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Atomistry » Sodium » PDB 6h6r-6hj3 » 6h7o | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Sodium » PDB 6h6r-6hj3 » 6h7o » |
Sodium in PDB 6h7o: Activated Turkey BETA1 Adrenoceptor with Bound Weak Partial Agonist Cyanopindolol and Nanobody NB6B9Protein crystallography data
The structure of Activated Turkey BETA1 Adrenoceptor with Bound Weak Partial Agonist Cyanopindolol and Nanobody NB6B9, PDB code: 6h7o
was solved by
T.Warne,
P.C.Edwards,
A.S.Dore,
A.G.W.Leslie,
C.G.Tate,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Sodium Binding Sites:
The binding sites of Sodium atom in the Activated Turkey BETA1 Adrenoceptor with Bound Weak Partial Agonist Cyanopindolol and Nanobody NB6B9
(pdb code 6h7o). This binding sites where shown within
5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the Activated Turkey BETA1 Adrenoceptor with Bound Weak Partial Agonist Cyanopindolol and Nanobody NB6B9, PDB code: 6h7o: Jump to Sodium binding site number: 1; 2; Sodium binding site 1 out of 2 in 6h7oGo back to Sodium Binding Sites List in 6h7o
Sodium binding site 1 out
of 2 in the Activated Turkey BETA1 Adrenoceptor with Bound Weak Partial Agonist Cyanopindolol and Nanobody NB6B9
Mono view Stereo pair view
Sodium binding site 2 out of 2 in 6h7oGo back to Sodium Binding Sites List in 6h7o
Sodium binding site 2 out
of 2 in the Activated Turkey BETA1 Adrenoceptor with Bound Weak Partial Agonist Cyanopindolol and Nanobody NB6B9
Mono view Stereo pair view
Reference:
T.Warne,
P.C.Edwards,
A.S.Dore,
A.G.W.Leslie,
C.G.Tate.
Molecular Basis For High-Affinity Agonist Binding in Gpcrs. Science V. 364 775 2019.
Page generated: Tue Oct 8 09:14:48 2024
ISSN: ESSN 1095-9203 PubMed: 31072904 DOI: 10.1126/SCIENCE.AAU5595 |
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