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MolNFT v1 · #116224 · protein

Crystal structure of human FKBD25 in complex with FK506

5D75 · Peptidyl-prolyl cis-trans isomerase FKBP3: “Crystal structure of human FKBD25 in complex with FK506”. X-ray diffraction, 2 ligands (JEF, FK5), 1 pocket (best druggability 0.37). MolNFT v1 #116224 on GenesisL1: 3D structure, binding…

PDB
5D75
Type
protein
Length
120 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptidyl-prolyl cis-trans isomerase FKBP3
EC
5.2.1.8
UniProt
Q00688
Ligands
JEF, FK5
Pockets
1 · best druggability 0.37

Structure

x-ray diffraction · 1 distinct chain · 8% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptidyl-prolyl cis-trans isomerase FKBP3 (EC 5.2.1.8)protein1208% helix, 37% strandQ00688

Ligands and binding sites

  • JEF · O-(O-(2-aminopropyl)-O'-(2-methoxyethyl)polypropylene glycol 500) · ligand · 2 copies · chains A
  • FK5 · 8-deethyl-8-[but-3-enyl]-ascomycin · ligand · chains A

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

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1700.370.7714empty

Compared structures

  • 5D75 · Crystal structure of Human FKBD25 in complex with FK506 · the same entry in another collection · chain A against A, TM-score 1.00
  • Q00688 · AlphaFold monomer V2.0 prediction for peptidyl-prolyl cis-trans isomerase FKBP3 (Q00688) · a predicted model of the same protein · chain A against A, TM-score 0.94

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