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PDB: 12 件
8GY5
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BU of 8gy5 by Molmil
High-resolution structure of the cemiplimab Fab in complex with PD-1
分子名称: Programmed cell death protein 1, heavy chain, light chain
著者Heo, Y.-S, Jeong, T.J.
登録日2022-09-21
公開日2023-10-04
実験手法X-RAY DIFFRACTION (1.98 Å)
主引用文献High-resolution structure of the cemiplimab Fab in complex with PD-1
To Be Published
5Y9J
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BU of 5y9j by Molmil
BAFF in complex with belimumab
分子名称: Tumor necrosis factor ligand superfamily member 13B, belibumab light chain, belimumab heavy chain
著者Heo, Y.-S, Shin, W.
登録日2017-08-25
公開日2018-02-21
最終更新日2019-09-04
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献BAFF-neutralizing interaction of belimumab related to its therapeutic efficacy for treating systemic lupus erythematosus.
Nat Commun, 9, 2018
5Y9K
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Structure of the belimumab Fab fragment
分子名称: belimumab heavy chain, belimumab light chain
著者Heo, Y.-S, Shin, W.
登録日2017-08-25
公開日2018-02-21
最終更新日2024-10-23
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献BAFF-neutralizing interaction of belimumab related to its therapeutic efficacy for treating systemic lupus erythematosus.
Nat Commun, 9, 2018
1UKH
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BU of 1ukh by Molmil
Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
分子名称: 11-mer peptide from C-jun-amino-terminal kinase interacting protein 1, Mitogen-activated protein kinase 8 isoform 4
著者Heo, Y.-S, Kim, Y.K, Sung, B.-J, Lee, H.S, Lee, J.I, Seo, C.I, Park, S.-Y, Kim, J.H, Hyun, Y.-L, Jeon, Y.H, Ro, S, Lee, T.G, Cho, J.M, Hwang, K.Y, Yang, C.-H.
登録日2003-08-23
公開日2004-08-30
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.35 Å)
主引用文献Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
Embo J., 23, 2004
1UKI
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BU of 1uki by Molmil
Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
分子名称: 11-mer peptide from C-jun-amino-terminal kinase interacting protein 1, 2,6-DIHYDROANTHRA/1,9-CD/PYRAZOL-6-ONE, mitogen-activated protein kinase 8 isoform 4
著者Heo, Y.-S, Kim, Y.K, Sung, B.-J, Lee, H.S, Lee, J.I, Seo, C.I, Park, S.-Y, Kim, J.H, Hyun, Y.-L, Jeon, Y.H, Ro, S, Lee, T.G, Cho, J.M, Hwang, K.Y, Yang, C.-H.
登録日2003-08-23
公開日2004-08-30
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
Embo J., 23, 2004
3LPS
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BU of 3lps by Molmil
Crystal structure of parE
分子名称: NOVOBIOCIN, Topoisomerase IV subunit B
著者Jung, H.Y, Heo, Y.-S.
登録日2010-02-05
公開日2011-02-16
最終更新日2024-03-20
実験手法X-RAY DIFFRACTION (2.29 Å)
主引用文献Crystal structure of parE
To be Published
3LNU
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BU of 3lnu by Molmil
Crystal structure of ParE subunit
分子名称: Topoisomerase IV subunit B
著者Jung, H.Y, Heo, Y.-S.
登録日2010-02-03
公開日2011-02-16
最終更新日2024-03-20
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Crystal structure of ParE subunit
To be Published
1UDT
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BU of 1udt by Molmil
Crystal structure of Human Phosphodiesterase 5 complexed with Sildenafil(Viagra)
分子名称: 5-{2-ETHOXY-5-[(4-METHYLPIPERAZIN-1-YL)SULFONYL]PHENYL}-1-METHYL-3-PROPYL-1H,6H,7H-PYRAZOLO[4,3-D]PYRIMIDIN-7-ONE, MAGNESIUM ION, ZINC ION, ...
著者Sung, B.-J, Lee, J.I, Heo, Y.-S, Kim, J.H, Moon, J, Yoon, J.M, Hyun, Y.-L, Kim, E, Eum, S.J, Lee, T.G, Cho, J.M, Park, S.-Y, Lee, J.-O, Jeon, Y.H, Hwang, K.Y, Ro, S.
登録日2003-05-06
公開日2004-05-11
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules
Nature, 425, 2003
1UHO
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Crystal structure of Human Phosphodiesterase 5 complexed with Vardenafil(Levitra)
分子名称: 2-{2-ETHOXY-5-[(4-ETHYLPIPERAZIN-1-YL)SULFONYL]PHENYL}-5-METHYL-7-PROPYLIMIDAZO[5,1-F][1,2,4]TRIAZIN-4(1H)-ONE, MAGNESIUM ION, ZINC ION, ...
著者Sung, B.-J, Lee, J.I, Heo, Y.-S, Kim, J.H, Moon, J, Yoon, J.M, Hyun, Y.-L, Kim, E, Eum, S.J, Lee, T.G, Cho, J.M, Park, S.-Y, Lee, J.-O, Jeon, Y.H, Hwang, K.Y, Ro, S.
登録日2003-07-09
公開日2004-07-09
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules
Nature, 425, 2003
7EOW
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BU of 7eow by Molmil
High-resolution structure of vWF A1 domain in complex with caplacizumab, the first nanobody-based medicine
分子名称: caplacizumab, von Willebrand factor
著者Lee, H.T, Heo, Y.-S.
登録日2021-04-23
公開日2021-07-07
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献High-resolution structure of the vWF A1 domain in complex with caplacizumab, the first nanobody-based medicine for treating acquired TTP.
Biochem.Biophys.Res.Commun., 567, 2021
1UDU
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Crystal structure of Human Phosphodiesterase 5 complexed with tadalafil(Cialis)
分子名称: 6-BENZO[1,3]DIOXOL-5-YL-2-METHYL-2,3,6,7,12,12A-HEXAHYDRO-PYRAZINO[1',2':1,6]PYRIDO[3,4-B]INDOLE-1,4-DIONE, MAGNESIUM ION, ZINC ION, ...
著者Sung, B.-J, Lee, J.I, Heo, Y.-S, Kim, J.H, Moon, J, Yoon, J.M, Hyun, Y.-L, Kim, E, Eum, S.J, Lee, T.G, Cho, J.M, Park, S.-Y, Lee, J.-O, Jeon, Y.H, Hwang, K.Y, Ro, S.
登録日2003-05-06
公開日2004-05-11
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (2.83 Å)
主引用文献Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules
Nature, 425, 2003
7CMP
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BU of 7cmp by Molmil
parE in complex with AMPPNP
分子名称: DNA topoisomerase 4 subunit B, MAGNESIUM ION, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER
著者Jung, H.Y, Heo, Y.-S.
登録日2020-07-28
公開日2021-08-04
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (2.886 Å)
主引用文献Crystal structure of parE in complex with AMPPNP
To Be Published

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件を2024-10-30に公開中

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