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4L6Q
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BU of 4l6q by Molmil
ROCK2 in complex with benzoxaborole
Descriptor: 6-[4-(aminomethyl)-2-fluorophenoxy]-2,1-benzoxaborol-1(3H)-ol, Rho-associated protein kinase 2
Authors:Rock, F, Jarnagin, K.
Deposit date:2013-06-12
Release date:2013-10-02
Last modified:2024-02-28
Method:X-RAY DIFFRACTION (2.79 Å)
Cite:Linking phenotype to kinase: identification of a novel benzoxaborole hinge-binding motif for kinase inhibition and development of high-potency rho kinase inhibitors.
J.Pharmacol.Exp.Ther., 347, 2013
5K6J
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BU of 5k6j by Molmil
Human Phospodiesterase 4B in complex with pyridyloxy-benzoxaborole based inhibitor
Descriptor: 1,2-ETHANEDIOL, 6-[[7,7-bis(oxidanyl)-8-oxa-7-boranuidabicyclo[4.3.0]nona-1(6),2,4-trien-3-yl]oxy]-5-chloranyl-2-(4-oxidanylidenepentoxy)pyridine-3-carbonitrile, MAGNESIUM ION, ...
Authors:Rock, F.L, Zhou, Y, Sullivan, D.
Deposit date:2016-05-24
Release date:2017-05-31
Last modified:2024-03-06
Method:X-RAY DIFFRACTION (1.86 Å)
Cite:To be published
To Be Published
3O0J
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BU of 3o0j by Molmil
PDE4B In complex with ligand an2898
Descriptor: 1,2-ETHANEDIOL, 4-[(1-hydroxy-1,3-dihydro-2,1-benzoxaborol-5-yl)oxy]benzene-1,2-dicarbonitrile, MAGNESIUM ION, ...
Authors:Alley, M.R.K, Zhou, Y.
Deposit date:2010-07-19
Release date:2011-08-10
Last modified:2024-02-21
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:Boron-based phosphodiesterase inhibitors show novel binding of boron to PDE4 bimetal center.
Febs Lett., 586, 2012
1IRK
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BU of 1irk by Molmil
CRYSTAL STRUCTURE OF THE TYROSINE KINASE DOMAIN OF THE HUMAN INSULIN RECEPTOR
Descriptor: ETHYL MERCURY ION, INSULIN RECEPTOR TYROSINE KINASE DOMAIN
Authors:Hubbard, S.R, Wei, L, Ellis, L, Hendrickson, W.A.
Deposit date:1995-01-02
Release date:1995-02-27
Last modified:2024-02-07
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Crystal structure of the tyrosine kinase domain of the human insulin receptor.
Nature, 372, 1994

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