2XCJ
| Crystal structure of P2 C, the immunity repressor of temperate E. coli phage P2 | Descriptor: | C PROTEIN, FORMIC ACID, GLYCEROL, ... | Authors: | Massad, T, Skaar, K, Hogbom, M, Stenmark, P. | Deposit date: | 2010-04-23 | Release date: | 2010-07-28 | Last modified: | 2024-05-08 | Method: | X-RAY DIFFRACTION (1.8 Å) | Cite: | Crystal Structure of the P2 C-Repressor: A Binder of Non-Palindromic Direct DNA Repeats. Nucleic Acids Res., 38, 2010
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2L49
| The solution structure of the P2 C,the immunity repressor of the P2 bacteriophage | Descriptor: | C protein | Authors: | Massad, T, Papadopolos, E, Stenmark, P, Damberg, P. | Deposit date: | 2010-10-01 | Release date: | 2010-10-13 | Last modified: | 2024-05-01 | Method: | SOLUTION NMR | Cite: | The C repressor of the P2 bacteriophage. J.Biomol.Nmr, 64, 2016
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4LHF
| Crystal structure of a DNA binding protein from phage P2 | Descriptor: | Regulatory protein cox | Authors: | Berntsson, R.P.-A, Odegrip, R, Sehlen, W, Skaar, K, Svensson, L.M, Massad, T, Haggard-Ljungquist, E, Stenmark, P. | Deposit date: | 2013-07-01 | Release date: | 2014-03-05 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (2.401 Å) | Cite: | Structural insight into DNA binding and oligomerization of the multifunctional Cox protein of bacteriophage P2. Nucleic Acids Res., 42, 2014
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4IFG
| Crystal structure of TgCDPK1 with inhibitor bound | Descriptor: | 1-{(3R)-3-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl}prop-2-en-1-one, Calmodulin-domain protein kinase 1, UNKNOWN ATOM OR ION | Authors: | El Bakkouri, M, Tempel, W, Crandall, I, Massad, T, Loppnau, P, Graslund, S, Bountra, C, Arrowsmith, C.H, Edwards, A.M, Kain, K, Hui, R, Structural Genomics Consortium (SGC) | Deposit date: | 2012-12-14 | Release date: | 2014-04-16 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (2.11 Å) | Cite: | Crystal structure of TgCDPK1 with inhibitor bound To be Published
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4IHP
| Crystal structure of TgCDPK1 with inhibitor bound | Descriptor: | 1-tert-butyl-3-(3-chlorophenoxy)-1H-pyrazolo[3,4-d]pyrimidin-4-amine, Calmodulin-domain protein kinase 1, UNKNOWN ATOM OR ION | Authors: | El Bakkouri, M, Tempel, W, Crandall, I.E, Massad, T, Loppnau, P, Graslund, S, Bountra, C, Arrowsmith, C.H, Edwards, A.M, Kain, C.K, Shokat, K.M, Sibley, L.D, Hui, R, Structural Genomics Consortium (SGC) | Deposit date: | 2012-12-19 | Release date: | 2014-01-15 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (2.27 Å) | Cite: | Crystal structure of TgCDPK1 with inhibitor bound TO BE PUBLISHED
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4IH8
| Crystal structure of TgCDPK1 with inhibitor bound | Descriptor: | 4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl-cyclopentane, Calmodulin-domain protein kinase 1 | Authors: | El Bakkouri, M, Tempel, W, Crandall, I, Massad, T, Loppnau, P, Graslund, S, Bountra, C, Arrowsmith, C.H, Edwards, A.M, Kain, K, Hui, R, Structural Genomics Consortium (SGC) | Deposit date: | 2012-12-18 | Release date: | 2014-04-16 | Last modified: | 2024-02-28 | Method: | X-RAY DIFFRACTION (2.877 Å) | Cite: | Crystal structure of TgCDPK1 with inhibitor bound To be Published
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