Structure of Cyclophilin A in complex with 2,3-Diaminopyridine. Determined by X-ray diffraction at 1.25 Å resolution. Released 5 Apr 2017.
Explore 5LUD in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5-12 | 8 | 1 |
| β-strand | 15-24 | 10 | 1 |
| α-helix | 30-41 | 12 | |
| β-strand | 52 | 1 | 1 |
| β-strand | 55-57 | 3 | 1 |
| β-strand | 61-64 | 4 | 1 |
| β-strand | 77-78 | 2 | 2 |
| β-strand | 80 | 1 | 2 |
| β-strand | 83 | 1 | 3 |
| β-strand | 97-100 | 4 | 1 |
| β-strand | 108 | 1 | 3 |
| β-strand | 112-115 | 4 | 1 |
| α-helix | 120-122 | 3 | |
| β-strand | 128-134 | 7 | 1 |
| α-helix | 136-143 | 8 | |
| β-strand | 156-164 | 9 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Peptidyl-prolyl cis-trans isomerase | A | protein | 165 | Homo sapiens | P62937 (AlphaFold model) |
>5LUD_1 Peptidyl-prolyl cis-trans isomerase (chains A) MVNPTVFFDIAVDGEPLGRVSFELFADKVPKTAENFRALSTGEKGFGYKGSCFHRIIPGF MCQGGDFTRHNGTGGKSIYGEKFEDENFILKHTGPGILSMANAGPNTNGSQFFICTAKTE WLDGKHVVFGKVKEGMNIVEAMERFGSRNGKTSKKITIADCGQLE
| ID | Name | Formula | Copies |
|---|---|---|---|
| 76X | pyridine-2,3-diamine | C5 H7 N3 | 1 |
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:
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