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Structure of human pd-L1 in complex with macrocyclic inhibitor

Analyse Structure of human pd-L1 in complex with macrocyclic inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7OUN
Type
protein
Length
131 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Programmed cell death 1 ligand 1; Macrocyclic peptide
UniProt
Q9NZQ7

Structure

x-ray diffraction · 2 distinct chains · 9% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProgrammed cell death 1 ligand 1protein11710% helix, 48% strandQ9NZQ7
BMacrocyclic peptideprotein140% helix, 43% strand—

Interfaces

1 interface between chains.

  • A–B · 486 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 7OUN · Structure of human PD-L1 in complex with macrocyclic inhibitor · the same entry in another collection · chain A against A, TM-score 1.00

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