8VT8
 
 | | UIC-13-BIF-A4Dab NBD-Cl binding | | 分子名称: | 4-chloro-7-nitrobenzofurazan, ACETONITRILE, UIC-13-BIF-A4Dab-NBD-Cl | | 著者 | Ganatra, P. | | 登録日 | 2024-01-26 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.53 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VW7
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8VPS
 | | UIC-12-BPE extension of UIC-1 | | 分子名称: | DIMETHYLFORMAMIDE, UIC-12-BPE | | 著者 | Ganatra, P. | | 登録日 | 2024-01-16 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VPX
 | | UIC-10-BPE extension of UIC-1 | | 分子名称: | UIC-10-BPE | | 著者 | Ganatra, P. | | 登録日 | 2024-01-17 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.451 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VW8
 | | UIC-13-BPE-AgNO3 silver binding with UIC-13-BPE | | 分子名称: | NITRATE ION, SILVER ION, UIC-13-BPE-AgNO3 silver binding with UIC-13-BPE | | 著者 | Ganatra, P. | | 登録日 | 2024-01-31 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.2 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VQ0
 | | UIC-13-MER extension of UIC-1 | | 分子名称: | METHANOL, UIC-13-MER | | 著者 | Ganatra, P. | | 登録日 | 2024-01-17 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.31 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VPD
 | | UIC-11-BIF extension of UIC-1 | | 分子名称: | ACETONITRILE, UIC-11-BIF | | 著者 | Ganatra, P. | | 登録日 | 2024-01-16 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.2 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VPY
 | | UIC-16-MER extension of UIC-1 | | 分子名称: | METHANOL, UIC-16-MER | | 著者 | Ganatra, P. | | 登録日 | 2024-01-17 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.21 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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8VPZ
 | | UIC-1-BPE1MER mutation of UIC-1-cap | | 分子名称: | METHANOL, UIC-1-BPE1MER | | 著者 | Ganatra, P. | | 登録日 | 2024-01-17 | | 公開日 | 2024-08-07 | | 実験手法 | X-RAY DIFFRACTION (1.04 Å) | | 主引用文献 | Diverse Proteomimetic Frameworks via Rational Design of pi-Stacking Peptide Tectons
To Be Published
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1AX9
 | | ACETYLCHOLINESTERASE COMPLEXED WITH EDROPHONIUM, LAUE DATA | | 分子名称: | ACETYLCHOLINESTERASE, EDROPHONIUM ION | | 著者 | Raves, M.L, Ravelli, R.B.G, Sussman, J.L, Harel, M, Silman, I. | | 登録日 | 1997-11-03 | | 公開日 | 1998-02-11 | | 最終更新日 | 2023-08-02 | | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | | 主引用文献 | Static Laue diffraction studies on acetylcholinesterase.
Acta Crystallogr.,Sect.D, 54, 1998
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4I10
 | | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates | | 分子名称: | 2-{(1S)-1-[(6-chloro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)amino]-2-phenylethyl}pyrido[4,3-d]pyrimidin-4(1H)-one, Beta-secretase 1, ZINC ION | | 著者 | Lougheed, J.C, Brecht, E, Yao, N.H. | | 登録日 | 2012-11-19 | | 公開日 | 2013-03-06 | | 最終更新日 | 2013-04-24 | | 実験手法 | X-RAY DIFFRACTION (2.07 Å) | | 主引用文献 | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates.
Bioorg.Med.Chem.Lett., 23, 2013
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4I0D
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4I12
 | | Design and synthesis of thiophene dihydroisoquinolins as novel BACE-1 inhibitors | | 分子名称: | 2-{(1S)-1-{[(1Z)-6-chloro-3,3-dimethyl-3,4-dihydroisoquinolin-1(2H)-ylidene]amino}-2-[2-propyl-4-(1H-pyrazol-4-yl)thiophen-3-yl]ethyl}pyrimidin-4(5H)-one, Beta-secretase 1, SODIUM ION, ... | | 著者 | Lougheed, J.C, Brecht, E, Yao, N.H. | | 登録日 | 2012-11-19 | | 公開日 | 2013-03-06 | | 最終更新日 | 2018-01-24 | | 実験手法 | X-RAY DIFFRACTION (1.78 Å) | | 主引用文献 | Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitors.
Bioorg.Med.Chem.Lett., 23, 2013
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4I0G
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4HZT
 | | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates | | 分子名称: | 3-{(1S)-1-[(6-chloro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)amino]-2-phenylethyl}-1,2,4-oxadiazol-5(2H)-one, Beta-secretase 1, ZINC ION | | 著者 | Yao, N, Brecht, E. | | 登録日 | 2012-11-15 | | 公開日 | 2013-03-06 | | 最終更新日 | 2013-04-24 | | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | | 主引用文献 | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates.
Bioorg.Med.Chem.Lett., 23, 2013
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4I1C
 | | Design and synthesis of thiophene dihydroisoquinolins as novel BACE-1 inhibitors | | 分子名称: | BETA-SECRETASE 1, N-(6-chloro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-3-[2-propyl-4-(1H-pyrazol-4-yl)thiophen-3-yl]-L-alanine, ZINC ION | | 著者 | Lougheed, J.C, Brecht, E, Yao, N.H. | | 登録日 | 2012-11-20 | | 公開日 | 2013-03-06 | | 最終更新日 | 2013-07-03 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitors.
Bioorg.Med.Chem.Lett., 23, 2013
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4I6H
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4I5P
 | | Selective & Brain-Permeable Polo-like Kinase-2 (Plk-2) Inhibitors that Reduce -Synuclein Phosphorylation in Rat Brain | | 分子名称: | (7R)-8-cyclopentyl-7-ethyl-5-methyl-2-(1H-pyrrol-2-yl)-7,8-dihydropteridin-6(5H)-one, Serine/threonine-protein kinase PLK2 | | 著者 | Aubele, D.L, Hom, R.K, Adler, M, Galemmo Jr, R.A, Bowers, S, Truong, A.P, Pan, H, Beroza, P. | | 登録日 | 2012-11-28 | | 公開日 | 2013-12-25 | | 最終更新日 | 2024-02-28 | | 実験手法 | X-RAY DIFFRACTION (1.738 Å) | | 主引用文献 | Selective and brain-permeable polo-like kinase-2 (Plk-2) inhibitors that reduce alpha-synuclein phosphorylation in rat brain.
Chemmedchem, 8, 2013
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4I0E
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4I6B
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4I6F
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4I11
 | | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates. | | 分子名称: | Beta-secretase 1, N-(3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-L-phenylalanine, ZINC ION | | 著者 | Bowers, B, Xu, Y, Yuan, S, Probst, G.D, Hom, R.K, Chan, W, Konradi, A.W, Sham, H.L, Zhu, Y.L, Beroza, P, Pan, H, Brecht, E, Yao, N, Lougheed, J, Artis, D.R, Tam, D, Bova, M. | | 登録日 | 2012-11-19 | | 公開日 | 2013-03-06 | | 最終更新日 | 2013-04-24 | | 実験手法 | X-RAY DIFFRACTION (1.89 Å) | | 主引用文献 | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates.
Bioorg.Med.Chem.Lett., 23, 2013
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4I0F
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4I0Z
 | | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates | | 分子名称: | 2-{(1S)-1-[(6-CHLORO-3,3-DIMETHYL-3,4-DIHYDROISOQUINOLIN-1-YL)AMINO]-2-PHENYLETHYL}-4-OXO-1,4-DIHYDROPYRIMIDINE-5-CARBONITRILE, 2-{(1S)-1-[(6-chloro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)amino]-2-phenylethyl}-4-oxo-1,4-dihydropyrimidine-5-carbonitrile, ZINC ION | | 著者 | Lougheed, J.C, Brecht, E, Yao, N.H. | | 登録日 | 2012-11-19 | | 公開日 | 2013-03-06 | | 最終更新日 | 2013-04-24 | | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | | 主引用文献 | Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartates.
Bioorg.Med.Chem.Lett., 23, 2013
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4LNC
 | | Neutron structure of the cyclic glucose bound Xylose Isomerase E186Q mutant | | 分子名称: | MAGNESIUM ION, MANGANESE (II) ION, Xylose isomerase, ... | | 著者 | Munshi, P, Meilleur, F, Myles, D. | | 登録日 | 2013-07-11 | | 公開日 | 2014-02-12 | | 最終更新日 | 2024-02-28 | | 実験手法 | NEUTRON DIFFRACTION (2.19 Å) | | 主引用文献 | Neutron structure of the cyclic glucose-bound xylose isomerase E186Q mutant.
Acta Crystallogr.,Sect.D, 70, 2014
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