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Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: tert-butyl [(2S)-1-{[(3S,17S)-2,16-dioxo-10,15-dioxa-1, 21-DIAZATRICYCLO[15.3.1.1~5,9~]DOCOSA-5(22),6,8-trien-3-YL]AMINO}-3- methyl-1-oxobutan-2-YL]CARBAMATE (compound 3)

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
6X4M
Type
protein
Length
167 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
UMM
Pockets
1 · best druggability 0.32

Structure

x-ray diffraction · 1 distinct chain · 14% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptidyl-prolyl cis-trans isomerase a (EC 5.2.1.8)protein16714% helix, 32% strandP62937

Ligands and binding sites

  • UMM · Tert-butyl [(2S)-1-{[(3S,17S)-2,16-dioxo-10,15-dioxa-1, 21-diazatricyclo[15.3.1.1~5,9~]docosa-5(22),6,8-trien-3-yl]amino}-3-methyl-1-oxobutan-2-yl]carbamate · 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
1700.320.7516UMM

Compared structures

  • 6X4M · Human cyclophilin A bound to a series of acylcic and macrocyclic inhibitors: tert-butyl… · the same entry in another collection · chain A against A, TM-score 1.00

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