8CU7
 
 | Crystal structure of A2AAR-StaR2-bRIL in complex with a novel A2a antagonist, LJ-4517 | 分子名称: | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, (2R,3R,4R)-2-[(8P)-6-amino-2-(hex-1-yn-1-yl)-8-(thiophen-2-yl)-9H-purin-9-yl]oxolane-3,4-diol, Adenosine receptor A2a,Soluble cytochrome b562, ... | 著者 | Shiriaeva, A, Park, D.-J, Kim, G, Lee, Y, Hou, X, Jarhad, D.B, Kim, G, Yu, J, Hyun, Y.E, Kim, W, Gao, Z.-G, Jacobson, K.A, Han, G.W, Stevens, R.C, Jeong, L.S, Choi, S, Cherezov, V. | 登録日 | 2022-05-16 | 公開日 | 2022-08-31 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.05 Å) | 主引用文献 | GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A 2A Adenosine Receptor. J.Med.Chem., 65, 2022
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6DFK
 
 | Crystal structure of the 11S subunit of the Plasmodium falciparum proteasome, PA28 | 分子名称: | SULFATE ION, Subunit of proteaseome activator complex,putative | 著者 | Xie, S.C, Metcalfe, R.D, Gillett, D.L, Tilley, L, Griffin, M.D.W. | 登録日 | 2018-05-15 | 公開日 | 2019-08-07 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (3.1 Å) | 主引用文献 | The structure of the PA28-20S proteasome complex from Plasmodium falciparum and implications for proteostasis. Nat Microbiol, 4, 2019
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6T1B
 
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3IM1
 
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6T0Y
 
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3MDC
 
 | DNA polymerase lambda in complex with dFdCTP | 分子名称: | 2'-deoxy-2',2'-difluorocytidine 5'-(tetrahydrogen triphosphate), DNA (5'-D(*CP*AP*GP*TP*AP*C)-3'), DNA (5'-D(*CP*GP*GP*CP*GP*GP*TP*AP*CP*TP*G)-3'), ... | 著者 | Garcia-Diaz, M, Murray, M, Kunkel, T, Chou, K.M. | 登録日 | 2010-03-30 | 公開日 | 2010-04-28 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (1.999 Å) | 主引用文献 | Interaction between DNA Polymerase lambda and anticancer nucleoside analogs. J.Biol.Chem., 285, 2010
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418D
 
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5AO0
 
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5CSO
 
 | Structure of the complex of type 1 ribosome inactivating protein from Momordica balsamina with a nucleoside, cytidine at 1.78 A resolution | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 4-AMINO-1-BETA-D-RIBOFURANOSYL-2(1H)-PYRIMIDINONE, GLYCEROL, ... | 著者 | Yamin, S, Pandey, S, Kaur, P, Sharma, S, Singh, T.P. | 登録日 | 2015-07-23 | 公開日 | 2015-08-12 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (1.78 Å) | 主引用文献 | Binding and structural studies of the complexes of type 1 ribosome inactivating protein fromMomordica balsaminawith cytosine, cytidine, and cytidine diphosphate. Biochem Biophys Rep, 4, 2015
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1TUM
 
 | MUTT PYROPHOSPHOHYDROLASE-METAL-NUCLEOTIDE-METAL COMPLEX, NMR, 16 STRUCTURES | 分子名称: | COBALT TETRAAMMINE ION, DIPHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER, MAGNESIUM ION, ... | 著者 | Lin, J, Abeygunawardana, C, Frick, D.N, Bessman, M.J, Mildvan, A.S. | 登録日 | 1996-12-05 | 公開日 | 1997-05-15 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of the quaternary MutT-M2+-AMPCPP-M2+ complex and mechanism of its pyrophosphohydrolase action. Biochemistry, 36, 1997
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4DAA
 
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9EIL
 
 | SIRT6 bound to an H3K27Ac nucleosome | 分子名称: | DNA (185-MER), Histone H2A type 1, Histone H2B, ... | 著者 | Markert, J, Wang, Z, Cole, P, Farnung, L. | 登録日 | 2024-11-26 | 公開日 | 2025-07-09 | 実験手法 | ELECTRON MICROSCOPY (3.2 Å) | 主引用文献 | Structural and enzymatic plasticity of SIRT6 deacylase activity. J.Biol.Chem., 301, 2025
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5BJT
 
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1SPG
 
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4L6C
 
 | Crystal structure of human mitochondrial deoxyribonucleotidase in complex with the inhibitor pib-t | 分子名称: | 1,2-ETHANEDIOL, 1-{2-deoxy-3,5-O-[(4-iodophenyl)(phosphono)methylidene]-beta-D-threo-pentofuranosyl}-5-methylpyrimidine-2,4(1H,3H)-dione, 5'(3')-deoxyribonucleotidase, ... | 著者 | Pachl, P, Brynda, J, Rezacova, P. | 登録日 | 2013-06-12 | 公開日 | 2014-09-10 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Conformationally constrained nucleoside phosphonic acids - potent inhibitors of human mitochondrial and cytosolic 5'(3')-nucleotidases. Org.Biomol.Chem., 12, 2014
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2B6A
 
 | Crystal structure of HIV-1 reverse transcriptase (RT) in complex with THR-50 | 分子名称: | 1-(2,6-DIFLUOROBENZYL)-2-(2,6-DIFLUOROPHENYL)-4-METHYL-1H-BENZIMIDAZOLE, Reverse transcriptase p51 subunit, Reverse transcriptase p66 subunit | 著者 | Morningstar, M.L, Roth, T, Smith, M.K, Zajac, M, Watson, K, Buckheit, R.W, Das, K, Zhang, W, Arnold, E, Michejda, C.J. | 登録日 | 2005-09-30 | 公開日 | 2005-11-01 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (2.65 Å) | 主引用文献 | Crystal structure of HIV-1 reverse transcriptase (RT) in complex with THR-50 TO BE PUBLISHED
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6X59
 
 | The mouse cGAS catalytic domain binding to human assembled nucleosome | 分子名称: | Cyclic GMP-AMP synthase, DNA, Histone H2A type 1, ... | 著者 | Pengbiao, X, Pingwei, L, Baoyu, Z. | 登録日 | 2020-05-25 | 公開日 | 2020-09-16 | 最終更新日 | 2025-05-28 | 実験手法 | ELECTRON MICROSCOPY (2.98 Å) | 主引用文献 | The molecular basis of tight nuclear tethering and inactivation of cGAS. Nature, 587, 2020
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8PP7
 
 | human RYBP-PRC1 bound to mononucleosome | 分子名称: | DNA (215-mer), E3 ubiquitin-protein ligase RING2, Histone H2A, ... | 著者 | Ciapponi, M, Benda, C, Mueller, J. | 登録日 | 2023-07-06 | 公開日 | 2024-03-27 | 最終更新日 | 2025-07-09 | 実験手法 | ELECTRON MICROSCOPY (2.91 Å) | 主引用文献 | Structural basis of the histone ubiquitination read-write mechanism of RYBP-PRC1. Nat.Struct.Mol.Biol., 31, 2024
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481D
 
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6XJD
 
 | Two mouse cGAS catalytic domain binding to human assembled nucleosome | 分子名称: | Cyclic GMP-AMP synthase, DNA (145-MER), Histone H2A type 1, ... | 著者 | Xu, P, Li, P, Zhao, B. | 登録日 | 2020-06-23 | 公開日 | 2020-09-16 | 最終更新日 | 2025-05-28 | 実験手法 | ELECTRON MICROSCOPY (6.8 Å) | 主引用文献 | The molecular basis of tight nuclear tethering and inactivation of cGAS. Nature, 587, 2020
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6X5A
 
 | The mouse cGAS catalytic domain binding to human nucleosome that purified from HEK293T cells | 分子名称: | Cyclic GMP-AMP synthase, DNA (natural), Histone H2A type 1, ... | 著者 | Pengbiao, X, Pingwei, L, Baoyu, Z. | 登録日 | 2020-05-25 | 公開日 | 2020-09-16 | 最終更新日 | 2025-05-28 | 実験手法 | ELECTRON MICROSCOPY (4.36 Å) | 主引用文献 | The molecular basis of tight nuclear tethering and inactivation of cGAS. Nature, 587, 2020
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7R1F
 
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7R0E
 
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5AO1
 
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5AO2
 
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