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Induced myeloid leukemia cell differentiation protein fabcomplex in complex with AZD5991

Analyse Induced myeloid leukemia cell differentiation protein fabcomplex in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6FS0
Type
protein
Length
577 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Induced myeloid leukemia cell differentiation protein mcl- 1; Fab heavy chain; Fab light…
UniProt
Q07820
Ligands
E4W
Pockets
4 · best druggability 0.64

Structure

x-ray diffraction · 3 distinct chains · 26% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AInduced myeloid leukemia cell differentiation protein mcl- 1protein15678% helix, 0% strandQ07820
HFab heavy chainprotein2087% helix, 54% strand—
LFab light chainprotein2136% helix, 52% strand—

Ligands and binding sites

  • E4W · Azd5991 · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16190.640.7552empty
21640.580.8116E4W
31120.420.7726empty
4960.400.7718empty

Interfaces

3 interfaces between chains.

  • H–L · 1790 Ų buried · 10 hydrogen bonds · protein-protein
  • A–H · 721 Ų buried · 14 hydrogen bonds · protein-protein
  • A–L · 128 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6FS0 · Induced myeloid leukemia cell differentiation protein fabcomplex in complex with AZD5991 · the same entry in another collection · chain A against A, TM-score 1.00

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