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Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: (2R,5S,11S,14S,18E)-2,11-dimethyl-14-(propan-2-yl)-3-oxa- 9,12,15,21,29-PENTAAZATETRACYCLO[18.5.3.1~5,9~.0~23,27~]NONACOSA- 1(26),18,20,22,24,27-hexaene-4,10,13,16-tetrone (compound 21)

Analyse Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6X4O
Type
protein
Length
163 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptidyl-prolyl cis-trans isomerase a
EC
5.2.1.8
UniProt
P62937
Ligands
UO7

Structure

x-ray diffraction · 1 distinct chain · 14% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptidyl-prolyl cis-trans isomerase a (EC 5.2.1.8)protein16314% helix, 33% strandP62937

Ligands and binding sites

  • UO7 · (2R,5S,11S,14S,18E)-2,11-dimethyl-14-(propan-2-yl)-3-oxa-9,12,15,21,29-pentaazatetracyclo[18.5.3.1~5, 9~.0~23,27~]nonacosa-1(26),18,20,22,24,27-hexaene-4, 10,13,16-tetrone · ligand · chains A

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

Compared structures

  • 6X4O · Human cyclophilin A bound to a series of acylcic and macrocyclic inhibitors… · the same entry in another collection · chain A against A, TM-score 1.00

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