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PDB: 48 件

2GZR
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Enterobactin and Salmochelin Hydrolase IroE
分子名称: IroE protein
著者Larsen, N.A, Walsh, C.T.
登録日2006-05-11
公開日2006-09-05
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structural Characterization of Enterobactin Hydrolase IroE.
Biochemistry, 45, 2006
2GZS
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Enterobactin Hydolase IroE Complex with DFP
分子名称: DIISOPROPYL PHOSPHONATE, IroE protein
著者Larsen, N.A, Walsh, C.T.
登録日2006-05-12
公開日2006-09-05
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.4 Å)
主引用文献Structural Characterization of Enterobactin Hydrolase IroE.
Biochemistry, 45, 2006
1U4C
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Structure of spindle checkpoint protein Bub3
分子名称: Cell cycle arrest protein BUB3
著者Larsen, N.A, Harrison, S.C.
登録日2004-07-23
公開日2004-08-03
最終更新日2019-08-14
実験手法X-RAY DIFFRACTION (2.35 Å)
主引用文献Crystal structure of the spindle assembly checkpoint protein Bub3
J.Mol.Biol., 344, 2004
6P69
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Crystal structure of FGFR1-Y563C (FGFR4 surrogate) covalently bound to compound 11.
分子名称: 1,2-ETHANEDIOL, Fibroblast growth factor receptor 1, N-{2-[(6-{[(2,6-dichloro-3,5-dimethoxyphenyl)carbamoyl][3-(4-methylpiperazin-1-yl)propyl]amino}pyrimidin-4-yl)amino]phenyl}prop-2-enamide, ...
著者Larsen, N.A.
登録日2019-06-03
公開日2019-06-19
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献To be published
TBD
6OWC
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Mutant estrogen receptor alpha (ERa) Y537S covalently bound to H3B-6545.
分子名称: (2Z)-N,N-dimethyl-4-{[2-({5-[(1Z)-4,4,4-trifluoro-1-(3-fluoro-2H-indazol-5-yl)-2-phenylbut-1-en-1-yl]pyridin-2-yl}oxy)ethyl]amino}but-2-enamide, 1,2-ETHANEDIOL, Estrogen receptor
著者Larsen, N.A.
登録日2019-05-09
公開日2019-06-19
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献Mutant estrogen receptor alpha (ERa) Y537S covalently bound to H3B-6545.
To Be Published
1JU3
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BACTERIAL COCAINE ESTERASE COMPLEX WITH TRANSITION STATE ANALOG
分子名称: PHENYL BORONIC ACID, cocaine esterase
著者Larsen, N.A, Turner, J.M, Stevens, J, Rosser, S.J, Basran, A, Lerner, R.A, Bruce, N.C, Wilson, I.A.
登録日2001-08-23
公開日2001-12-21
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (1.58 Å)
主引用文献Crystal structure of a bacterial cocaine esterase.
Nat.Struct.Biol., 9, 2002
1JU4
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BACTERIAL COCAINE ESTERASE COMPLEX WITH PRODUCT
分子名称: BENZOIC ACID, cocaine esterase
著者Larsen, N.A, Turner, J.M, Stevens, J, Rosser, S.J, Basran, A, Lerner, R.A, Bruce, N.C, Wilson, I.A.
登録日2001-08-23
公開日2001-12-21
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (1.63 Å)
主引用文献Crystal structure of a bacterial cocaine esterase.
Nat.Struct.Biol., 9, 2002
1I7Z
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ANTIBODY GNC92H2 BOUND TO LIGAND
分子名称: CHIMERA OF IG GAMMA-1 CHAIN: HUMAN CONSTANT REGION AND MOUSE VARIABLE REGION, CHIMERA OF IG KAPPA CHAIN: HUMAN CONSTANT REGION AND MOUSE VARIABLE REGION, COCAINE
著者Larsen, N.A, Wilson, I.A.
登録日2001-03-12
公開日2001-08-08
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Crystal structure of a cocaine-binding antibody.
J.Mol.Biol., 311, 2001
1JGV
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STRUCTURAL BASIS FOR DISFAVORED ELIMINATION REACTION IN CATALYTIC ANTIBODY 1D4
分子名称: Antibody Heavy Chain, Antibody Light Chain
著者Larsen, N.A, Heine, A, Crane, L, Cravatt, B.F, Lerner, R.A, Wilson, I.A.
登録日2001-06-26
公開日2001-12-05
最終更新日2018-01-31
実験手法X-RAY DIFFRACTION (1.85 Å)
主引用文献Structural basis for a disfavored elimination reaction in catalytic antibody 1D4.
J.Mol.Biol., 314, 2001
1JGU
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STRUCTURAL BASIS FOR DISFAVORED ELIMINATION REACTION IN CATALYTIC ANTIBODY 1D4
分子名称: (2-AMINO-3-PHENYL-BICYCLO[2.2.1]HEPT-2-YL)-PHENYL-METHANONE, Antibody Heavy Chain, Antibody Light Chain, ...
著者Larsen, N.A, Heine, A, Crane, L, Cravatt, B.F, Lerner, R.A, Wilson, I.A.
登録日2001-06-26
公開日2001-12-05
最終更新日2018-01-31
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Structural basis for a disfavored elimination reaction in catalytic antibody 1D4.
J.Mol.Biol., 314, 2001
5SYB
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Crystal structure of human PHF5A
分子名称: 1,2-ETHANEDIOL, PHD finger-like domain-containing protein 5A, ZINC ION
著者Tsai, J.H.C, Teng, T, Zhu, P, Fekkes, P, Larsen, N.A.
登録日2016-08-10
公開日2016-09-07
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (1.82 Å)
主引用文献Splicing modulators act at the branch point adenosine binding pocket defined by the PHF5A-SF3b complex.
Nat Commun, 8, 2017
5ZYA
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SF3b spliceosomal complex bound to E7107
分子名称: PHD finger-like domain-containing protein 5A, POTASSIUM ION, Splicing factor 3B subunit 1, ...
著者Finci, L.I, Larsen, N.A.
登録日2018-05-23
公開日2018-06-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (3.95 Å)
主引用文献The cryo-EM structure of the SF3b spliceosome complex bound to a splicing modulator reveals a pre-mRNA substrate competitive mechanism of action
Genes Dev., 32, 2018
5ECE
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Tankyrase 1 with Phthalazinone 1
分子名称: 1,2-ETHANEDIOL, 2-[4-[3-[(4-oxidanylidene-3~{H}-phthalazin-1-yl)methyl]phenyl]carbonylpiperazin-1-yl]pyridine-3-carbonitrile, ACETATE ION, ...
著者Kazmirski, S.L, Johannes, J, Read, J.A, Howard, T, Larsen, N.A, Ferguson, A.D.
登録日2015-10-20
公開日2015-11-25
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Discovery of AZ0108, an orally bioavailable phthalazinone PARP inhibitor that blocks centrosome clustering.
Bioorg.Med.Chem.Lett., 25, 2015
4HEJ
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Discovery of Selective and Potent Inhibitors of Gram-positive Bacterial Thymidylate Kinase (TMK): Compund 16
分子名称: 5-methyl-1-[(3S)-1-{3-[3-(trifluoromethyl)phenoxy]benzyl}piperidin-3-yl]pyrimidine-2,4(1H,3H)-dione, Thymidylate kinase
著者Martinez-Botella, G, Breen, J, Duffy, J, Dumas, J, Geng, B, Gowers, I, Green, O, Guler, S, Hentemann, M, Hernandez-Juan, F, Joseph-McCarthy, D, Kawatkar, S, Larsen, N, Lazari, O, Loch, J, Macritchie, J.
登録日2012-10-03
公開日2012-10-24
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Discovery of Selective and Potent Inhibitors of Gram-Positive Bacterial Thymidylate Kinase (TMK).
J.Med.Chem., 55, 2012
5VND
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Crystal structure of FGFR1-Y563C (FGFR4 surrogate) covalently bound to H3B-6527
分子名称: 1,2-ETHANEDIOL, Fibroblast growth factor receptor 1, N-{2-[(6-{[(2,6-dichloro-3,5-dimethoxyphenyl)carbamoyl](methyl)amino}pyrimidin-4-yl)amino]-5-(4-ethylpiperazin-1-yl)phenyl}propanamide, ...
著者Tsai, J.H.C, Reynolds, D, Fekkes, P, Smith, P, Larsen, N.A.
登録日2017-04-30
公開日2017-05-24
最終更新日2023-10-04
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献H3B-6527 Is a Potent and Selective Inhibitor of FGFR4 in FGF19-Driven Hepatocellular Carcinoma.
Cancer Res., 77, 2017
7KIE
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Crystal structure of FGFR2 kinase domain gatekeeper mutant V564F in complex with covalent compound 3
分子名称: CITRATE ANION, Fibroblast growth factor receptor 2, GLYCEROL, ...
著者Ke, J, Wibowo, A.S, Carter, J.J, Larsen, N.A.
登録日2020-10-23
公開日2021-02-10
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.47 Å)
主引用文献Discovery of Aminopyrazole Derivatives as Potent Inhibitors of Wild-Type and Gatekeeper Mutant FGFR2 and 3.
Acs Med.Chem.Lett., 12, 2021
7KIA
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Crystal structure of FGFR2 kinase domain gatekeeper mutant V564F in complex with covalent compound 19
分子名称: 1-[4-(4-{4-(4-methylpiperazin-1-yl)-6-[(3-methyl-1H-pyrazol-5-yl)amino]pyrimidin-2-yl}phenyl)piperidin-1-yl]prop-2-en-1-one, CITRATE ANION, Fibroblast growth factor receptor 2, ...
著者Ke, J, Wibowo, A.S, Carter, J.J, Larsen, N.A.
登録日2020-10-23
公開日2021-02-10
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.22 Å)
主引用文献Discovery of Aminopyrazole Derivatives as Potent Inhibitors of Wild-Type and Gatekeeper Mutant FGFR2 and 3.
Acs Med.Chem.Lett., 12, 2021
5JI0
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PPARgamma-RXRalpha(S427F) heterodimer in complex with SRC-1, rosiglitazone, and 9-cis-retanoic acid
分子名称: (9cis)-retinoic acid, 2,4-THIAZOLIDIINEDIONE, 5-[[4-[2-(METHYL-2-PYRIDINYLAMINO)ETHOXY]PHENYL]METHYL]-(9CL), ...
著者Bloudoff, K, Larsen, N.A.
登録日2016-04-21
公開日2017-04-26
実験手法X-RAY DIFFRACTION (1.98 Å)
主引用文献PPARgamma-RXRalpha(S427F) heterodimer in complex with SRC-1, rosiglitazone, and 9-cis-retanoic acid
To Be Published
2OF3
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TOG domain structure from C.elegans Zyg9
分子名称: ZYG-9
著者Al-Bassam, J, Larsen, N.A, Hyman, A.A, Harrison, S.C.
登録日2007-01-02
公開日2007-03-13
最終更新日2023-12-27
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Crystal structure of a TOG domain: conserved features of XMAP215/Dis1-family TOG domains and implications for tubulin binding.
Structure, 15, 2007
1L7Q
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Ser117Ala Mutant of Bacterial Cocaine Esterase cocE
分子名称: BENZOIC ACID, cocaine esterase
著者Turner, J.M, Larsen, N.A, Basran, A, Barbas III, C.F, Bruce, N.C, Wilson, I.A, Lerner, R.A.
登録日2002-03-16
公開日2003-02-11
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (1.76 Å)
主引用文献Biochemical characterization and structural analysis of a highly proficient cocaine esterase
Biochemistry, 41, 2002
1L7R
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Tyr44Phe Mutant of Bacterial Cocaine Esterase cocE
分子名称: cocaine esterase
著者Turner, J.M, Larsen, N.A, Basran, A, Barbas III, C.F, Bruce, N.C, Wilson, I.A, Lerner, R.A.
登録日2002-03-16
公開日2003-02-11
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (1.64 Å)
主引用文献Biochemical characterization and structural analysis of a highly proficient cocaine esterase.
Biochemistry, 41, 2002
1LZL
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Bacterial Heroin Esterase
分子名称: HEROIN ESTERASE
著者Zhu, X, Larsen, N.A, Basran, A, Bruce, N.C, Wilson, I.A.
登録日2002-06-10
公開日2003-01-28
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.3 Å)
主引用文献OBSERVATION OF AN ARSENIC ADDUCT IN AN ACETYL ESTERASE CRYSTAL STRUCTURE
J.Biol.Chem., 278, 2003
1LZK
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BACTERIAL HEROIN ESTERASE COMPLEX WITH TRANSITION STATE ANALOG DIMETHYLARSENIC ACID
分子名称: CACODYLATE ION, HEROIN ESTERASE
著者Zhu, X, Larsen, N.A, Basran, A, Bruce, N.C, Wilson, I.A.
登録日2002-06-10
公開日2003-01-28
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.45 Å)
主引用文献OBSERVATION OF AN ARSENIC ADDUCT IN AN ACETYL ESTERASE CRYSTAL STRUCTURE
J.Biol.Chem., 278, 2003
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