2KDK
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5ILS
| 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
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5ILV
| 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
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5ILU
| 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
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1RN1
| THREE-DIMENSIONAL STRUCTURE OF GLN 25-RIBONUCLEASE T1 AT 1.84 ANGSTROMS RESOLUTION: STRUCTURAL VARIATIONS AT THE BASE RECOGNITION AND CATALYTIC SITES | 分子名称: | RIBONUCLEASE T1 ISOZYME, SULFATE ION | 著者 | Arni, R.K, Pal, G.P, Ravichandran, K.G, Tulinsky, A, Walz Junior, F.G, Metcalf, P. | 登録日 | 1991-11-22 | 公開日 | 1994-01-31 | 最終更新日 | 2019-08-14 | 実験手法 | X-RAY DIFFRACTION (1.84 Å) | 主引用文献 | Three-dimensional structure of Gln25-ribonuclease T1 at 1.84-A resolution: structural variations at the base recognition and catalytic sites. Biochemistry, 31, 1992
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5KZE
| N-acetylneuraminate lyase from methicillin-resistant Staphylococcus aureus | 分子名称: | GLYCEROL, N-acetylneuraminate lyase, SULFATE ION | 著者 | North, R.A, Watson, A.J.A, Pearce, F.G, Muscroft-Taylor, A.C, Friemann, R, Fairbanks, A.J, Dobson, R.C.J. | 登録日 | 2016-07-25 | 公開日 | 2017-01-11 | 最終更新日 | 2023-10-04 | 実験手法 | X-RAY DIFFRACTION (1.74 Å) | 主引用文献 | Structure and inhibition of N-acetylneuraminate lyase from methicillin-resistant Staphylococcus aureus. FEBS Lett., 590, 2016
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5KKE
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3L37
| 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 (1.45 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
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3MGN
| D-Peptide inhibitor PIE71 in complex with IQN17 | 分子名称: | D-PEPTIDE INHIBITOR PIE71, IQN17 | 著者 | Hill, C.P, Whitby, F.G, Kay, M, Francis, N. | 登録日 | 2010-04-07 | 公開日 | 2011-03-02 | 最終更新日 | 2017-11-08 | 実験手法 | X-RAY DIFFRACTION (1.4 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
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3JTL
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3L35
| 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
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3KNX
| HCV NS3 protease domain with P1-P3 macrocyclic ketoamide inhibitor | 分子名称: | (2R)-2-{(3S,13S,16aS,17aR,17bS)-13-[({(1S)-1-[(4,4-dimethyl-2,6-dioxopiperidin-1-yl)methyl]-2,2-dimethylpropyl}carbamoyl)amino]-17,17-dimethyl-1,14-dioxooctadecahydro-2H-cyclopropa[3,4]pyrrolo[1,2-a][1,4]diazacyclohexadecin-3-yl}-2-hydroxy-N-prop-2-en-1-ylethanamide, BETA-MERCAPTOETHANOL, HCV NS3 Protease, ... | 著者 | Venkatraman, S, Velazquez, F, Wu, W, Blackman, M, Chen, K.X, Bogen, S, Nair, L, Tong, X, Chase, R, Hart, A, Agrawal, S, Pichardo, J, Prongay, A, Cheng, K.-C, Girijavallabhan, V, Piwinski, J, Shih, N.-Y, Njoroge, F.G. | 登録日 | 2009-11-12 | 公開日 | 2010-10-27 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.65 Å) | 主引用文献 | Discovery and structure-activity relationship of P1-P3 ketoamide derived macrocyclic inhibitors of hepatitis C virus NS3 protease. J.Med.Chem., 52, 2009
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3L36
| 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
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8V14
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1YA7
| Implications for interactions of proteasome with PAN and PA700 from the 1.9 A structure of a proteasome-11S activator complex | 分子名称: | GLYCEROL, Proteasome alpha subunit, Proteasome beta subunit, ... | 著者 | Forster, A, Masters, E.I, Whitby, F.G, Robinson, H, Hill, C.P. | 登録日 | 2004-12-17 | 公開日 | 2005-07-26 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | The 1.9 A structure of a proteasome-11S activator complex and implications for proteasome-PAN/PA700 interactions. Mol.Cell, 18, 2005
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1URO
| 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
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1YPU
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1YPO
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1YPQ
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1YAU
| Structure of Archeabacterial 20S proteasome- PA26 complex | 分子名称: | GLYCEROL, Proteasome alpha subunit, Proteasome beta subunit, ... | 著者 | Forster, A, Masters, E.I, Whitby, F.G, Robinson, H, Hill, C.P. | 登録日 | 2004-12-17 | 公開日 | 2005-07-26 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | The 1.9 A structure of a proteasome-11S activator complex and implications for proteasome-PAN/PA700 interactions. Mol.Cell, 18, 2005
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1YAR
| Structure of Archeabacterial 20S proteasome mutant D9S- PA26 complex | 分子名称: | GLYCEROL, Proteasome alpha subunit, Proteasome beta subunit, ... | 著者 | Forster, A, Masters, E.I, Whitby, F.G, Robinson, H, Hill, C.P. | 登録日 | 2004-12-17 | 公開日 | 2005-07-26 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | The 1.9 A structure of a proteasome-11S activator complex and implications for proteasome-PAN/PA700 interactions. Mol.Cell, 18, 2005
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3FVM
| Crystal structure of Steptococcus suis mannonate dehydratase with metal Mn++ | 分子名称: | MANGANESE (II) ION, Mannonate dehydratase | 著者 | Peng, H, Zhang, Q.J, Gao, F, Liu, Y, Gao, F.G. | 登録日 | 2009-01-16 | 公開日 | 2009-09-01 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Crystal structures of Streptococcus suis mannonate dehydratase (ManD) and its complex with substrate: genetic and biochemical evidence for a catalytic mechanism J.Bacteriol., 191, 2009
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1Z7Q
| 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: | Potential proteasome component C5, Proteasome component C1, Proteasome component C11, ... | 著者 | Forster, A, Whitby, F.G, Hill, C.P. | 登録日 | 2005-03-26 | 公開日 | 2005-08-09 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (3.22 Å) | 主引用文献 | The 1.9 A structure of a proteasome-11S activator complex and implications for proteasome-PAN/PA700 interactions. Mol.Cell, 18, 2005
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2BLI
| L29W Mb deoxy | 分子名称: | MYOGLOBIN, PROTOPORPHYRIN IX CONTAINING FE | 著者 | Nienhaus, K, Ostermann, A, Nienhaus, G.U, Parak, F.G, Schmidt, M. | 登録日 | 2005-03-04 | 公開日 | 2005-04-06 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Ligand Migration and Protein Fluctuations in Myoglobin Mutant L29W Biochemistry, 44, 2005
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2BLJ
| Structure of L29W MbCO | 分子名称: | CARBON MONOXIDE, MYOGLOBIN, PROTOPORPHYRIN IX CONTAINING FE | 著者 | Nienhaus, K, Ostermann, A, Nienhaus, G.U, Parak, F.G, Schmidt, M. | 登録日 | 2005-03-04 | 公開日 | 2005-04-06 | 最終更新日 | 2024-05-08 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Ligand Migration and Protein Fluctuations in Myoglobin Mutant L29W Biochemistry, 44, 2005
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