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3VN9
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BU of 3vn9 by Molmil
Rifined Crystal structure of non-phosphorylated MAP2K6 in a putative auto-inhibition state
Descriptor: 9-{5-O-[(R)-hydroxy{[(S)-hydroxy(phosphonoamino)phosphoryl]oxy}phosphoryl]-beta-L-ribofuranosyl}-9H-purin-6-amine, Dual specificity mitogen-activated protein kinase kinase 6, MAGNESIUM ION
Authors:Kinoshita, T, Matsuzaka, H, Nakai, R, Kirii, Y, Yokota, K, Tada, T, Matsumoto, T.
Deposit date:2012-01-05
Release date:2012-02-29
Last modified:2023-11-08
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Crystal structure of non-phosphorylated MAP2K6 in a putative auto-inhibition state
J.Biochem., 151, 2012
3VUG
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BU of 3vug by Molmil
Crystal structure of a cysteine-deficient mutant M2 in MAP kinase JNK1
Descriptor: Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1, SULFATE ION
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-06-28
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (3.24 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
3VUD
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BU of 3vud by Molmil
Crystal structure of a cysteine-deficient mutant M1 in MAP kinase JNK1
Descriptor: Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1, SULFATE ION
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-06-28
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (3.5 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
3VUM
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BU of 3vum by Molmil
Crystal structure of a cysteine-deficient mutant M7 in MAP kinase JNK1
Descriptor: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1, ...
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-07-02
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (2.69 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
3VUH
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BU of 3vuh by Molmil
Crystal structure of a cysteine-deficient mutant M3 in MAP kinase JNK1
Descriptor: GLYCEROL, Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1, ...
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-06-28
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (2.7 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
3VUL
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BU of 3vul by Molmil
Crystal structure of a cysteine-deficient mutant M1 in MAP kinase JNK1
Descriptor: Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-07-02
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (2.81 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
3VUK
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BU of 3vuk by Molmil
Crystal structure of a cysteine-deficient mutant M5 in MAP kinase JNK1
Descriptor: Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1, SULFATE ION
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-07-02
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (2.95 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
3A4O
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BU of 3a4o by Molmil
Lyn kinase domain
Descriptor: STAUROSPORINE, Tyrosine-protein kinase Lyn
Authors:Miyano, N, Kinoshita, T, Tada, T.
Deposit date:2009-07-11
Release date:2009-12-08
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (3 Å)
Cite:Structural basis for the inhibitor recognition of human Lyn kinase domain
Bioorg.Med.Chem.Lett., 19, 2009
3VUI
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BU of 3vui by Molmil
Crystal structure of a cysteine-deficient mutant M2 in MAP kinase JNK1
Descriptor: Mitogen-activated protein kinase 8, Peptide from C-Jun-amino-terminal kinase-interacting protein 1, SULFATE ION
Authors:Nakaniwa, T, Kinoshita, T, Inoue, T.
Deposit date:2012-06-28
Release date:2013-02-13
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Seven cysteine-deficient mutants depict the interplay between thermal and chemical stabilities of individual cysteine residues in mitogen-activated protein kinase c-Jun N-terminal kinase 1
Biochemistry, 51, 2012
7CE4
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BU of 7ce4 by Molmil
Tankyrase2 catalytic domain in complex with K-476
Descriptor: 5-[3-[[1-(6,7-dimethoxyquinazolin-4-yl)piperidin-4-yl]methyl]-2-oxidanylidene-4H-quinazolin-1-yl]-2-fluoranyl-benzenecarbonitrile, Poly [ADP-ribose] polymerase tankyrase-2, SULFATE ION, ...
Authors:Takahashi, Y, Suzuki, M, Saito, J.
Deposit date:2020-06-22
Release date:2021-05-12
Last modified:2023-11-29
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:The dual pocket binding novel tankyrase inhibitor K-476 enhances the efficacy of immune checkpoint inhibitor by attracting CD8 + T cells to tumors.
Am J Cancer Res, 11, 2021
5ETY
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BU of 5ety by Molmil
Crystal Structure of human Tankyrase-1 bound to K-756
Descriptor: 3-[[1-(6,7-dimethoxyquinazolin-4-yl)piperidin-4-yl]methyl]-1,4-dihydroquinazolin-2-one, Tankyrase-1, ZINC ION
Authors:Takahashi, Y, Miyagi, H, Suzuki, M, Saito, J.
Deposit date:2015-11-18
Release date:2016-06-22
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (2.9 Å)
Cite:The Discovery and Characterization of K-756, a Novel Wnt/ beta-Catenin Pathway Inhibitor Targeting Tankyrase
Mol.Cancer Ther., 15, 2016

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PDB entries from 2024-07-03

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