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Cereblon isoform 4 from magnetospirillum gryphiswaldense in complex with piperidin-2-one (valerolactam)

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
5OHB
Type
protein
Length
313 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cereblon isoform 4
UniProt
A4TVL0
Ligands
V1L, ZN
Pockets
5 · best druggability 0.53

Structure

x-ray diffraction · 3 distinct chains · 7% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACereblon isoform 4protein1066% helix, 51% strandA4TVL0
BCereblon isoform 4protein1059% helix, 52% strandA4TVL0
CCereblon isoform 4protein1026% helix, 51% strandA4TVL0

Ligands and binding sites

  • V1L · piperidin-2-one · ligand · 3 copies · chains A, B, C
  • ZN · Zinc ion · metal · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11920.530.7833empty
2580.440.8416empty
3810.440.8016empty
4570.370.7813V1L
5550.260.7214empty

Interfaces

2 interfaces between chains.

  • A–B · 546 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 500 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5OHB · Cereblon isoform 4 from Magnetospirillum gryphiswaldense in complex with Piperidin-2-one… · the same entry in another collection · chain A against A, TM-score 1.00

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