6X8H
| Caspase-8 in complex with AOMK inhibitor, Ac-DW3-KE, forms tetrahedral adduct | 分子名称: | Ac-DW3-KE, Caspase-8 | 著者 | Solania, A, Xu, J.H, Wolan, D.W. | 登録日 | 2020-06-01 | 公開日 | 2021-06-02 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (1.48 Å) | 主引用文献 | Caspase-8 in complex with AOMK inhibitor, Ac-DW3-KE, forms tetrahedral adduct To Be Published
|
|
6X8L
| |
6X8J
| |
6X8I
| |
6X8K
| |
4AFP
| The structure of metacaspase 2 from T. brucei determined in the presence of Samarium | 分子名称: | METACASPASE MCA2, SAMARIUM (III) ION | 著者 | McLuskey, K, Rudolf, J, Isaacs, N.W, Coombs, G.H, Moss, C.X, Mottram, J.C. | 登録日 | 2012-01-23 | 公開日 | 2012-05-02 | 最終更新日 | 2017-07-05 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Crystal Structure of a Trypanosoma Brucei Metacaspase. Proc.Natl.Acad.Sci.USA, 109, 2012
|
|
4ZVU
| |
4ZVQ
| |
4DCP
| Crystal Structure of caspase 3, L168F mutant | 分子名称: | Caspase Inhibitor AC-DEVD-CHO, Caspase-3 subunit p12, Caspase-3 subunit p17 | 著者 | Chung, S.J, Kang, H.J, Kim, S.J. | 登録日 | 2012-01-18 | 公開日 | 2012-12-12 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Molecular insight into the role of the leucine residue on the L2 loop in the catalytic activity of caspases 3 and 7 Biosci.Rep., 32, 2012
|
|
4ZVS
| |
4ZVO
| |
4DCJ
| Crystal structure of caspase 3, L168D mutant | 分子名称: | Caspase Inhibitor AC-DEVD-CHO, Caspase-3 subunit p12, Caspase-3 subunit p17 | 著者 | Chung, S.J, Kang, H.J, Kim, S.J. | 登録日 | 2012-01-17 | 公開日 | 2012-12-12 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Molecular insight into the role of the leucine residue on the L2 loop in the catalytic activity of caspases 3 and 7 Biosci.Rep., 32, 2012
|
|
4DCO
| Crystal Structure of caspase 3, L168Y mutant | 分子名称: | Caspase Inhibitor AC-DEVD-CHO, Caspase-3 subunit p12, Caspase-3 subunit p17 | 著者 | Chung, S.J, Kang, H.J, Kim, S.J. | 登録日 | 2012-01-18 | 公開日 | 2012-12-12 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Molecular insight into the role of the leucine residue on the L2 loop in the catalytic activity of caspases 3 and 7 Biosci.Rep., 32, 2012
|
|
4EHA
| Allosteric Modulation of Caspase-3 through Mutagenesis | 分子名称: | ACE-ASP-GLU-VAL-ASP-CHLOROMETHYLKETONE INHIBITOR, Caspase-3 | 著者 | Walters, J, Schipper, J.L, Swartz, P.D, Mattos, C, Clark, A.C. | 登録日 | 2012-04-02 | 公開日 | 2012-06-06 | 最終更新日 | 2017-11-15 | 実験手法 | X-RAY DIFFRACTION (1.696 Å) | 主引用文献 | Allosteric modulation of caspase 3 through mutagenesis. Biosci.Rep., 32, 2012
|
|
4EHH
| Allosteric Modulation of Caspase-3 through Mutagenesis | 分子名称: | ACE-ASP-GLU-VAL-ASP-CHLOROMETHYLKETONE INHIBITOR, Caspase-3 | 著者 | Walters, J, Schipper, J.L, Swartz, P.D, Mattos, C, Clark, A.C. | 登録日 | 2012-04-02 | 公開日 | 2012-06-06 | 最終更新日 | 2017-11-15 | 実験手法 | X-RAY DIFFRACTION (1.78 Å) | 主引用文献 | Allosteric modulation of caspase 3 through mutagenesis. Biosci.Rep., 32, 2012
|
|
1M72
| Crystal Structure of Caspase-1 from Spodoptera frugiperda | 分子名称: | 1,2-ETHANEDIOL, Ace-Asp-Glu-Val-Asp-chloromethylketone, Caspase-1 | 著者 | Forsyth, C.M, Lemongello, D, Friesen, P.D, Fisher, A.J. | 登録日 | 2002-07-18 | 公開日 | 2004-01-20 | 最終更新日 | 2013-02-27 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Crystal structure of an invertebrate caspase. J.Biol.Chem., 279, 2004
|
|
6KN1
| |
6KMT
| P32 of caspase-11 mutant C254A | 分子名称: | Caspase-4 | 著者 | Ding, J, Sun, Q. | 登録日 | 2019-08-01 | 公開日 | 2020-03-11 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Structural Mechanism for GSDMD Targeting by Autoprocessed Caspases in Pyroptosis. Cell, 180, 2020
|
|
6KMU
| |
1NME
| Structure of Casp-3 with tethered salicylate | 分子名称: | 2-HYDROXY-5-(2-MERCAPTO-ETHYLSULFAMOYL)-BENZOIC ACID, 3-(2-MERCAPTO-ACETYLAMINO)-4-OXO-PENTANOIC ACID, Caspase-3 | 著者 | Erlanson, D.A, Lam, J, Wiesmann, C, Luong, T.N, Simmons, B, DeLano, W, Choong, I.C, Flanagan, M, Lee, D, O'Brian, T. | 登録日 | 2003-01-09 | 公開日 | 2003-03-11 | 最終更新日 | 2023-08-16 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | In situ assembly of enzyme inhibitors using extended tethering. Nat.Biotechnol., 21, 2003
|
|
2XZT
| Caspase-3 in Complex with DARPin-3.4_I78S | 分子名称: | (4R)-2-METHYLPENTANE-2,4-DIOL, CASPASE-3, DARPIN-3.4_I78S | 著者 | Barandun, J, Schroeder, T, Mittl, P, Grutter, M.G. | 登録日 | 2010-11-29 | 公開日 | 2011-12-14 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Caspase-3 in Complex with Darpin-3.4_I78S To be Published
|
|
2XYP
| Caspase-3:CAS26049945 | 分子名称: | CASPASE-3 SUBUNIT P12, CASPASE-3 SUBUNIT P17, PHENYLMETHYL N-[(2S)-4-CHLORO-3-OXO-1-PHENYL-BUTAN-2-YL]CARBAMATE | 著者 | Ganesan, R, Jelakovic, S, Grutter, M.G, Mittl, P.R. | 登録日 | 2010-11-18 | 公開日 | 2011-08-17 | 最終更新日 | 2017-06-28 | 実験手法 | X-RAY DIFFRACTION (1.86 Å) | 主引用文献 | In Silico Identification and Crystal Structure Validation of Caspase-3 Inhibitors without a P1 Aspartic Acid Moiety. Acta Crystallogr.,Sect.F, 67, 2011
|
|
2XYG
| Caspase-3:CAS329306 | 分子名称: | CASPASE-3 SUBUNIT P12, CASPASE-3 SUBUNIT P17, N-[(2S)-4-chloro-3-oxo-1-phenyl-butan-2-yl]-4-methyl-benzenesulfonamide | 著者 | Ganesan, R, Jelakovic, S, Grutter, M.G, Mittl, P.R. | 登録日 | 2010-11-17 | 公開日 | 2011-08-17 | 実験手法 | X-RAY DIFFRACTION (1.54 Å) | 主引用文献 | In Silico Identification and Crystal Structure Validation of Caspase-3 Inhibitors without a P1 Aspartic Acid Moiety. Acta Crystallogr.,Sect.F, 67, 2011
|
|
2XZD
| Caspase-3 in Complex with an Inhibitory DARPin-3.4 | 分子名称: | (4R)-2-METHYLPENTANE-2,4-DIOL, (4S)-2-METHYL-2,4-PENTANEDIOL, CASPASE-3, ... | 著者 | Barandun, J, Schroeder, T, Mittl, P, Grutter, M.G. | 登録日 | 2010-11-24 | 公開日 | 2011-12-14 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Specific Inhibition of Caspase-3 by a Competitive Darpin: Molecular Mimicry between Native and Designed Inhibitors. Structure, 21, 2013
|
|
2Y0B
| Caspase-3 in Complex with an Inhibitory DARPin-3.4_S76R | 分子名称: | (4R)-2-METHYLPENTANE-2,4-DIOL, (4S)-2-METHYL-2,4-PENTANEDIOL, CASPASE-3, ... | 著者 | Barandun, J, Schroeder, T, Mittl, P, Grutter, M.G. | 登録日 | 2010-12-01 | 公開日 | 2011-12-21 | 最終更新日 | 2023-12-20 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Specific Inhibition of Caspase-3 by a Competitive Darpin: Molecular Mimicry between Native and Designed Inhibitors. Structure, 21, 2013
|
|