8H8W
| |
8H8V
| |
8H8U
| |
6K1G
| Crystal structure of the L-fucose isomerase soaked with Mn2+ from Raoultella sp. | 分子名称: | L-fucose isomerase, MANGANESE (II) ION | 著者 | Kim, I.J, Kim, D.H, Nam, K.H, Kim, K.H. | 登録日 | 2019-05-10 | 公開日 | 2020-05-13 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.96 Å) | 主引用文献 | Enzymatic synthesis of l-fucose from l-fuculose using a fucose isomerase fromRaoultellasp. and the biochemical and structural analyses of the enzyme. Biotechnol Biofuels, 12, 2019
|
|
6K1F
| Crystal structure of the L-fucose isomerase from Raoultella sp. | 分子名称: | L-fucose isomerase, MANGANESE (II) ION | 著者 | Kim, I.J, Kim, D.H, Nam, K.H, Kim, K.H. | 登録日 | 2019-05-10 | 公開日 | 2020-05-13 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Enzymatic synthesis of l-fucose from l-fuculose using a fucose isomerase fromRaoultellasp. and the biochemical and structural analyses of the enzyme. Biotechnol Biofuels, 12, 2019
|
|
8H2A
| |
8H2B
| Crystal structure of alcohol dehydrogenase from Zobellia galactanivorans | 分子名称: | Alcohol dehydrogenase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, SODIUM ION, ... | 著者 | Brott, S, Bornscheuer, U.T, Nam, K.H. | 登録日 | 2022-10-05 | 公開日 | 2023-10-18 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Unique alcohol dehydrogenases involved in algal sugar utilization by marine bacteria Appl.Microbiol.Biotechnol., 107, 2023
|
|
8D8N
| gRAMP non-match PFS target RNA | 分子名称: | RAMP superfamily protein, RNA (35-MER), RNA (5'-R(P*UP*CP*CP*GP*GP*GP*GP*CP*AP*GP*AP*AP*AP*AP*UP*UP*GP*GP*AP*CP*A)-3'), ... | 著者 | Hu, C, Nam, K.H, Schuler, G, Ke, A. | 登録日 | 2022-06-08 | 公開日 | 2022-08-31 | 最終更新日 | 2024-06-12 | 実験手法 | ELECTRON MICROSCOPY (3.6 Å) | 主引用文献 | Craspase is a CRISPR RNA-guided, RNA-activated protease. Science, 377, 2022
|
|
5HXY
| Crystal structure of XerA recombinase | 分子名称: | PHOSPHATE ION, Tyrosine recombinase XerA | 著者 | Hwang, K.Y, Nam, K.H. | 登録日 | 2016-01-31 | 公開日 | 2017-02-01 | 最終更新日 | 2020-02-19 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Crystal structure of Thermoplasma acidophilum XerA recombinase shows large C-shape clamp conformation and cis-cleavage mode for nucleophilic tyrosine FEBS Lett., 590, 2016
|
|
5HZT
| Crystal structure of Dronpa-Cu2+ | 分子名称: | COPPER (II) ION, Fluorescent protein Dronpa | 著者 | Hwang, K.Y, Nam, K.H. | 登録日 | 2016-02-03 | 公開日 | 2017-03-15 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.84 Å) | 主引用文献 | Crystal structures of Dronpa complexed with quenchable metal ions provide insight into metal biosensor development FEBS Lett., 590, 2016
|
|
5HZU
| Crystal structure of Dronpa-Ni2+ | 分子名称: | Fluorescent protein Dronpa, NICKEL (II) ION | 著者 | Hwang, K.Y, Nam, K.H. | 登録日 | 2016-02-03 | 公開日 | 2017-03-15 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (1.89 Å) | 主引用文献 | Crystal structures of Dronpa complexed with quenchable metal ions provide insight into metal biosensor development FEBS Lett., 590, 2016
|
|
5HZS
| Crystal structure of Dronpa-Co2+ | 分子名称: | COBALT (II) ION, Fluorescent protein Dronpa | 著者 | Hwang, K.Y, Nam, K.H. | 登録日 | 2016-02-03 | 公開日 | 2017-03-15 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.17 Å) | 主引用文献 | Crystal structures of Dronpa complexed with quenchable metal ions provide insight into metal biosensor development FEBS Lett., 590, 2016
|
|
8G9S
| Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications | 分子名称: | AcrIC8, Cas11, Cas5, ... | 著者 | Hu, C, Nam, K.H, Ke, A. | 登録日 | 2023-02-22 | 公開日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3.4 Å) | 主引用文献 | Exploiting activation and inactivation mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Mol.Cell, 84, 2024
|
|
8G9T
| Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications | 分子名称: | AcrIC9, Cas11, Cas5, ... | 著者 | Hu, C, Nam, K.H, Ke, A. | 登録日 | 2023-02-22 | 公開日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3.6 Å) | 主引用文献 | Exploiting activation and inactivation mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Mol.Cell, 84, 2024
|
|
8G9U
| Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications | 分子名称: | CRISPR-associated protein, Csd1 family, Csd2 family, ... | 著者 | Hu, C, Nam, K.H, Ke, A. | 登録日 | 2023-02-22 | 公開日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3 Å) | 主引用文献 | Exploiting activation and inactivation mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Mol.Cell, 84, 2024
|
|
8GAF
| Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications | 分子名称: | Cas11, Cas5, Cas7, ... | 著者 | Hu, C, Nam, K.H, Ke, A. | 登録日 | 2023-02-22 | 公開日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3.64 Å) | 主引用文献 | Exploiting activation and inactivation mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Mol.Cell, 84, 2024
|
|
8GAM
| Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications | 分子名称: | Cas11, Cas5, Cas7, ... | 著者 | Hu, C, Nam, K.H, Ke, A. | 登録日 | 2023-02-23 | 公開日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3.46 Å) | 主引用文献 | Exploiting activation and inactivation mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Mol.Cell, 84, 2024
|
|
8GAN
| Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications | 分子名称: | Cas11, Cas5, Cas7, ... | 著者 | Hu, C, Nam, K.H, Ke, A. | 登録日 | 2023-02-23 | 公開日 | 2024-03-06 | 実験手法 | ELECTRON MICROSCOPY (3.26 Å) | 主引用文献 | Exploiting activation and inactivation mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Mol.Cell, 84, 2024
|
|
4HZ8
| |
4HZ7
| Crystal structure of BglB with glucose | 分子名称: | beta-D-glucopyranose, beta-glucosidase | 著者 | Hwang, K.Y, Nam, K.H. | 登録日 | 2012-11-14 | 公開日 | 2012-12-19 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structural insights into the substrate recognition properties of beta-glucosidase. Biochem.Biophys.Res.Commun., 391, 2010
|
|
4HZ6
| crystal structure of BglB | 分子名称: | Beta-glucosidase, GLYCEROL | 著者 | Hwang, K.Y, Nam, K.H. | 登録日 | 2012-11-14 | 公開日 | 2012-12-19 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Structural insights into the substrate recognition properties of beta-glucosidase. Biochem.Biophys.Res.Commun., 391, 2010
|
|
7TR6
| Cascade complex from type I-A CRISPR-Cas system | 分子名称: | Cas11a, Cas5a, Cas7a, ... | 著者 | Hu, C, Ni, D, Nam, K.H, Majumdar, S, McLean, J, Stahlberg, H, Terns, M, Ke, A. | 登録日 | 2022-01-28 | 公開日 | 2022-08-10 | 最終更新日 | 2022-08-17 | 実験手法 | ELECTRON MICROSCOPY (3.4 Å) | 主引用文献 | Allosteric control of type I-A CRISPR-Cas3 complexes and establishment as effective nucleic acid detection and human genome editing tools. Mol.Cell, 82, 2022
|
|
7TR8
| Cascade complex from type I-A CRISPR-Cas system | 分子名称: | CRISPR-associated endonuclease Cas3-HD, CRISPR-associated helicase Cas3, Cas11a, ... | 著者 | Hu, C, Ni, D, Nam, K.H, Majumdar, S, McLean, J, Stahlberg, H, Terns, M, Ke, A. | 登録日 | 2022-01-28 | 公開日 | 2022-08-10 | 最終更新日 | 2022-08-17 | 実験手法 | ELECTRON MICROSCOPY (3.6 Å) | 主引用文献 | Allosteric control of type I-A CRISPR-Cas3 complexes and establishment as effective nucleic acid detection and human genome editing tools. Mol.Cell, 82, 2022
|
|
7TRA
| Cascade complex from type I-A CRISPR-Cas system | 分子名称: | CRISPR-associated endonuclease Cas3-HD, CRISPR-associated helicase Cas3, Cas11a, ... | 著者 | Hu, C, Ni, D, Nam, K.H, Majumdar, S, McLean, J, Stahlberg, H, Terns, M, Ke, A. | 登録日 | 2022-01-28 | 公開日 | 2022-08-10 | 最終更新日 | 2024-10-09 | 実験手法 | ELECTRON MICROSCOPY (3.3 Å) | 主引用文献 | Allosteric control of type I-A CRISPR-Cas3 complexes and establishment as effective nucleic acid detection and human genome editing tools. Mol.Cell, 82, 2022
|
|
7TR9
| Cascade complex from type I-A CRISPR-Cas system | 分子名称: | CRISPR-associated endonuclease Cas3-HD, CRISPR-associated helicase Cas3, Cas11a, ... | 著者 | Hu, C, Ni, D, Nam, K.H, Majumdar, S, McLean, J, Stahlberg, H, Terns, M, Ke, A. | 登録日 | 2022-01-28 | 公開日 | 2022-08-10 | 最終更新日 | 2024-10-16 | 実験手法 | ELECTRON MICROSCOPY (3.9 Å) | 主引用文献 | Allosteric control of type I-A CRISPR-Cas3 complexes and establishment as effective nucleic acid detection and human genome editing tools. Mol.Cell, 82, 2022
|
|