5LUD: Cyclophilin A

Structure of Cyclophilin A in complex with 2,3-Diaminopyridine. Determined by X-ray diffraction at 1.25 Å resolution. Released 5 Apr 2017.

Method
X-ray diffraction
Resolution
1.25 Å
Organism
Homo sapiens
Chains
1
Atoms
1,549
Mol. weight
18.15 kDa
Ligands
76X
Released
5 Apr 2017

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

Secondary structure: helices and β-sheets

5LUD contains 3 α-helices and 13 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: 3 helices, 13 β-strands

ElementResiduesLengthSheet
β-strand5-1281
β-strand15-24101
α-helix30-4112
β-strand5211
β-strand55-5731
β-strand61-6441
β-strand77-7822
β-strand8012
β-strand8313
β-strand97-10041
β-strand10813
β-strand112-11541
α-helix120-1223
β-strand128-13471
α-helix136-1438
β-strand156-16491

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Peptidyl-prolyl cis-trans isomeraseAprotein165Homo sapiensP62937 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5LUD_1 Peptidyl-prolyl cis-trans isomerase (chains A)
MVNPTVFFDIAVDGEPLGRVSFELFADKVPKTAENFRALSTGEKGFGYKGSCFHRIIPGF
MCQGGDFTRHNGTGGKSIYGEKFEDENFILKHTGPGILSMANAGPNTNGSQFFICTAKTE
WLDGKHVVFGKVKEGMNIVEAMERFGSRNGKTSKKITIADCGQLE

Ligands and cofactors

IDNameFormulaCopies
76Xpyridine-2,3-diamineC5 H7 N31

Primary citation

Thermo-kinetic analysis space expansion for cyclophilin-ligand interactions - identification of a new nonpeptide inhibitor using BiacoreTM T200. Wear, M.A., Nowicki, M.W., Blackburn, E.A. et al. FEBS Open Bio (2017) 7:533-549. DOI 10.1002/2211-5463.12201 · PubMed

Other PDB entries of the same protein (UniProt P62937 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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