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7DHW
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BU of 7dhw by Molmil
Crystal structure of myosin-XI motor domain in complex with ADP-ALF4
Descriptor: ADENOSINE-5'-DIPHOSPHATE, GLYCEROL, MAGNESIUM ION, ...
Authors:Suzuki, K, Haraguchi, T, Tamanaha, M, Yoshimura, K, Imi, T, Tominaga, M, Sakayama, H, Nishiyama, T, Ito, K, Murata, T.
Deposit date:2020-11-17
Release date:2021-05-19
Last modified:2023-11-29
Method:X-RAY DIFFRACTION (2.84 Å)
Cite:Discovery of ultrafast myosin, its amino acid sequence, and structural features.
Proc.Natl.Acad.Sci.USA, 119, 2022
6LGP
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BU of 6lgp by Molmil
cryo-EM structure of TRPV3 in lipid nanodisc
Descriptor: (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate, DIUNDECYL PHOSPHATIDYL CHOLINE, Transient receptor potential cation channel subfamily V member 3
Authors:Shimada, H, Kusakizako, T, Nishizawa, T, Nureki, O.
Deposit date:2019-12-05
Release date:2020-06-24
Last modified:2024-03-27
Method:ELECTRON MICROSCOPY (3.3 Å)
Cite:The structure of lipid nanodisc-reconstituted TRPV3 reveals the gating mechanism.
Nat.Struct.Mol.Biol., 27, 2020
8JVI
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BU of 8jvi by Molmil
Structure of human TRPV4 with antagonist A2
Descriptor: Transient receptor potential cation channel subfamily V member 4,3C-GFP, [6-[[4-(2,4-dimethyl-1,3-thiazol-5-yl)-1,3-thiazol-2-yl]amino]pyridin-3-yl]-[(1~{S},5~{R})-3-[5-(trifluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[3.2.1]octan-8-yl]methanone
Authors:Fan, J, Lei, X.
Deposit date:2023-06-28
Release date:2024-05-08
Method:ELECTRON MICROSCOPY (3.21 Å)
Cite:Structural Pharmacology of TRPV4 Antagonists.
Adv Sci, 2024
8JVJ
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BU of 8jvj by Molmil
Structure of human TRPV4 with antagonist A2 and RhoA
Descriptor: Transforming protein RhoA, Transient receptor potential cation channel subfamily V member 4,3C-GFP, [6-[[4-(2,4-dimethyl-1,3-thiazol-5-yl)-1,3-thiazol-2-yl]amino]pyridin-3-yl]-[(1~{S},5~{R})-3-[5-(trifluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[3.2.1]octan-8-yl]methanone
Authors:Fan, J, Lei, X.
Deposit date:2023-06-28
Release date:2024-05-08
Method:ELECTRON MICROSCOPY (3.44 Å)
Cite:Structural Pharmacology of TRPV4 Antagonists.
Adv Sci, 2024
8JU5
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BU of 8ju5 by Molmil
Structure of human TRPV4 with antagonist A1
Descriptor: 4-[(3~{S},4~{S})-4-(aminomethyl)-1-(5-chloranylpyridin-2-yl)sulfonyl-4-oxidanyl-pyrrolidin-3-yl]oxy-2-fluoranyl-benzenecarbonitrile, Transient receptor potential cation channel subfamily V member 4,3C-GFP
Authors:Fan, J, Lei, X.
Deposit date:2023-06-24
Release date:2024-05-08
Method:ELECTRON MICROSCOPY (3.74 Å)
Cite:Structural Pharmacology of TRPV4 Antagonists.
Adv Sci, 2024
8JU6
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BU of 8ju6 by Molmil
Structure of human TRPV4 with antagonist GSK279
Descriptor: 1-({(5S,7S)-3-[5-(2-hydroxypropan-2-yl)pyrazin-2-yl]-7-methyl-2-oxo-1-oxa-3-azaspiro[4.5]decan-7-yl}methyl)-1H-benzimidazole-6-carbonitrile, Transient receptor potential cation channel subfamily V member 4,3C-GFP
Authors:Fan, J, Lei, X.
Deposit date:2023-06-24
Release date:2024-05-08
Method:ELECTRON MICROSCOPY (3.45 Å)
Cite:Structural Pharmacology of TRPV4 Antagonists.
Adv Sci, 2024

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PDB entries from 2024-05-15

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