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8WJY
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BU of 8wjy by Molmil
PKMYT1_Cocrystal_Cpd 4
Descriptor: DIMETHYL SULFOXIDE, GLYCEROL, Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase, ...
Authors:Wang, Y, Wang, C, Liu, T, Qi, H, Chen, S, Cai, X, Zhang, M, Aliper, A, Ren, F, Ding, X, Zhavoronkov, A.
Deposit date:2023-09-26
Release date:2023-11-22
Last modified:2024-05-29
Method:X-RAY DIFFRACTION (1.88 Å)
Cite:Discovery of Tetrahydropyrazolopyrazine Derivatives as Potent and Selective MYT1 Inhibitors for the Treatment of Cancer.
J.Med.Chem., 67, 2024
8J1K
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BU of 8j1k by Molmil
co-crystal structure of non-carboxylic acid inhibitor with PHD2
Descriptor: Egl nine homolog 1, MANGANESE (II) ION, N-[(6-cyanopyridin-3-yl)methyl]-5-oxidanyl-2-[(3R)-3-oxidanylpyrrolidin-1-yl]-1,7-naphthyridine-6-carboxamide
Authors:Xu, J, Fu, Y, Ding, X, Meng, Q, Wang, L, Zhang, M, Ding, X, Ren, F, Zhavoronkov, A.
Deposit date:2023-04-13
Release date:2024-04-17
Method:X-RAY DIFFRACTION (2.451 Å)
Cite:co-crystal structure of non-carboxylic acid inhibitor with PHD2
To Be Published
8XAM
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BU of 8xam by Molmil
Co-crystal structure of compound 7 in complex with MAT2A
Descriptor: 2-[3-[7-chloranyl-4-(dimethylamino)-2-oxidanylidene-quinazolin-1-yl]phenoxy]-~{N}-[3-[7-chloranyl-4-(dimethylamino)-2-oxidanylidene-quinazolin-1-yl]phenyl]ethanamide, S-ADENOSYLMETHIONINE, S-adenosylmethionine synthase isoform type-2
Authors:Gao, F, Ding, X.
Deposit date:2023-12-04
Release date:2024-02-28
Method:X-RAY DIFFRACTION (1.3 Å)
Cite:Discovery of novel MAT2A inhibitors by an allosteric site-compatible fragment growing approach.
Bioorg.Med.Chem., 100, 2024
8Y0V
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BU of 8y0v by Molmil
HIF prolyl hydroxylase 2 in complex with inhibitor
Descriptor: Egl nine homolog 1, MANGANESE (II) ION, ~{tert}-butyl 4-[6-[(6-cyanopyridin-3-yl)methylcarbamoyl]-5-oxidanyl-1,7-naphthyridin-2-yl]piperazine-1-carboxylate
Authors:Ding, X, Fan, Y.
Deposit date:2024-01-23
Release date:2024-12-18
Last modified:2024-12-25
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Intestinal mucosal barrier repair and immune regulation with an AI-developed gut-restricted PHD inhibitor.
Nat.Biotechnol., 2024

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