1FJN
 
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1D5Q
 | | SOLUTION STRUCTURE OF A MINI-PROTEIN REPRODUCING THE CORE OF THE CD4 SURFACE INTERACTING WITH THE HIV-1 ENVELOPE GLYCOPROTEIN | | 分子名称: | CHIMERIC MINI-PROTEIN | | 著者 | Vita, C, Drakopoulou, E, Vizzanova, J, Rochette, S, Martin, L, Menez, A, Roumestand, C, Yang, Y.S, Ylisastigui, L, Benjouad, A, Gluckman, J.C. | | 登録日 | 1999-10-11 | | 公開日 | 2000-10-11 | | 最終更新日 | 2022-02-16 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Rational engineering of a miniprotein that reproduces the core of the CD4 site interacting with HIV-1 envelope glycoprotein.
Proc.Natl.Acad.Sci.USA, 96, 1999
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4GZ7
 | | The crystal structure of Apo-dihydropyrimidinase from Tetraodon nigroviridis | | 分子名称: | (CARBAMOYLMETHYL-CARBOXYMETHYL-AMINO)-ACETIC ACID, dihydropyrimidinase | | 著者 | Hsien, Y.C, Chen, M.C, Hsu, C.C, Chan, S.I, Yang, Y.S, Chen, C.J. | | 登録日 | 2012-09-06 | | 公開日 | 2013-09-11 | | 最終更新日 | 2024-03-20 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Lysine Carboxylation: Metal and Structure Requirements for Post-translational Modification
To be Published
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4H00
 | | The crystal structure of mon-Zn dihydropyrimidinase from Tetraodon nigroviridis | | 分子名称: | ZINC ION, dihydropyrimidinase | | 著者 | Hsieh, Y.C, Chen, M.C, Hsu, C.C, Chan, S.I, Yang, Y.S, Chen, C.J. | | 登録日 | 2012-09-06 | | 公開日 | 2013-09-11 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Lysine Carboxylation: Metal and Structural Requirements for Post-translational Modification
To be Published
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4H01
 | | The crystal structure of di-Zn dihydropyrimidinase from Tetraodon nigroviridis | | 分子名称: | ZINC ION, dihydropyrimidinase | | 著者 | Hsieh, Y.C, Chen, M.C, Hsu, C.C, Chan, S.I, Yang, Y.S, Chen, C.J. | | 登録日 | 2012-09-06 | | 公開日 | 2013-09-11 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Lysine Carboxylation: Metal and Structural Requirements for Post-translational Modification
To be Published
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2OSG
 | | Solution Structure and Binding Property of the Domain-swapped Dimer of ZO2PDZ2 | | 分子名称: | Tight junction protein ZO-2 | | 著者 | Wu, J.W, Yang, Y.S, Zhang, J.H, Ji, P, Wu, J.H, Shi, Y.Y. | | 登録日 | 2007-02-05 | | 公開日 | 2007-09-25 | | 最終更新日 | 2022-03-16 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Domain-swapped Dimerization of the Second PDZ Domain of ZO2 May Provide a Structural Basis for the Polymerization of Claudins
J.Biol.Chem., 282, 2007
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4LCR
 | | The crystal structure of di-Zn dihydropyrimidinase in complex with NCBA | | 分子名称: | Chromosome 8 SCAF14545, whole genome shotgun sequence, N-(AMINOCARBONYL)-BETA-ALANINE, ... | | 著者 | Hsieh, Y.C, Chen, M.C, Hsu, C.C, Chan, S.I, Yang, Y.S, Chen, C.J. | | 登録日 | 2013-06-22 | | 公開日 | 2013-09-18 | | 最終更新日 | 2014-02-12 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Crystal structures of vertebrate dihydropyrimidinase and complexes from Tetraodon nigroviridis with lysine carbamylation: metal and structural requirements for post-translational modification and function.
J.Biol.Chem., 288, 2013
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4LCQ
 | | The crystal structure of di-Zn dihydropyrimidinase in complex with NCBI | | 分子名称: | (2S)-3-(carbamoylamino)-2-methylpropanoic acid, ZINC ION, dihydropyrimidinase | | 著者 | Hsieh, Y.C, Chen, M.C, Hsu, C.C, Chan, S.I, Yang, Y.S, Chen, C.J. | | 登録日 | 2013-06-22 | | 公開日 | 2013-09-18 | | 最終更新日 | 2014-02-12 | | 実験手法 | X-RAY DIFFRACTION (1.81 Å) | | 主引用文献 | Crystal structures of vertebrate dihydropyrimidinase and complexes from Tetraodon nigroviridis with lysine carbamylation: metal and structural requirements for post-translational modification and function.
J.Biol.Chem., 288, 2013
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4LCS
 | | The crystal structure of di-Zn dihydropyrimidinase in complex with hydantoin | | 分子名称: | Chromosome 8 SCAF14545, whole genome shotgun sequence, ZINC ION, ... | | 著者 | Hsieh, Y.C, Chen, M.C, Hsu, C.C, Chan, S.I, Yang, Y.S. | | 登録日 | 2013-06-23 | | 公開日 | 2013-09-18 | | 最終更新日 | 2014-02-12 | | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | | 主引用文献 | Crystal structures of vertebrate dihydropyrimidinase and complexes from Tetraodon nigroviridis with lysine carbamylation: metal and structural requirements for post-translational modification and function.
J.Biol.Chem., 288, 2013
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2LCU
 | | NMR structure of BC28.1 | | 分子名称: | Bc28.1 | | 著者 | Roumestand, C, Delbecq, S, Yang, Y. | | 登録日 | 2011-05-09 | | 公開日 | 2012-02-08 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Structural and Functional Characterization of Bc28.1, Major Erythrocyte-binding Protein from Babesia canis Merozoite Surface.
J.Biol.Chem., 287, 2012
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2MCF
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1KOD
 | | RNA APTAMER COMPLEXED WITH CITRULLINE, NMR | | 分子名称: | CITRULLINE, RNA (5'-R(P*AP*CP*GP*GP*UP*UP*AP*GP*GP*UP*CP*GP*CP*U)-3'), RNA (5'-R(P*AP*GP*AP*AP*GP*GP*AP*GP*UP*GP*U)-3') | | 著者 | Yang, Y.S, Kochoyan, M, Burgstaller, P, Westhof, E, Famulok, M. | | 登録日 | 1996-03-28 | | 公開日 | 1996-11-08 | | 最終更新日 | 2023-11-15 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Structural basis of ligand discrimination by two related RNA aptamers resolved by NMR spectroscopy.
Science, 272, 1996
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1KOC
 | | RNA APTAMER COMPLEXED WITH ARGININE, NMR | | 分子名称: | ARGININE, RNA (5'-R(P*AP*CP*AP*GP*GP*UP*AP*GP*GP*UP*CP*GP*CP*U)-3'), RNA (5'-R(P*AP*GP*AP*AP*GP*GP*AP*GP*CP*GP*U)-3') | | 著者 | Yang, Y.S, Kochoyan, M, Burgstaller, P, Westhof, E, Famulok, M. | | 登録日 | 1996-03-28 | | 公開日 | 1996-08-17 | | 最終更新日 | 2022-02-23 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Structural basis of ligand discrimination by two related RNA aptamers resolved by NMR spectroscopy.
Science, 272, 1996
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6WPK
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2QP4
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2QP3
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1QTU
 | | SOLUTION STRUCTURE OF THE ONCOPROTEIN P13MTCP1 | | 分子名称: | PROTEIN (PRODUCT OF THE MTCP1 ONCOGENE) | | 著者 | Guignard, L, Padilla, A, Mispelter, J, Yang, Y.-S, Stern, M.-H, Lhoste, J.-M, Roumestand, C. | | 登録日 | 1999-06-29 | | 公開日 | 2001-01-19 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Backbone dynamics and solution structure refinement of the 15N-labeled human oncogenic protein p13MTCP1: comparison with X-ray data.
J.Biomol.NMR, 17, 2000
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1UXD
 | | Fructose repressor DNA-binding domain, NMR, 34 structures | | 分子名称: | FRUCTOSE REPRESSOR | | 著者 | Penin, F, Geourjon, C, Montserret, R, Bockmann, A, Lesage, A, Yang, Y, Bonod-Bidaud, C, Cortay, J.C, Negre, D, Cozzone, A.J, Deleage, G. | | 登録日 | 1996-12-26 | | 公開日 | 1997-04-01 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Three-dimensional structure of the DNA-binding domain of the fructose repressor from Escherichia coli by 1H and 15N NMR.
J.Mol.Biol., 270, 1997
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1UXC
 | | FRUCTOSE REPRESSOR DNA-BINDING DOMAIN, NMR, MINIMIZED STRUCTURE | | 分子名称: | FRUCTOSE REPRESSOR | | 著者 | Penin, F, Geourjon, C, Montserret, R, Bockmann, A, Lesage, A, Yang, Y, Bonod-Bidaud, C, Cortay, J.C, Negre, D, Cozzone, A.J, Deleage, G. | | 登録日 | 1996-12-26 | | 公開日 | 1997-04-21 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Three-dimensional structure of the DNA-binding domain of the fructose repressor from Escherichia coli by 1H and 15N NMR.
J.Mol.Biol., 270, 1997
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1QTT
 | | SOLUTION STRUCTURE OF THE ONCOPROTEIN P13MTCP1 | | 分子名称: | PRODUCT OF THE MTCP1 ONCOGENE | | 著者 | Guignard, L, Padilla, A, Mispelter, J, Yang, Y.-S, Stern, M.-H, Lhoste, J.-M, Roumestand, C. | | 登録日 | 1999-06-29 | | 公開日 | 2001-01-19 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Backbone dynamics and solution structure refinement of the 15N-labeled human oncogenic protein p13MTCP1: comparison with X-ray data.
J.Biomol.NMR, 17, 2000
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1JSG
 | | CRYSTAL STRUCTURE OF P14TCL1, AN ONCOGENE PRODUCT INVOLVED IN T-CELL PROLYMPHOCYTIC LEUKEMIA, REVEALS A NOVEL B-BARREL TOPOLOGY | | 分子名称: | ONCOGENE PRODUCT P14TCL1 | | 著者 | Hoh, F, Yang, Y.-S, Guignard, L, Padilla, A, Stern, R.-H, Lhoste, J.-M, Van Tilbeurgh, H. | | 登録日 | 1997-12-03 | | 公開日 | 1998-03-18 | | 最終更新日 | 2024-02-07 | | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | | 主引用文献 | Crystal structure of p14TCL1, an oncogene product involved in T-cell prolymphocytic leukemia, reveals a novel beta-barrel topology.
Structure, 6, 1998
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1HP8
 | | SOLUTION STRUCTURE OF HUMAN P8-MTCP1, A CYSTEINE-RICH PROTEIN ENCODED BY THE MTCP1 ONCOGENE,REVEALS A NEW ALPHA-HELICAL ASSEMBLY MOTIF, NMR, MINIMIZED AVERAGE STRUCTURE | | 分子名称: | Cx9C motif-containing protein 4 | | 著者 | Barthe, P, Chiche, L, Strub, M.P, Roumestand, C. | | 登録日 | 1997-08-26 | | 公開日 | 1998-03-04 | | 最終更新日 | 2019-08-21 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Solution structure of human p8MTCP1, a cysteine-rich protein encoded by the MTCP1 oncogene, reveals a new alpha-helical assembly motif.
J.Mol.Biol., 274, 1997
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2JO7
 | | Solution structure of the adhesion protein Bd37 from Babesia divergens | | 分子名称: | Glycosylphosphatidylinositol-anchored merozoite surface protein | | 著者 | Auguin, D, Yang, Y, Lohr, F, Arold, S, Schetters, T, Precigout, E, Gorenflot, A, Delbecq, S, Roumestand, C. | | 登録日 | 2007-02-26 | | 公開日 | 2007-12-11 | | 最終更新日 | 2023-12-20 | | 実験手法 | SOLUTION NMR | | 主引用文献 | The Solution Structure of the Adhesion Protein Bd37 from Babesia divergens Reveals Structural Homology with Eukaryotic Proteins Involved in Membrane Trafficking
J.Mol.Biol., 375, 2007
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8D0I
 | | Human SARM1 bound to an NB-3 eADPR adduct | | 分子名称: | NAD(+) hydrolase SARM1, [[(2~{R},3~{S},4~{R},5~{R})-5-imidazo[2,1-f]purin-3-yl-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(2~{R},3~{S},4~{R},5~{R})-5-[4-[(1~{S})-1-[methyl-[2,2,2-tris(fluoranyl)ethylcarbamoyl]amino]ethyl]pyridin-1-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methyl hydrogen phosphate | | 著者 | Bratkowski, M.A, Mathur, P. | | 登録日 | 2022-05-26 | | 公開日 | 2022-09-21 | | 最終更新日 | 2023-10-25 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Uncompetitive, adduct-forming SARM1 inhibitors are neuroprotective in preclinical models of nerve injury and disease.
Neuron, 110, 2022
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8D0M
 | | Human CD38 ectodomain bound to a 78c-ADPR adduct | | 分子名称: | ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1, [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(2~{R},3~{S},4~{R},5~{R})-5-[5-[4-[[4-(2-methoxyethoxy)cyclohexyl]amino]-1-methyl-2-oxidanylidene-quinolin-6-yl]-1,3-thiazol-3-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methyl hydrogen phosphate | | 著者 | Bratkowski, M.A, Gu, W. | | 登録日 | 2022-05-26 | | 公開日 | 2022-09-21 | | 最終更新日 | 2023-10-25 | | 実験手法 | X-RAY DIFFRACTION (2.04 Å) | | 主引用文献 | Uncompetitive, adduct-forming SARM1 inhibitors are neuroprotective in preclinical models of nerve injury and disease.
Neuron, 110, 2022
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