1STC
 
 | CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH STAUROSPORINE | 分子名称: | CAMP-DEPENDENT PROTEIN KINASE, PROTEIN KINASE INHIBITOR, STAUROSPORINE | 著者 | Prade, L, Engh, R.A, Girod, A, Kinzel, V, Huber, R, Bossemeyer, D. | 登録日 | 1997-10-10 | 公開日 | 1998-02-25 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Staurosporine-induced conformational changes of cAMP-dependent protein kinase catalytic subunit explain inhibitory potential. Structure, 5, 1997
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3VMM
 
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7X91
 
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7X8W
 
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7X92
 
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7X8Z
 
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7X8Y
 
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7X90
 
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2ZU0
 
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5AWG
 
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8W8M
 
 | Cryo-EM structure of helical filament of MyD88 TIR | 分子名称: | Myeloid differentiation primary response protein MyD88 | 著者 | Kasai, K, Imamura, K, Narita, A, Makino, F, Miyata, T, Kato, T, Namba, K, Onishi, H, Tochio, H. | 登録日 | 2023-09-04 | 公開日 | 2024-09-04 | 最終更新日 | 2025-03-26 | 実験手法 | ELECTRON MICROSCOPY (3.28 Å) | 主引用文献 | From Monomers to Oligomers: Structural Mechanism of Receptor-Triggered MyD88 Assembly in Innate Immune Signaling Biorxiv, 2024
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2Z9S
 
 | Crystal Structure Analysis of rat HBP23/Peroxiredoxin I, Cys52Ser mutant | 分子名称: | Peroxiredoxin-1 | 著者 | Matsumura, T, Okamoto, K, Nishino, T, Abe, Y. | 登録日 | 2007-09-25 | 公開日 | 2007-11-20 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Dimer-Oligomer Interconversion of Wild-type and Mutant Rat 2-Cys Peroxiredoxin: DISULFIDE FORMATION AT DIMER-DIMER INTERFACES IS NOT ESSENTIAL FOR DECAMERIZATION J.Biol.Chem., 283, 2008
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5AWF
 
 | Crystal structure of SufB-SufC-SufD complex from Escherichia coli | 分子名称: | FeS cluster assembly protein SufB, FeS cluster assembly protein SufD, Probable ATP-dependent transporter SufC | 著者 | Hirabayashi, K, Wada, K. | 登録日 | 2015-07-03 | 公開日 | 2015-11-11 | 最終更新日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.957 Å) | 主引用文献 | Functional Dynamics Revealed by the Structure of the SufBCD Complex, a Novel ATP-binding Cassette (ABC) Protein That Serves as a Scaffold for Iron-Sulfur Cluster Biogenesis J.Biol.Chem., 290, 2015
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7X93
 
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7X95
 
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7X94
 
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7X96
 
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7XGK
 
 | Human renin in complex with compound1 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Renin, UNKNOWN LIGAND | 著者 | Kashima, A. | 登録日 | 2022-04-05 | 公開日 | 2022-08-31 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Discovery of Novel 2-Carbamoyl Morpholine Derivatives as Highly Potent and Orally Active Direct Renin Inhibitors. Acs Med.Chem.Lett., 13, 2022
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7XGO
 
 | Human renin in complex with compound2 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Renin, UNKNOWN LIGAND | 著者 | Kashima, A. | 登録日 | 2022-04-05 | 公開日 | 2022-08-31 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Discovery of Novel 2-Carbamoyl Morpholine Derivatives as Highly Potent and Orally Active Direct Renin Inhibitors. Acs Med.Chem.Lett., 13, 2022
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7XGP
 
 | Human renin in complex with compound3 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, Renin, UNKNOWN LIGAND | 著者 | Kashima, A. | 登録日 | 2022-04-05 | 公開日 | 2022-09-07 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.65 Å) | 主引用文献 | Discovery of SPH3127: A Novel, Highly Potent, and Orally Active Direct Renin Inhibitor. J.Med.Chem., 65, 2022
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2ZHP
 
 | Crystal structure of bleomycin-binding protein from Streptoalloteichus hindustanus complexed with bleomycin derivative | 分子名称: | Bleomycin resistance protein, CHLORIDE ION, COPPER (II) ION, ... | 著者 | Okumura, H, Miyazaki, I, Simizu, S, Osada, H. | 登録日 | 2008-02-06 | 公開日 | 2009-02-17 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Structure-Affinity Relationship Study of Bleomycins and Shble protein Using a Chemical Array To be Published
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7XES
 
 | NifS with L-penicillamine | 分子名称: | (2~{R})-3-methyl-2-[(~{E})-[2-methyl-3-oxidanyl-5-(phosphonooxymethyl)pyridin-4-yl]methylideneamino]-3-sulfanyl-butanoic acid, CHLORIDE ION, Cysteine desulfurase IscS, ... | 著者 | Nakamura, R, Fujishiro, T. | 登録日 | 2022-03-31 | 公開日 | 2023-04-05 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | X-ray crystallographic snapshots of the thioazolidine formation upon the PLP during inhibition of SufS by D-cysteine to be published
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7XEQ
 
 | NifS with D-cysteine | 分子名称: | (2~{S},4~{S})-2-[2-methyl-3-oxidanyl-5-(phosphonooxymethyl)pyridin-4-yl]-1,3-thiazolidine-4-carboxylic acid, CHLORIDE ION, Cysteine desulfurase IscS, ... | 著者 | Nakamura, R, Fujishiro, T. | 登録日 | 2022-03-31 | 公開日 | 2023-04-05 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | X-ray crystallographic snapshots of the thioazolidine formation upon the PLP during inhibition of SufS by D-cysteine to be published
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7XET
 
 | SufS with beta-cyano-L-alanine | 分子名称: | (2~{E})-3-cyano-2-[[2-methyl-3-oxidanyl-5-(phosphonooxymethyl)pyridin-4-yl]methylimino]propanoic acid, Cysteine desulfurase SufS, DI(HYDROXYETHYL)ETHER, ... | 著者 | Nakamura, R, Fujishiro, T. | 登録日 | 2022-03-31 | 公開日 | 2023-04-05 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Inhibition mechanism of SufS by L-propargylglycine to be published
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7XEP
 
 | SufS with L-propargylglycine | 分子名称: | 1,2-ETHANEDIOL, Cysteine desulfurase SufS, DI(HYDROXYETHYL)ETHER, ... | 著者 | Nakamura, R, Fujishiro, T. | 登録日 | 2022-03-31 | 公開日 | 2023-04-05 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (1.78 Å) | 主引用文献 | Inhibition mechanism of SufS by L-propargylglycine to be published
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