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4CFG
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BU of 4cfg by Molmil
Structure of the TRIM25 coiled-coil
Descriptor: E3 UBIQUITIN/ISG15 LIGASE TRIM25
Authors:James, L.
Deposit date:2013-11-15
Release date:2014-12-10
Last modified:2024-10-23
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Structure of the Trim25 Coiled-Coil
To be Published
5LDN
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BU of 5ldn by Molmil
A viral capsid:antibody complex
Descriptor: Hexon protein,hexon capsid, antibody
Authors:James, L.
Deposit date:2016-06-27
Release date:2017-07-12
Last modified:2024-10-09
Method:X-RAY DIFFRACTION (2.7 Å)
Cite:Antibody-antigen kinetics constrain intracellular humoral immunity.
Sci Rep, 6, 2016
4RG2
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BU of 4rg2 by Molmil
Tudor Domain of Tumor suppressor p53BP1 with small molecule ligand
Descriptor: 1,2-ETHANEDIOL, 3-bromo-N-[3-(tert-butylamino)propyl]benzamide, Tumor suppressor p53-binding protein 1, ...
Authors:Dong, A, Mader, P, James, L, Perfetti, M, Tempel, W, Frye, S, Bountra, C, Arrowsmith, C.H, Edwards, A.M, Brown, P.J, Structural Genomics Consortium (SGC)
Deposit date:2014-09-29
Release date:2014-10-15
Last modified:2023-09-20
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Identification of a fragment-like small molecule ligand for the methyl-lysine binding protein, 53BP1.
ACS Chem. Biol., 10, 2015
8UGT
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BU of 8ugt by Molmil
E. eligens beta-glucuronidase bound to UNC10206581-G
Descriptor: 8-(4-beta-D-glucopyranuronosylpiperazin-1-yl)-5-(methylamino)-1,2,3,4-tetrahydro[1,2,3]triazino[4',5':4,5]thieno[2,3-c]isoquinoline, Beta-glucuronidase, GLYCEROL, ...
Authors:Simpson, J.B, Redinbo, M.R.
Deposit date:2023-10-06
Release date:2024-07-24
Last modified:2024-09-11
Method:X-RAY DIFFRACTION (2.65 Å)
Cite:Advanced piperazine-containing inhibitors target microbial beta-glucuronidases linked to gut toxicity.
Rsc Chem Biol, 5, 2024
3DPD
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BU of 3dpd by Molmil
Achieving multi-isoform PI3K inhibition in a series of substituted 3,4-Dihydro-2H-benzo[1,4]oxazines
Descriptor: 5,5-dimethyl-2-morpholin-4-yl-5,6-dihydro-1,3-benzothiazol-7(4H)-one, Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
Authors:Ceska, T.A.
Deposit date:2008-07-08
Release date:2008-08-26
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (2.85 Å)
Cite:Achieving multi-isoform PI3K inhibition in a series of substituted 3,4-dihydro-2H-benzo[1,4]oxazines
Bioorg.Med.Chem.Lett., 18, 2008

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