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Crystal structure of the E493V mutant of human apoptosis inducing factor (aif)

Analyse Crystal structure of the E493V mutant of human apoptosis inducing factor (aif) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4FDC
Type
protein
Length
461 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Apoptosis-inducing factor 1, mitochondrial
EC
1.-.-.-
UniProt
O95831
Ligands
FAD
Pockets
3 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BApoptosis-inducing factor 1, mitochondrial (EC 1.-.-.-)protein46127% helix, 30% strandO95831

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19770.820.8388FAD
2630.320.7618empty
3540.260.7416empty

Compared structures

  • 4FDC · Crystal structure of the E493V mutant of human apoptosis inducing factor (AIF) · the same entry in another collection · chain B against B, TM-score 1.00
  • O95831 · AlphaFold monomer V2.0 prediction for apoptosis-inducing factor 1, mitochondrial (O95831) · a predicted model of the same protein · chain B against A, TM-score 1.00

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