4OGN: E3 ubiquitin-protein ligase Mdm2

Co-Crystal Structure of MDM2 with Inhbitor Compound 3. Determined by X-ray diffraction at 1.38 Å resolution. Released 2 Apr 2014.

Method
X-ray diffraction
Resolution
1.38 Å
Organism
Homo sapiens
Chains
1
Atoms
1,012
Mol. weight
12.89 kDa
Ligands
2U5
Released
2 Apr 2014

Explore 4OGN in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4OGN contains 5 α-helices and 5 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 5 helices, 5 β-strands

ElementResiduesLengthSheet
α-helix23-253
β-strand27-3041
α-helix32-409
β-strand48-4921
α-helix50-6314
β-strand74-7632
α-helix81-866
β-strand90-9232
α-helix96-1049
β-strand107-10931

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
E3 ubiquitin-protein ligase Mdm2Aprotein105Homo sapiensQ00987 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4OGN_1 E3 ubiquitin-protein ligase Mdm2 (chains A)
MSVPTDGAVTTSQIPASEQETLVRPKPLLLKLLKSVGAQKDTYTMKEVLFYLGQYIMTKR
LYDEKQQHIVYCSNDLLGDLFGVPSFSVKEHRKIYTMIYRNLVVV

Ligands and cofactors

IDNameFormulaCopies
2U56-{[(3R,5R,6S)-1-[(1S)-2-(tert-butylsulfonyl)-1-cyclopropylethyl]-5-(3-chloroph…C34 H38 Cl2 N2 O5 S1

Water and common crystallization additives (SO4) are not listed.

Primary citation

Novel Inhibitors of the MDM2-p53 Interaction Featuring Hydrogen Bond Acceptors as Carboxylic Acid Isosteres. Gonzalez, A.Z., Li, Z., Beck, H.P. et al. J Med Chem (2014) 57:2963-2988. DOI 10.1021/jm401911v · PubMed

Other PDB entries of the same protein (UniProt Q00987 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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