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PDB: 5 results

7ZAU
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BU of 7zau by Molmil
Fascin-1 in complex with Nb 3E11
Descriptor: 1,2-ETHANEDIOL, DI(HYDROXYETHYL)ETHER, Fascin, ...
Authors:Burgess, S.G, Bayliss, R.
Deposit date:2022-03-22
Release date:2023-09-27
Last modified:2024-03-27
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:A nanobody inhibitor of Fascin-1 actin-bundling activity and filopodia formation.
Open Biology, 14, 2024
6I2U
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BU of 6i2u by Molmil
Aurora-A kinase domain in complex with Coenzyme A
Descriptor: Aurora kinase A, COENZYME A, DI(HYDROXYETHYL)ETHER, ...
Authors:Burgess, S.G, Bayliss, R.
Deposit date:2018-11-02
Release date:2019-10-02
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Covalent Aurora A regulation by the metabolic integrator coenzyme A.
Redox Biol, 28, 2019
4CEG
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BU of 4ceg by Molmil
Crystal structure of Aurora A 122-403 C290A, C393A bound to ADP
Descriptor: ADENOSINE-5'-DIPHOSPHATE, AURORA KINASE A, CHLORIDE ION, ...
Authors:Burgess, S.G, Bayliss, R.
Deposit date:2013-11-11
Release date:2015-01-28
Last modified:2023-12-20
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:The Structure of C290A:C393A Aurora a Provides Structural Insights Into Kinase Regulation.
Acta Crystallogr.,Sect.F, 71, 2015
5G1X
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BU of 5g1x by Molmil
Crystal structure of Aurora-A kinase in complex with N-Myc
Descriptor: ADENOSINE-5'-DIPHOSPHATE, AURORA KINASE A, MAGNESIUM ION, ...
Authors:Richards, M.W, Burgess, S.G, Bayliss, R.
Deposit date:2016-03-31
Release date:2016-11-16
Last modified:2024-10-16
Method:X-RAY DIFFRACTION (1.72 Å)
Cite:Structural Basis of N-Myc Binding by Aurora-A and its Destabilization by Kinase Inhibitors
Proc.Natl.Acad.Sci.USA, 113, 2016
5ORL
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BU of 5orl by Molmil
Crystal structure of Aurora-A kinase in complex with an allosterically binding fragment
Descriptor: ADENOSINE-5'-DIPHOSPHATE, Aurora kinase A, CHLORIDE ION, ...
Authors:McIntyre, P.J, Collins, P.M, Vrzal, L, Birchall, K, Arnold, L.H, Mpamhanga, C, Coombs, P.J, Burgess, S.G, Richards, M.W, Winter, A, Veverka, V, von Delft, F, Merritt, A, Bayliss, R.
Deposit date:2017-08-16
Release date:2017-11-01
Last modified:2017-11-29
Method:X-RAY DIFFRACTION (1.69 Å)
Cite:Characterization of Three Druggable Hot-Spots in the Aurora-A/TPX2 Interaction Using Biochemical, Biophysical, and Fragment-Based Approaches.
ACS Chem. Biol., 12, 2017

226707

数据于2024-10-30公开中

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