7BVQ
Structure of human beta1 adrenergic receptor bound to carazolol
Summary for 7BVQ
Entry DOI | 10.2210/pdb7bvq/pdb |
Related PRD ID | PRD_900001 |
Descriptor | Endolysin,Beta-1 adrenergic receptor chimera, alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose, CHOLESTEROL, ... (10 entities in total) |
Functional Keywords | g protein coupled receptor, membrane protein, signaling protein |
Biological source | Enterobacteria phage T4 More |
Total number of polymer chains | 2 |
Total formula weight | 108350.98 |
Authors | Xu, X.,Kaindl, J.,Clark, M.,Hubner, H.,Hirata, K.,Sunahara, R.,Gmeiner, P.,Kobilka, B.K.,Liu, X. (deposition date: 2020-04-11, release date: 2020-12-02, Last modification date: 2024-10-30) |
Primary citation | Xu, X.,Kaindl, J.,Clark, M.J.,Hubner, H.,Hirata, K.,Sunahara, R.K.,Gmeiner, P.,Kobilka, B.K.,Liu, X. Binding pathway determines norepinephrine selectivity for the human beta 1 AR over beta 2 AR. Cell Res., 31:569-579, 2021 Cited by PubMed Abstract: Beta adrenergic receptors (βARs) mediate physiologic responses to the catecholamines epinephrine and norepinephrine released by the sympathetic nervous system. While the hormone epinephrine binds βAR and βAR with similar affinity, the smaller neurotransmitter norepinephrine is approximately tenfold selective for the βAR. To understand the structural basis for this physiologically important selectivity, we solved the crystal structures of the human βAR bound to an antagonist carazolol and different agonists including norepinephrine, epinephrine and BI-167107. Structural comparison revealed that the catecholamine-binding pockets are identical between βAR and βAR, but the extracellular vestibules have different shapes and electrostatic properties. Metadynamics simulations and mutagenesis studies revealed that these differences influence the path norepinephrine takes to the orthosteric pocket and contribute to the different association rates and thus different affinities. PubMed: 33093660DOI: 10.1038/s41422-020-00424-2 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.5 Å) |
Structure validation
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