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Cereblon isoform 4 from magnetospirillum gryphiswaldense in complex with avadomide (cc-122)

Analyse Cereblon isoform 4 from magnetospirillum gryphiswaldense in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7PSO
Type
protein
Length
318 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cereblon isoform 4
UniProt
A4TVL0
Ligands
EF2, 835, ZN, PO4
Pockets
5 · best druggability 0.63

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACereblon isoform 4protein1088% helix, 48% strandA4TVL0
BCereblon isoform 4protein1049% helix, 50% strandA4TVL0
CCereblon isoform 4protein1066% helix, 51% strandA4TVL0

Ligands and binding sites

  • EF2 · S-Thalidomide · ligand · 2 copies · chains A, B
  • 835 · (3S)-3-(5-azanyl-2-methyl-4-oxidanylidene-quinazolin-3-yl)piperidine-2,6-dione · ligand · chains C
  • ZN · Zinc ion · metal · 3 copies · chains A, B, C
  • PO4 · Phosphate ion · ion · 3 copies · chains A, B, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12320.630.8231empty
22040.510.7741empty
3600.390.7915EF2
4520.350.7811835
5680.270.7312empty

Interfaces

2 interfaces between chains.

  • A–B · 613 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 474 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 7PSO · Cereblon isoform 4 from Magnetospirillum gryphiswaldense in complex with Avadomide… · the same entry in another collection · chain A against A, TM-score 1.00

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