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MolNFT v1 · #58922 · protein

Crystal structures of FMS1 in complex with its inhibitors

3BI4 · Polyamine oxidase FMS1: “Crystal structures of FMS1 in complex with its inhibitors”. X-ray diffraction, 2 ligands (FAD, 298), 8 pockets (best druggability 0.87). MolNFT v1 #58922 on GenesisL1: 3D structure, binding sites and pockets…

PDB
3BI4
Type
protein
Length
993 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Polyamine oxidase FMS1
EC
1.5.3.11
UniProt
P50264
Ligands
FAD, 298
Pockets
8 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APolyamine oxidase FMS1 (EC 1.5.3.11)protein49737% helix, 21% strandP50264
BPolyamine oxidase FMS1 (EC 1.5.3.11)protein49637% helix, 20% strandP50264

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
  • 298 · N-[(1E,2Z)-but-2-en-1-ylidene]-N'-[(2E)-but-2-en-1-ylidene]butane-1,4-diamine · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16010.870.9291FAD, 298
24510.860.9376FAD, 298
31790.480.7628empty
41450.450.7624empty
5760.430.8015empty

Interfaces

1 interface between chains.

  • A–B · 1546 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 3BI4 · Crystal structures of fms1 in complex with its inhibitors · the same entry in another collection · chain A against A, TM-score 1.00
  • P50264 · AlphaFold monomer V2.0 prediction for polyamine oxidase FMS1 (P50264) · a predicted model of the same protein · chain B against A, TM-score 0.99

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