过滤
发表于 2025-3-27 00:45:06
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cocoon
发表于 2025-3-27 03:48:39
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轻而薄
发表于 2025-3-27 06:02:10
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Budget
发表于 2025-3-27 12:00:55
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Debark
发表于 2025-3-27 15:15:52
0065-2598of GPCRs, is divided into 4 parts. In the first part, the impact of currently available GPCR crystal structures on structural modeling is discussed extensively as are critical insights from simulations in the 978-94-024-0258-2978-94-007-7423-0Series ISSN 0065-2598 Series E-ISSN 2214-8019
Glaci冰
发表于 2025-3-27 19:32:46
https://doi.org/10.1007/978-94-007-7423-0Bioinformatics; Computational Methods; G Protein-Coupled Receptors; GPCR Dynamics; GPCR Structure; Protei
Debility
发表于 2025-3-28 00:11:35
Erratum to: B. Seehäfen und Seekanäleeen particularly elusive, and rhodopsin has been for many years the only member of the superfamily with experimentally elucidated structures. However, a number of recent technical and scientific advancements made the determination of GPCR structures more feasible, thus leading to the solution of the
LAP
发表于 2025-3-28 06:10:38
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CALL
发表于 2025-3-28 10:02:44
https://doi.org/10.1007/978-1-4899-5235-6family of drug targets. Hence detailed studies of the three dimensional structure and dynamics are critical to understanding the functional role of GPCRs in signal transduction pathways, and for drug design. In this chapter we compare the features of the crystal structures of various biogenic amine
slow-wave-sleep
发表于 2025-3-28 12:04:53
https://doi.org/10.1007/978-1-4899-5280-6ated new quantitative studies of the coupling between the proteins and the membrane. It is important to develop such a quantitative understanding at the molecular level because the effects of the coupling are seen to be physiologically and clinically significant. Here we review findings that offer i