come from both indirect and direct structural characterization techniques. Key features of GPCR conformations derived from both types of characterization techniques are reviewed. | ||
546 | |a EN | ||
690 | |a G protein-coupled receptor | ||
690 | |a GPCR | ||
690 | |a structure | ||
690 | |a crystallography | ||
690 | |a NMR | ||
690 | |a modeling | ||
690 | |a Medicine | ||
690 | |a R | ||
690 | |a Pharmacy and materia medica | ||
690 | |a RS1-441 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Pharmaceuticals, Vol 4, Iss 1, Pp 7-43 (2010) | |
787 | 0 | |n http://www.mdpi.com/1424-8247/4/1/7/ | |
787 | 0 | |n https://doaj.org/toc/1424-8247 | |
856 | 4 | 1 | |u https://doaj.org/article/daeda5ed96fa4d6cad6fc3eba7a79ddc |z Connect to this object online. |