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3VTE
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CRYSTAL STRUCTURE OF TETRAHYDROCANNABINOLIC ACID SYNTHASE FROM CANNABIS SATIVA
Descriptor:Tetrahydrocannabinolic acid synthase, N-ACETYL-D-GLUCOSAMINE, FLAVIN-ADENINE DINUCLEOTIDE
Authors:Shoyama, Y., Tamada, T., Kurihara, K., Takeuchi, A., Taura, F., Arai, S., Blaber, M., Shoyama, Y., Morimoto, S., Kuroki, R.
Deposit date:2012-05-28
Release date:2012-07-25
Last modified:2014-04-30
Method:X-RAY DIFFRACTION (2.75 Å)
Cite:Structure and function of 1-tetrahydrocannabinolic acid (THCA) synthase, the enzyme controlling the psychoactivity of Cannabis sativa
J.Mol.Biol., 423, 2012
5Y25
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EGFR KINASE DOMAIN MUTANT (T790M/L858R) WITH COVALENT LIGAND NS-062
Descriptor:Epidermal growth factor receptor, (2R)-N-[4-[(3-chloranyl-4-fluoranyl-phenyl)amino]-7-(3-morpholin-4-ylpropoxy)quinazolin-6-yl]-1-(2-fluoranylethanoyl)pyrrolidine-2-carboxamide
Authors:Shiroishi, M., Abe, Y., Caaveiro, J.M.M., Sakamoto, S., Morimoto, S., Fuchida, H., Shindo, N., Ojida, A.
Deposit date:2017-07-24
Release date:2018-07-25
Method:X-RAY DIFFRACTION (3.102 Å)
Cite:EGFR kinase domain mutant (T790M/L858R) with covalent ligand NS-062
To Be Published
1RDV
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RUBREDOXIN FROM DESULFOVIBRIO VULGARIS MIYAZAKI F, TRIGONAL CRYSTAL FORM
Descriptor:RUBREDOXIN, FE (III) ION
Authors:Higuchi, Y., Yasuoka, N.
Deposit date:1998-09-30
Release date:1999-05-18
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2 Å)
Cite:Structure determination of rubredoxin from Desulfovibrio vulgaris Miyazaki F in two crystal forms.
Acta Crystallogr.,Sect.D, 55, 1999
2RDV
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RUBREDOXIN FROM DESULFOVIBRIO VULGARIS MIYAZAKI F, MONOCLINIC CRYSTAL FORM
Descriptor:RUBREDOXIN, FE (III) ION
Authors:Higuchi, Y., Yasuoka, N.
Deposit date:1998-10-07
Release date:1999-05-18
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structure determination of rubredoxin from Desulfovibrio vulgaris Miyazaki F in two crystal forms.
Acta Crystallogr.,Sect.D, 55, 1999
6M95
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STRUCTURE-BASED DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF IMIDAZO[4,5-B]PYRIDINE-2-ONE BASED P38 MAP KINASE INHIBITORS BY SCAFFOLD HOPPING: COMPOUND 1
Descriptor:Mitogen-activated protein kinase 14, (4-benzylpiperidin-1-yl)[2-methoxy-4-(methylsulfanyl)phenyl]methanone
Authors:Lane, W., Okada, K.
Deposit date:2018-08-22
Release date:2019-04-17
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Structure-based Design, Synthesis, and Biological Evaluation of Imidazo[4,5-b]pyridin-2-one-based p38 MAP Kinase Inhibitors: Part 1.
ChemMedChem, 2019
6M9L
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STRUCTURE-BASED DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF IMIDAZO[4,5-B]PYRIDINE-2-ONE BASED P38 MAP KINASE INHIBITORS BY SCAFFOLD HOPPING - COMPOUND 10
Descriptor:Mitogen-activated protein kinase 14, 3-benzyl-6-[(2,4-difluorophenyl)amino]-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
Authors:Lane, W., Okada, K.
Deposit date:2018-08-23
Release date:2019-04-17
Method:X-RAY DIFFRACTION (2.45 Å)
Cite:Structure-based Design, Synthesis, and Biological Evaluation of Imidazo[4,5-b]pyridin-2-one-based p38 MAP Kinase Inhibitors: Part 1.
ChemMedChem, 2019