3KEH
| Crystal Structure of N370S Glucocerebrosidase mutant at pH 7.4 | 分子名称: | 2-acetamido-2-deoxy-alpha-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Wei, R.R, Boucher, S, Pan, C.Q, Edmunds, T. | 登録日 | 2009-10-26 | 公開日 | 2010-10-27 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Crystal Structure of Glucocerebrosidase Containing the N370S mutation: Implication on Chaperon Therapy To be Published
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3KE0
| Crystal structure of N370S Glucocerebrosidase at acidic pH. | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-alpha-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Wei, R.R, Boucher, S, Pan, C.Q, Edmunds, T. | 登録日 | 2009-10-23 | 公開日 | 2010-10-27 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Crystal Structure of Glucocerebrosidase Containing the N370S Mutation, Implications for Chaperon Therapy To be Published
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2FTX
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2IGP
| Crystal Structure of Hec1 CH domain | 分子名称: | BETA-MERCAPTOETHANOL, Retinoblastoma-associated protein HEC | 著者 | Wei, R.R, Harrison, S.C. | 登録日 | 2006-09-22 | 公開日 | 2007-01-02 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | The Ndc80/HEC1 complex is a contact point for kinetochore-microtubule attachment. Nat.Struct.Mol.Biol., 14, 2007
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5WHZ
| PGDM1400-10E8v4 CODV Fab | 分子名称: | Anti-HIV CODV-Fab Heavy chain, Anti-HIV CODV-Fab Light chain | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2017-07-18 | 公開日 | 2017-10-11 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (3.549 Å) | 主引用文献 | Trispecific broadly neutralizing HIV antibodies mediate potent SHIV protection in macaques. Science, 358, 2017
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6O8D
| Anti-CD28xCD3 CODV Fab bound to CD28 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Anti-CD28xCD3 CODV Fab Heavy chain, ... | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2019-03-09 | 公開日 | 2019-11-20 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (3.547 Å) | 主引用文献 | Trispecific antibodies enhance the therapeutic efficacy of tumor-directed T cells through T cell receptor co-stimulation To Be Published
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6O89
| Anti-CD28xCD3 CODV Fab | 分子名称: | Anti-CD28xCD3 CODV-Fab Heavy chain, Anti-CD28xCD3 CODV-Fab Light chain | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2019-03-09 | 公開日 | 2019-11-20 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (2.09 Å) | 主引用文献 | Trispecific antibodies enhance the therapeutic efficacy of tumor-directed T cells through T cell receptor co-stimulation Nat Cancer, 1, 2020
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5I8R
| aSMase with zinc | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, Sphingomyelin phosphodiesterase, ... | 著者 | Zhou, Y.F, Wei, R.R. | 登録日 | 2016-02-19 | 公開日 | 2016-09-07 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (3.646 Å) | 主引用文献 | Human acid sphingomyelinase structures provide insight to molecular basis of Niemann-Pick disease. Nat Commun, 7, 2016
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5I85
| aSMase with zinc and phosphocholine | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, PHOSPHOCHOLINE, ... | 著者 | Zhou, Y.F, Wei, R.R. | 登録日 | 2016-02-18 | 公開日 | 2016-09-07 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Human acid sphingomyelinase structures provide insight to molecular basis of Niemann-Pick disease. Nat Commun, 7, 2016
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5I81
| aSMase with zinc | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, SULFATE ION, ... | 著者 | Zhou, Y.F, Wei, R.R. | 登録日 | 2016-02-18 | 公開日 | 2016-09-07 | 最終更新日 | 2021-03-24 | 実験手法 | X-RAY DIFFRACTION (2.25 Å) | 主引用文献 | Human acid sphingomyelinase structures provide insight to molecular basis of Niemann-Pick disease. Nat Commun, 7, 2016
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6AMM
| CAT192 Fab Insertion Mutant H0/L1 | 分子名称: | CAT192 Fab Heavy chain, CAT192 Fab Light chain | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2017-08-10 | 公開日 | 2018-01-31 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Structure-based engineering to restore high affinity binding of an isoform-selective anti-TGF beta 1 antibody. MAbs, 10, 2018
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6AMJ
| CAT192 Fab Wild Type | 分子名称: | CAT192 Fab heavy chain, CAT192 Fab light chain, DI(HYDROXYETHYL)ETHER, ... | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2017-08-09 | 公開日 | 2018-01-31 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.49 Å) | 主引用文献 | Structure-based engineering to restore high affinity binding of an isoform-selective anti-TGF beta 1 antibody. MAbs, 10, 2018
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6AO0
| CAT192 Fab Insertion Mutant H2/L2 | 分子名称: | CAT192 Fab Heavy chain, CAT192 Fab Light chain, SULFATE ION | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2017-08-15 | 公開日 | 2018-01-31 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | Structure-based engineering to restore high affinity binding of an isoform-selective anti-TGF beta 1 antibody. MAbs, 10, 2018
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6ANP
| CAT192 Fab Insertion Mutant H5/L0 | 分子名称: | CAT192 Fab Heavy chain, CAT192 Fab Light chain | 著者 | Lord, D.M, Wei, R.R. | 登録日 | 2017-08-14 | 公開日 | 2018-01-31 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.45 Å) | 主引用文献 | Structure-based engineering to restore high affinity binding of an isoform-selective anti-TGF beta 1 antibody. MAbs, 10, 2018
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3R02
| The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors | 分子名称: | 7-[(cis-4-aminocyclohexyl)amino]-5-bromo-1-benzofuran-2-carboxylic acid, IMIDAZOLE, Proto-oncogene serine/threonine-protein kinase pim-1 | 著者 | Xiang, Y, Hirth, B, Asmussen, G, Biemann, H.-P, Good, A, Fitzgerald, M, Gladysheva, T, Jancsics, K, Liu, J, Metz, M, Papoulis, A, Skerlj, R, Stepp, D.J, Wei, R.R. | 登録日 | 2011-03-07 | 公開日 | 2011-05-11 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors. Bioorg.Med.Chem.Lett., 21, 2011
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3R04
| The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors | 分子名称: | 5-{6-[(trans-4-aminocyclohexyl)amino]pyrazin-2-yl}-1-benzofuran-2-carboxylic acid, IMIDAZOLE, Proto-oncogene serine/threonine-protein kinase pim-1 | 著者 | Xiang, Y, Hirth, B, Asmussen, G, Biemann, H.-P, Good, A, Fitzgerald, M, Gladysheva, T, Jancsics, K, Liu, J, Metz, M, Papoulis, A, Skerlj, R, Stepp, D.J, Wei, R.R. | 登録日 | 2011-03-07 | 公開日 | 2011-05-11 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors. Bioorg.Med.Chem.Lett., 21, 2011
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