5OBK: The Fk1 domain of FKBP51

The Fk1 domain of FKBP51 in complex with (1S,5S,6R)-10-((3,5-dichlorophenyl)sulfonyl)-5-(hydroxymethyl)-3-(pyridin-2-ylmethyl)-3,10-diazabicyclo[4.3.1]decan-2-one. Determined by X-ray diffraction at 1.0 Å resolution. Released 4 Apr 2018.

Method
X-ray diffraction
Resolution
1.0 Å
Organism
Homo sapiens
Chains
1
Atoms
1,358
Mol. weight
14.51 kDa
Ligands
9QN
Released
4 Apr 2018

Explore 5OBK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5OBK contains 6 α-helices and 9 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 6 helices, 9 β-strands

ElementResiduesLengthSheet
α-helix14-218
β-strand23-2421
β-strand33-3971
α-helix47-482
β-strand52-6091
β-strand66-6941
α-helix71-733
β-strand77-8041
α-helix88-958
α-helix97-982
β-strand102-10761
α-helix109-1113
β-strand11812
β-strand12212
β-strand128-138111

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Peptidyl-prolyl cis-trans isomerase FKBP5Aprotein128Homo sapiensQ13451 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5OBK_1 Peptidyl-prolyl cis-trans isomerase FKBP5 (chains A)
GAPATVTEQGEDITSKKDRGVLKIVKRVGNGEETPMIGDKVYVHYKGKLSNGKKFDSSHD
RNEPFVFSLGKGQVIKAWDIGVATMKKGEICHLLCKPEYAYGSAGSLPKIPSNATLFFEI
ELLDFKGE

Ligands and cofactors

IDNameFormulaCopies
9QN(1~{S},5~{S},6~{R})-10-[3,5-bis(chloranyl)phenyl]sulfonyl-5-(hydroxymethyl)-3-(…C21 H23 Cl2 N3 O4 S1

Primary citation

Chemogenomic Profiling of Human and Microbial FK506-Binding Proteins. Pomplun, S., Sippel, C., Hahle, A. et al. J Med Chem (2018) 61:3660-3673. DOI 10.1021/acs.jmedchem.8b00137 · PubMed

Other PDB entries of the same protein (UniProt Q13451 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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