4ZQK
Structure of the complex of human programmed death-1 (PD-1) and its ligand PD-L1.
Summary for 4ZQK
Entry DOI | 10.2210/pdb4zqk/pdb |
Descriptor | Programmed cell death 1 ligand 1, Programmed cell death protein 1, SODIUM ION, ... (4 entities in total) |
Functional Keywords | complex, co-stimulation, receptor-ligand complex, immune system |
Biological source | Homo sapiens (Human) More |
Cellular location | Isoform 1: Cell membrane; Single-pass type I membrane protein. Isoform 2: Endomembrane system; Single-pass type I membrane protein: Q9NZQ7 Membrane; Single-pass type I membrane protein: Q15116 |
Total number of polymer chains | 2 |
Total formula weight | 26385.79 |
Authors | Zak, K.M.,Dubin, G.,Holak, T.A. (deposition date: 2015-05-10, release date: 2015-11-04, Last modification date: 2024-10-16) |
Primary citation | Zak, K.M.,Kitel, R.,Przetocka, S.,Golik, P.,Guzik, K.,Musielak, B.,Domling, A.,Dubin, G.,Holak, T.A. Structure of the Complex of Human Programmed Death 1, PD-1, and Its Ligand PD-L1. Structure, 23:2341-2348, 2015 Cited by PubMed Abstract: Targeting the PD-1/PD-L1 immunologic checkpoint with monoclonal antibodies has recently provided breakthrough progress in the treatment of melanoma, non-small cell lung cancer, and other types of cancer. Small-molecule drugs interfering with this pathway are highly awaited, but their development is hindered by insufficient structural information. This study reveals the molecular details of the human PD-1/PD-L1 interaction based on an X-ray structure of the complex. First, it is shown that the ligand binding to human PD-1 is associated with significant plasticity within the receptor. Second, a detailed molecular map of the interaction surface is provided, allowing definition of the regions within both interacting partners that may likely be targeted by small molecules. PubMed: 26602187DOI: 10.1016/j.str.2015.09.010 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.45 Å) |
Structure validation
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