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4F3L
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CRYSTAL STRUCTURE OF THE HETERODIMERIC CLOCK:BMAL1 TRANSCRIPTIONAL ACTIVATOR COMPLEX
Descriptor:BMAL1b, Circadian locomoter output cycles protein kaput
Authors:Huang, N., Chelliah, Y., Shan, Y., Taylor, C., Yoo, S., Partch, C., Green, C.B., Zhang, H., Takahashi, J.
Deposit date:2012-05-09
Release date:2012-06-06
Last modified:2018-12-05
Method:X-RAY DIFFRACTION (2.268 Å)
Cite:Crystal structure of the heterodimeric CLOCK:BMAL1 transcriptional activator complex.
Science, 337, 2012
3AQJ
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CRYSTAL STRUCTURE OF A C-TERMINAL DOMAIN OF THE BACTERIOPHAGE P2 TAIL SPIKE PROTEIN, GPV
Descriptor:Baseplate assembly protein V, FE (II) ION, CHLORIDE ION, ...
Authors:Takeda, S., Yamashita, E., Nakagawa, A.
Deposit date:2010-11-06
Release date:2011-08-10
Last modified:2012-04-25
Method:X-RAY DIFFRACTION (1.27 Å)
Cite:The host-binding domain of the P2 phage tail spike reveals a trimeric iron-binding structure
Acta Crystallogr.,Sect.F, 67, 2011
3WA4
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GRB2 SH2 DOMAIN/CD28-DERIVED PEPTIDE COMPLEX
Descriptor:Growth factor receptor-bound protein 2, T-cell-specific surface glycoprotein CD28, CADMIUM ION, ...
Authors:Higo, K., Oda, M., Ito, N.
Deposit date:2013-04-23
Release date:2014-02-26
Method:X-RAY DIFFRACTION (1.35 Å)
Cite:High Resolution Crystal Structure of the Grb2 SH2 Domain with a Phosphopeptide Derived from CD28
Plos One, 8, 2013
5YJM
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HUMAN CHYMASE IN COMPLEX WITH 7-OXO-3-(PHENOXYIMINO)-1,4-DIAZEPANE DERIVATIVE
Descriptor:human chymase, N-ACETYL-D-GLUCOSAMINE, ZINC ION, ...
Authors:Sugawara, H.
Deposit date:2017-10-11
Release date:2017-12-27
Last modified:2018-01-17
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structure-based design, synthesis, and binding mode analysis of novel and potent chymase inhibitors
Bioorg. Med. Chem. Lett., 28, 2018
5YJP
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HUMAN CHYMASE IN COMPLEX WITH 3-(ETHOXYIMINO)-7-OXO-1,4-DIAZEPANE DERIVATIVE
Descriptor:human chymase, N-ACETYL-D-GLUCOSAMINE, ZINC ION, ...
Authors:Sugawara, H.
Deposit date:2017-10-11
Release date:2017-12-27
Last modified:2018-01-17
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Structure-based design, synthesis, and binding mode analysis of novel and potent chymase inhibitors
Bioorg. Med. Chem. Lett., 28, 2018
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