GL1X · GenesisL1 explorer

Research workbench

Cereblon isoform 4 from magnetospirillum gryphiswaldense in complex with aminoglutethimide

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
5OH1
Type
protein
Length
309 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cereblon isoform 4
UniProt
A4TVL0
Ligands
EF2, 9UQ, ZN
Pockets
6 · best druggability 0.52

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ACereblon isoform 4protein1056% helix, 51% strandA4TVL0
BCereblon isoform 4protein1049% helix, 50% strandA4TVL0
CCereblon isoform 4protein1006% helix, 51% strandA4TVL0

Ligands and binding sites

  • EF2 · S-Thalidomide · ligand · 2 copies · chains A, B
  • 9UQ · (3~{R})-3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione · ligand · chains 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12220.520.7737empty
2720.510.8520empty
3660.400.7915EF2
4580.400.8011EF2
5590.350.77149UQ

Interfaces

2 interfaces between chains.

  • A–B · 538 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 474 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 5OH1 · Cereblon isoform 4 from Magnetospirillum gryphiswaldense in complex with Aminoglutethimide · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.