PDB: 35127 件ウェブページステータス検索Chemie searchBIRD

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1VEA	Crystal Structure of HutP, an RNA binding antitermination protein 分子名称: Hut operon positive regulatory protein, N-(2-NAPHTHYL)HISTIDINAMIDE 著者 Kumarevel, T.S, Fujimoto, Z, Karthe, P, Oda, M, Mizuno, H, Kumar, P.K.R. 登録日 2004-03-29 公開日 2004-07-20 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (2.8 Å) 主引用文献 Crystal Structure of Activated HutP; An RNA Binding Protein that Regulates Transcription of the hut Operon in Bacillus subtilis Structure, 12, 2004
1SNY	Carbonyl reductase Sniffer of D. melanogaster 分子名称: NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, sniffer CG10964-PA 著者 Sgraja, T, Ulschmid, J, Becker, K, Schneuwly, S, Klebe, G, Reuter, K, Heine, A. 登録日 2004-03-12 公開日 2004-09-28 最終更新日 2011-07-13 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Structural Insights into the Neuroprotective-acting Carbonyl Reductase Sniffer of Drosophila melanogaster. J.Mol.Biol., 342, 2004
3DD4	Structural Basis of KChIP4a Modulation of Kv4.3 Slow Inactivation 分子名称: CALCIUM ION, Kv channel-interacting protein 4 著者 Chai, J, Wang, H, Wang, K. 登録日 2008-06-05 公開日 2008-12-23 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (3 Å) 主引用文献 Structural Insights into KChIP4a Modulation of Kv4.3 Inactivation. J.Biol.Chem., 284, 2009
6QIO	Ternary complex of FcRn ectodomain, FcRn binding optimised human serum albumin and the human growth hormone derivative somapacitan 分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, Beta-2-microglobulin, CYSTEINE, ... 著者 Johansson, E. 登録日 2019-01-21 公開日 2020-02-05 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 Identification of Binding Sites on Human Serum Albumin for Somapacitan, a Long-Acting Growth Hormone Derivative. Biochemistry, 59, 2020
5DZO	Crystal structure of human T-cell immunoglobulin and mucin domain protein 1 分子名称: Hepatitis A virus cellular receptor 1, NITRATE ION, SODIUM ION 著者 Yuan, S, Rao, Z, Wang, X. 登録日 2015-09-25 公開日 2015-11-25 最終更新日 2016-02-10 実験手法 X-RAY DIFFRACTION (1.301 Å) 主引用文献 TIM-1 acts a dual-attachment receptor for Ebolavirus by interacting directly with viral GP and the PS on the viral envelope. Protein Cell, 6, 2015
7WZO	Crystal structure of the SARS-CoV-2 nucleocapsid protein N-terminal domain in complex with Ubl1 分子名称: Nucleoprotein, nsp3 著者 Ni, X.C, Zhou, R.J, Lei, J. 登録日 2022-02-18 公開日 2023-02-01 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.64 Å) 主引用文献 Structural insights into ribonucleoprotein dissociation by nucleocapsid protein interacting with non-structural protein 3 in SARS-CoV-2. Commun Biol, 6, 2023
3ZXJ	Engineering the active site of a GH43 glycoside hydrolase generates a biotechnologically significant enzyme that displays both endo- xylanase and exo-arabinofuranosidase activity 分子名称: 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, DI(HYDROXYETHYL)ETHER, HIAXHD3, ... 著者 McKee, L.S, Pena, M.J, Rogowski, A, Jackson, A, Lewis, R.J, York, W.S, Krogh, K.B.R.M, Vikso-Nielsen, A, Skjot, M, Gilbert, H.J, Marles-Wright, J. 登録日 2011-08-11 公開日 2012-04-18 最終更新日 2012-05-02 実験手法 X-RAY DIFFRACTION (1.85 Å) 主引用文献 Introducing Endo-Xylanase Activity Into an Exo-Acting Arabinofuranosidase that Targets Side Chains. Proc.Natl.Acad.Sci.USA, 109, 2012
3ZXK	Engineering the active site of a GH43 glycoside hydrolase generates a biotechnologically significant enzyme that displays both endo- xylanase and exo-arabinofuranosidase activity 分子名称: 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, HIAXHD3, alpha-L-arabinofuranose-(1-2)-[beta-D-xylopyranose-(1-4)]beta-D-xylopyranose-(1-4)-beta-D-xylopyranose 著者 McKee, L.S, Pena, M.J, Rogowski, A, Jackson, A, Lewis, R.J, York, W.S, Krogh, K.B.R.M, Vikso-Nielsen, A, Skjot, M, Gilbert, H.J, Marles-Wright, J. 登録日 2011-08-11 公開日 2012-04-18 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (1.44 Å) 主引用文献 Introducing Endo-Xylanase Activity Into an Exo-Acting Arabinofuranosidase that Targets Side Chains. Proc.Natl.Acad.Sci.USA, 109, 2012
3ZXL	Engineering the active site of a GH43 glycoside hydrolase generates a biotechnologically significant enzyme that displays both endo- xylanase and exo-arabinofuranosidase activity 分子名称: 2-[3-(2-HYDROXY-1,1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, HIAXHD3 著者 McKee, L.S, Pena, M.J, Rogowski, A, Jackson, A, Lewis, R.J, York, W.S, Krogh, K.B.R.M, Vikso-Nielsen, A, Skjot, M, Gilbert, H.J, Marles-Wright, J. 登録日 2011-08-11 公開日 2012-04-18 最終更新日 2023-12-20 実験手法 X-RAY DIFFRACTION (1.871 Å) 主引用文献 Introducing Endo-Xylanase Activity Into an Exo-Acting Arabinofuranosidase that Targets Side Chains. Proc.Natl.Acad.Sci.USA, 109, 2012
7X39	Structure of CIZ1 bound ERH 分子名称: Enhancer of rudimentary homolog,Cip1-interacting zinc finger protein 著者 Wang, X, Xu, C. 登録日 2022-02-28 公開日 2022-08-31 最終更新日 2023-11-29 実験手法 X-RAY DIFFRACTION (2.85 Å) 主引用文献 Molecular basis for the recognition of CIZ1 by ERH. Febs J., 290, 2023
4E3B	Crystal structure of Tax-Interacting Protein-1 (TIP-1) PDZ domain bound to iCAL36-L (ANSRWPTSIL) peptide 分子名称: Tax1-binding protein 3, iCAL50 peptide 著者 Amacher, J.F, Madden, D.R. 登録日 2012-03-09 公開日 2012-12-26 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.5 Å) 主引用文献 Stereochemical Determinants of C-terminal Specificity in PDZ Peptide-binding Domains: A NOVEL CONTRIBUTION OF THE CARBOXYLATE-BINDING LOOP. J.Biol.Chem., 288, 2013
6TT3	Crystal structure of 'Res_S2 mutant human Angiotensin-1 converting enzyme N-domain in complex with SG6. 分子名称: (2~{S})-1-[(2~{S})-2-[[(1~{S})-1-[(2~{S})-1-[(2~{S})-2-azanyl-4-oxidanyl-4-oxidanylidene-butanoyl]pyrrolidin-2-yl]-2-oxidanyl-2-oxidanylidene-ethyl]amino]propanoyl]pyrrolidine-2-carboxylic acid, 1,2-ETHANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... 著者 Cozier, G.E, Acharya, K.R. 登録日 2019-12-23 公開日 2020-04-01 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.7 Å) 主引用文献 ACE-domain selectivity extends beyond direct interacting residues at the active site. Biochem.J., 477, 2020
6QLY	IDOL FERM domain 分子名称: 1,2-ETHANEDIOL, E3 ubiquitin-protein ligase MYLIP, SULFATE ION 著者 Martinelli, L, Sixma, T.K. 登録日 2019-02-01 公開日 2020-02-19 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Structural analysis of the LDL receptor-interacting FERM domain in the E3 ubiquitin ligase IDOL reveals an obscured substrate-binding site. J.Biol.Chem., 295, 2020
6TT1	Crystal structure of 'Res_S2 mutant human Angiotensin-1 converting enzyme N-domain in complex with 33RE. 分子名称: 1,2-ETHANEDIOL, 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 Cozier, G.E, Acharya, K.R. 登録日 2019-12-23 公開日 2020-04-01 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 ACE-domain selectivity extends beyond direct interacting residues at the active site. Biochem.J., 477, 2020
6TT4	Crystal structure of 'Res_S2 mutant human Angiotensin-1 converting enzyme N-domain in complex with omapatrilat. 分子名称: 1,2-ETHANEDIOL, 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 Cozier, G.E, Acharya, K.R. 登録日 2019-12-23 公開日 2020-04-01 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 ACE-domain selectivity extends beyond direct interacting residues at the active site. Biochem.J., 477, 2020
7E83	CryoEM structure of the human Kv4.2-KChIP1 complex, intracellular region 分子名称: Kv channel-interacting protein 1, Potassium voltage-gated channel subfamily D member 2 著者 Kise, Y, Nureki, O. 登録日 2021-02-28 公開日 2021-10-13 最終更新日 2024-06-05 実験手法 ELECTRON MICROSCOPY (3.1 Å) 主引用文献 Structural basis of gating modulation of Kv4 channel complexes. Nature, 599, 2021
7E84	CryoEM structure of human Kv4.2-KChIP1 complex 分子名称: Kv channel-interacting protein 1, Potassium voltage-gated channel subfamily D member 2 著者 Kise, Y, Nureki, O. 登録日 2021-02-28 公開日 2021-10-13 最終更新日 2024-06-05 実験手法 ELECTRON MICROSCOPY (3.1 Å) 主引用文献 Structural basis of gating modulation of Kv4 channel complexes. Nature, 599, 2021
7E8E	CryoEM structure of human Kv4.2-DPP6S-KChIP1 complex, transmembrane and intracellular region 分子名称: Dipeptidyl aminopeptidase-like protein 6, Kv channel-interacting protein 1, Potassium voltage-gated channel subfamily D member 2 著者 Kise, Y, Nureki, O. 登録日 2021-03-01 公開日 2021-10-13 最終更新日 2024-06-05 実験手法 ELECTRON MICROSCOPY (3.9 Å) 主引用文献 Structural basis of gating modulation of Kv4 channel complexes. Nature, 599, 2021
7E8H	CryoEM structure of human Kv4.2-DPP6S-KChIP1 complex 分子名称: Dipeptidyl aminopeptidase-like protein 6, Kv channel-interacting protein 1, Potassium voltage-gated channel subfamily D member 2 著者 Kise, Y, Nureki, O. 登録日 2021-03-01 公開日 2021-10-13 最終更新日 2022-02-16 実験手法 ELECTRON MICROSCOPY (4.5 Å) 主引用文献 Structural basis of gating modulation of Kv4 channel complexes. Nature, 599, 2021
8CIH	Structure of FL CINP 分子名称: Cyclin-dependent kinase 2-interacting protein, SODIUM ION 著者 Foglizzo, M, Zeqiraj, E. 登録日 2023-02-09 公開日 2024-02-21 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 The SPATA5-SPATA5L1 ATPase complex directs replisome proteostasis to ensure genome integrity. Cell, 187, 2024
7F3F	CryoEM structure of human Kv4.2-KChIP1 complex 分子名称: Isoform 2 of Kv channel-interacting protein 1, Potassium voltage-gated channel subfamily D member 2 著者 Kise, Y, Nureki, O. 登録日 2021-06-16 公開日 2021-10-13 最終更新日 2024-06-12 実験手法 ELECTRON MICROSCOPY (3.1 Å) 主引用文献 Structural basis of gating modulation of Kv4 channel complexes. Nature, 599, 2021
6QLZ	IDOL F3ab subdomain 分子名称: E3 ubiquitin-protein ligase MYLIP 著者 Martinelli, L, Johansson, P, Wan, P.T, Gunnarsson, J, Guo, H, Boyd, H. 登録日 2019-02-01 公開日 2020-02-19 最終更新日 2024-01-24 実験手法 X-RAY DIFFRACTION (2.343 Å) 主引用文献 Structural analysis of the LDL receptor-interacting FERM domain in the E3 ubiquitin ligase IDOL reveals an obscured substrate-binding site. J.Biol.Chem., 295, 2020
6HHO	Crystal structure of RIP1 kinase in complex with GSK547 分子名称: 6-[4-[(5~{S})-5-[3,5-bis(fluoranyl)phenyl]pyrazolidin-1-yl]carbonylpiperidin-1-yl]pyrimidine-4-carbonitrile, Receptor-interacting serine/threonine-protein kinase 1 著者 Thorpe, J.H, Harris, P.A. 登録日 2018-08-28 公開日 2018-12-12 最終更新日 2024-01-17 実験手法 X-RAY DIFFRACTION (3.49 Å) 主引用文献 RIP1 Kinase Drives Macrophage-Mediated Adaptive Immune Tolerance in Pancreatic Cancer. Cancer Cell, 34, 2018
2AC5	Structure of human Mnk2 Kinase Domain mutant D228G 分子名称: MAP kinase-interacting serine/threonine kinase 2, ZINC ION 著者 Jauch, R, Wahl, M.C, Jakel, S, Schreiter, K, Aicher, B, Jackle, H. 登録日 2005-07-18 公開日 2005-10-04 最終更新日 2024-05-29 実験手法 X-RAY DIFFRACTION (3.2 Å) 主引用文献 Crystal structures of the Mnk2 kinase domain reveal an inhibitory conformation and a zinc binding site. Structure, 13, 2005
2AC3	Structure of human Mnk2 Kinase Domain 分子名称: MAP kinase-interacting serine/threonine kinase 2, ZINC ION 著者 Jauch, R, Wahl, M.C, Netter, C, Jakel, S, Schreiter, K, Aicher, B, Jackle, H. 登録日 2005-07-18 公開日 2005-10-04 最終更新日 2024-03-13 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Crystal structures of the Mnk2 kinase domain reveal an inhibitory conformation and a zinc binding site. Structure, 13, 2005

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