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2L4J
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BU of 2l4j by Molmil
Yap ww2
Descriptor: Yes-associated protein 2 (YAP2)
Authors:Webb, C, Upadhyay, A, Furutani-Seiki, M, Bagby, S.
Deposit date:2010-10-07
Release date:2010-11-03
Last modified:2024-05-01
Method:SOLUTION NMR
Cite:Structural Features and Ligand Binding Properties of Tandem WW Domains from YAP and TAZ, Nuclear Effectors of the Hippo Pathway.
Biochemistry, 50, 2011
4K7C
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BU of 4k7c by Molmil
Crystal structure of pepw from lactobacillus rhamnosis hn001 (dr20) determined as the selenomet derivative
Descriptor: Aminopeptidase C, GLYCEROL
Authors:Webby, C, Knapp, K.M, Anderson, B.F, Norris, G.E.
Deposit date:2013-04-16
Release date:2013-06-19
Last modified:2024-11-27
Method:X-RAY DIFFRACTION (1.66 Å)
Cite:Crystal structure of pepw from lactobacillus rhamnosis hn001 (dr20) determined as the selenomet derivative
TO BE PUBLISHED
9MQJ
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BU of 9mqj by Molmil
Locally-refined Inactive Mu-Opioid Receptor with Nb6M, NabFab, and isoquinuclidine compound #020_E1
Descriptor: Mu-type opioid receptor, methyl (1S,3R,4S,6S,8M)-2-[(1-ethyl-1H-pyrazol-4-yl)methyl]-8-(3-hydroxyphenyl)-3,4-dimethyl-2-azabicyclo[2.2.2]oct-7-ene-6-carboxylate
Authors:Kim, J.Y, Vigneron, S.F, Billesbolle, C, Manglik, A, Shoichet, B.K.
Deposit date:2025-01-03
Release date:2025-02-12
Method:ELECTRON MICROSCOPY (3.23 Å)
Cite:Docking 14 million virtual isoquinuclidines against the mu and kappa opioid receptors reveals dual antagonists-inverse agonists with reduced withdrawal effects.
Biorxiv, 2025
9MQK
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BU of 9mqk by Molmil
Inactive Kappa-Opioid Receptor with Nb6M, NabFab, and isoquinuclidine compound #020_E1
Descriptor: Kappa-Opioid Receptor, NabFab Heavy Chain, NabFab Light Chain, ...
Authors:Kim, J.Y, Vigneron, S.F, Billesbolle, C, Manglik, A, Shoichet, B.K.
Deposit date:2025-01-03
Release date:2025-02-12
Last modified:2025-03-12
Method:ELECTRON MICROSCOPY (3.18 Å)
Cite:Docking 14 million virtual isoquinuclidines against the mu and kappa opioid receptors reveals dual antagonists-inverse agonists with reduced withdrawal effects.
Biorxiv, 2025
9MQH
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BU of 9mqh by Molmil
Inactive Mu-Opioid Receptor with Nb6M, NabFab, and isoquinuclidine compound #33
Descriptor: Mu-type opioid receptor
Authors:Kim, J.Y, Vigneron, S.F, Billesbolle, C, Manglik, A, Shoichet, B.K.
Deposit date:2025-01-03
Release date:2025-02-12
Method:ELECTRON MICROSCOPY (3.9 Å)
Cite:Docking 14 million virtual isoquinuclidines against the mu and kappa opioid receptors reveals dual antagonists-inverse agonists with reduced withdrawal effects.
Biorxiv, 2025
9MQL
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BU of 9mql by Molmil
Locally-Refined Inactive Kappa-Opioid Receptor with Nb6M, NabFab, and isoquinuclidine compound #020_E1
Descriptor: Kappa-Opioid Receptor, methyl (1S,3R,4S,6S,8M)-2-[(1-ethyl-1H-pyrazol-4-yl)methyl]-8-(3-hydroxyphenyl)-3,4-dimethyl-2-azabicyclo[2.2.2]oct-7-ene-6-carboxylate
Authors:Kim, J.Y, Vigneron, S.F, Billesbolle, C, Manglik, A, Shoichet, B.K.
Deposit date:2025-01-03
Release date:2025-02-12
Last modified:2025-03-12
Method:ELECTRON MICROSCOPY (2.96 Å)
Cite:Docking 14 million virtual isoquinuclidines against the mu and kappa opioid receptors reveals dual antagonists-inverse agonists with reduced withdrawal effects.
Biorxiv, 2025
9MQI
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BU of 9mqi by Molmil
Inactive Mu-Opioid Receptor with Nb6M, NabFab, and isoquinuclidine compound #020_E1
Descriptor: Mu-type opioid receptor, NabFab Heavy Chain, NabFab Light Chain, ...
Authors:Kim, J.Y, Vigneron, S.F, Billesbolle, C, Manglik, A, Shoichet, B.K.
Deposit date:2025-01-03
Release date:2025-02-12
Method:ELECTRON MICROSCOPY (3.3 Å)
Cite:Docking 14 million virtual isoquinuclidines against the mu and kappa opioid receptors reveals dual antagonists-inverse agonists with reduced withdrawal effects.
Biorxiv, 2025
8SUO
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BU of 8suo by Molmil
BA.2/AZD1061/AZD3152 structure analysis
Descriptor: AZD1061 heavy chain, AZD1061 light chain, AZD3152 heavy chain, ...
Authors:Oganesyan, V, van Dyk, N, Dippel, A, Barnes, A, O'Connor, E.
Deposit date:2023-05-12
Release date:2024-05-15
Last modified:2024-11-27
Method:X-RAY DIFFRACTION (3.3 Å)
Cite:AZD3152 neutralizes SARS-CoV-2 historical and contemporary variants and is protective in hamsters and well tolerated in adults.
Sci Transl Med, 16, 2024

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