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PDB: 84 件
1NDD
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BU of 1ndd by Molmil
STRUCTURE OF NEDD8
分子名称: CHLORIDE ION, PROTEIN (UBIQUITIN-LIKE PROTEIN NEDD8), SULFATE ION
著者Whitby, F.G, Xia, G, Pickart, C.M, Hill, C.P.
登録日1998-08-21
公開日1999-02-23
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Crystal structure of the human ubiquitin-like protein NEDD8 and interactions with ubiquitin pathway enzymes.
J.Biol.Chem., 273, 1998
1FNT
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BU of 1fnt by Molmil
CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION
分子名称: MAGNESIUM ION, PROTEASOME ACTIVATOR PROTEIN PA26, PROTEASOME COMPONENT C1, ...
著者Whitby, F.G, Masters, E, Kramer, L, Knowlton, J.R, Yao, Y, Wang, C.C, Hill, C.P.
登録日2000-08-23
公開日2001-04-11
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (3.2 Å)
主引用文献Structural basis for the activation of 20S proteasomes by 11S regulators.
Nature, 408, 2000
1C1G
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BU of 1c1g by Molmil
CRYSTAL STRUCTURE OF TROPOMYOSIN AT 7 ANGSTROMS RESOLUTION IN THE SPERMINE-INDUCED CRYSTAL FORM
分子名称: TROPOMYOSIN
著者Whitby, F.G, Phillips Jr, G.N.
登録日1999-07-22
公開日2000-02-11
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (7 Å)
主引用文献Crystal structure of tropomyosin at 7 Angstroms resolution.
Proteins, 38, 2000
7S49
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BU of 7s49 by Molmil
Crystal Structure of Inhibitor-bound Galactokinase
分子名称: (4R)-2-[(1,3-benzoxazol-2-yl)amino]-4-(4-chloro-1H-pyrazol-5-yl)-4,6,7,8-tetrahydroquinazolin-5(1H)-one, Galactokinase, PHOSPHATE ION, ...
著者Whitby, F.G.
登録日2021-09-08
公開日2021-09-29
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structure-Based Optimization of Small Molecule Human Galactokinase Inhibitors.
J.Med.Chem., 64, 2021
7S4C
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BU of 7s4c by Molmil
Crystal Structure of Inhibitor-bound Galactokinase
分子名称: 2-({(4R)-4-(2-chlorophenyl)-2-[(6-fluoro-1,3-benzoxazol-2-yl)amino]-6-methyl-1,4-dihydropyrimidine-5-carbonyl}amino)pyridine-4-carboxylic acid, Galactokinase, PHOSPHATE ION, ...
著者Whitby, F.G.
登録日2021-09-08
公開日2021-09-29
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Structure-Based Optimization of Small Molecule Human Galactokinase Inhibitors.
J.Med.Chem., 64, 2021
8V14
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BU of 8v14 by Molmil
Structure of NRAP-1 and its role in NMDAR signaling
分子名称: CALCIUM ION, NMDA receptor auxiliary protein
著者Whitby, F.G, Goodell, D.J, Maricq, A.V, Hill, C.P.
登録日2023-11-19
公開日2024-01-31
最終更新日2024-08-21
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Mechanistic and structural studies reveal NRAP-1-dependent coincident activation of NMDARs.
Cell Rep, 43, 2024
7RCL
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BU of 7rcl by Molmil
Crystal Structure of ADP-bound Galactokinase
分子名称: ADENOSINE-5'-DIPHOSPHATE, Galactokinase, MAGNESIUM ION, ...
著者Whitby, F.G, Hall, M.D.
登録日2021-07-07
公開日2021-09-29
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structure-Based Optimization of Small Molecule Human Galactokinase Inhibitors.
J.Med.Chem., 64, 2021
7RCM
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BU of 7rcm by Molmil
Crystal Structure of ADP-bound Galactokinase
分子名称: ADENOSINE-5'-DIPHOSPHATE, GLYCEROL, Galactokinase, ...
著者Whitby, F.G.
登録日2021-07-07
公開日2021-09-29
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Structure-Based Optimization of Small Molecule Human Galactokinase Inhibitors.
J.Med.Chem., 64, 2021
1AK5
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BU of 1ak5 by Molmil
INOSINE MONOPHOSPHATE DEHYDROGENASE (IMPDH) FROM TRITRICHOMONAS FOETUS
分子名称: INOSINE-5'-MONOPHOSPHATE DEHYDROGENASE, SULFATE ION
著者Whitby, F.G.
登録日1997-05-28
公開日1997-09-17
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Crystal structure of Tritrichomonas foetus inosine-5'-monophosphate dehydrogenase and the enzyme-product complex.
Biochemistry, 36, 1997
5ILS
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BU of 5ils by Molmil
Autoinhibited ETV1
分子名称: ETS translocation variant 1
著者Whitby, F.G, Currie, S.L.
登録日2016-03-04
公開日2017-02-22
最終更新日2019-12-25
実験手法X-RAY DIFFRACTION (1.399 Å)
主引用文献Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5.
Nucleic Acids Res., 45, 2017
5ILV
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BU of 5ilv by Molmil
Uninhibited ETV5
分子名称: ETS translocation variant 5
著者Whitby, F.G, Currie, S.L.
登録日2016-03-04
公開日2017-02-22
最終更新日2019-12-25
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5.
Nucleic Acids Res., 45, 2017
5ILU
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BU of 5ilu by Molmil
Autoinhibited ETV4
分子名称: ETS translocation variant 4
著者Whitby, F.G, Currie, S.L.
登録日2016-03-04
公開日2017-02-22
最終更新日2019-12-25
実験手法X-RAY DIFFRACTION (1.101 Å)
主引用文献Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5.
Nucleic Acids Res., 45, 2017
1LC3
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BU of 1lc3 by Molmil
Crystal Structure of a Biliverdin Reductase Enzyme-Cofactor Complex
分子名称: Biliverdin Reductase A, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, PHOSPHATE ION
著者Whitby, F.G, Phillips, J.D, Hill, C.P, McCoubrey, W, Maines, M.D.
登録日2002-04-05
公開日2002-07-17
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.5 Å)
主引用文献Crystal structure of a biliverdin IXalpha reductase enzyme-cofactor complex.
J.Mol.Biol., 319, 2002
1LC0
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BU of 1lc0 by Molmil
Structure of Biliverdin Reductase and the Enzyme-NADH Complex
分子名称: Biliverdin Reductase A, PHOSPHATE ION
著者Whitby, F.G, Phillips, J.D, Hill, C.P, McCoubrey, W, Maines, M.D.
登録日2002-04-04
公開日2002-07-17
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.2 Å)
主引用文献Crystal structure of a biliverdin IXalpha reductase enzyme-cofactor complex.
J.Mol.Biol., 319, 2002
1URO
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BU of 1uro by Molmil
UROPORPHYRINOGEN DECARBOXYLASE
分子名称: BETA-MERCAPTOETHANOL, PROTEIN (UROPORPHYRINOGEN DECARBOXYLASE)
著者Whitby, F.G, Phillips, J.D, Kushner, J.P, Hill, C.P.
登録日1998-08-21
公開日1998-08-26
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Crystal structure of human uroporphyrinogen decarboxylase.
EMBO J., 17, 1998
4V7O
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BU of 4v7o by Molmil
Proteasome Activator Complex
分子名称: Proteasome activator BLM10, Proteasome component C1, Proteasome component C11, ...
著者Hill, C.P, Whitby, F.G.
登録日2009-12-22
公開日2014-07-09
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (3.005 Å)
主引用文献Structure of a Blm10 complex reveals common mechanisms for proteasome binding and gate opening.
Mol.Cell, 37, 2010
6PSA
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BU of 6psa by Molmil
PIE12 D-PEPTIDE AGAINST HIV ENTRY (IN COMPLEX WITH IQN17 Q577R RESISTANCE MUTANT)
分子名称: CHLORIDE ION, IQN17, PIE12 D-peptide
著者Hill, C.P, Whitby, F.G, Kay, M, Weinstock, M.
登録日2019-07-12
公開日2020-02-05
実験手法X-RAY DIFFRACTION (1.3 Å)
主引用文献Characterization of resistance to a potent D-peptide HIV entry inhibitor.
Retrovirology, 16, 2019
2HTH
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BU of 2hth by Molmil
Structural basis for ubiquitin recognition by the human EAP45/ESCRT-II GLUE domain
分子名称: Ubiquitin, Vacuolar protein sorting protein 36
著者Alam, S.L, Whitby, F.G, Hill, C.P, Sundquist, W.I.
登録日2006-07-25
公開日2006-10-24
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Structural basis for ubiquitin recognition by the human ESCRT-II EAP45 GLUE domain.
Nat.Struct.Mol.Biol., 13, 2006
4R0R
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BU of 4r0r by Molmil
Ebolavirus GP Prehairpin Intermediate Mimic
分子名称: eboIZN21
著者Clinton, T.R, Weinstock, M.T, Jacobsen, M.T, Szabo-Fresnais, N, Pandya, M.J, Whitby, F.G, Herbert, A.S, Prugar, L.I, McKinnon, R, Hill, C.P, Welch, B.D, Dye, J.M, Eckert, D.M, Kay, M.S.
登録日2014-08-01
公開日2014-10-22
最終更新日2024-04-03
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献Design and characterization of ebolavirus GP prehairpin intermediate mimics as drug targets.
Protein Sci., 24, 2015
3C3R
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BU of 3c3r by Molmil
ALIX BRO1 CHMP4C complex
分子名称: Charged multivesicular body protein 4c peptide, GLYCEROL, Programmed cell death 6-interacting protein
著者McCullough, J.B, Fisher, R.D, Whitby, F.G, Sundquist, W.I, Hill, C.P.
登録日2008-01-28
公開日2008-06-10
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.02 Å)
主引用文献ALIX-CHMP4 interactions in the human ESCRT pathway.
Proc.Natl.Acad.Sci.Usa, 105, 2008
3C3O
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BU of 3c3o by Molmil
ALIX Bro1-domain:CHMIP4A co-crystal structure
分子名称: Charged multivesicular body protein 4a peptide, GLYCEROL, Programmed cell death 6-interacting protein
著者McCullough, J.B, Fisher, R.D, Whitby, F.G, Sundquist, W.I, Hill, C.P.
登録日2008-01-28
公開日2008-06-10
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献ALIX-CHMP4 interactions in the human ESCRT pathway.
Proc.Natl.Acad.Sci.Usa, 105, 2008
3L35
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BU of 3l35 by Molmil
PIE12 D-peptide against HIV entry
分子名称: GP41 N-PEPTIDE, HIV ENTRY INHIBITOR PIE12
著者Welch, B.D, Redman, J.S, Paul, S, Whitby, F.G, Weinstock, M.T, Reeves, J.D, Lie, Y.S, Eckert, D.M, Hill, C.P, Root, M.J, Kay, M.S.
登録日2009-12-16
公開日2010-11-03
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.55 Å)
主引用文献Design of a potent D-peptide HIV-1 entry inhibitor with a strong barrier to resistance.
J.Virol., 84, 2010
3L36
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PIE12 D-peptide against HIV entry
分子名称: 3-CYCLOHEXYL-1-PROPYLSULFONIC ACID, GP41 N-PEPTIDE, HIV ENTRY INHIBITOR PIE12
著者Welch, B.D, Redman, J.S, Paul, S, Whitby, F.G, Weinstock, M.T, Reeves, J.D, Lie, Y.S, Eckert, D.M, Hill, C.P, Root, M.J, Kay, M.S.
登録日2009-12-16
公開日2010-11-03
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (1.45 Å)
主引用文献Design of a potent D-peptide HIV-1 entry inhibitor with a strong barrier to resistance.
J.Virol., 84, 2010
8UC6
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BU of 8uc6 by Molmil
Calpain-7:IST1 Complex
分子名称: Calpain-7, IST1 homolog
著者Paine, E, Whitby, F.G, Hill, C.P, Sunquist, W.I.
登録日2023-09-25
公開日2023-10-25
最終更新日2024-05-15
実験手法X-RAY DIFFRACTION (2.701 Å)
主引用文献The Calpain-7 protease functions together with the ESCRT-III protein IST1 within the midbody to regulate the timing and completion of abscission.
Elife, 12, 2023
7JX4
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BU of 7jx4 by Molmil
Crystal Structure of N-Lysine Peptoid-modified Collagen Triple Helix
分子名称: Collagen mimetic peptide with N-Lysine guest
著者Yu, M.S, Whitby, F.G, Hill, C.P, Kessler, J.L, Yang, L.D.
登録日2020-08-26
公開日2021-07-21
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (0.95 Å)
主引用文献Peptoid Residues Make Diverse, Hyperstable Collagen Triple-Helices.
J.Am.Chem.Soc., 143, 2021

 

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