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8TM2

Preclinical Characterization of Pan-NKG2D Ligand-Binding NKG2D Receptor Decoys

Summary for 8TM2
Entry DOI10.2210/pdb8tm2/pdb
DescriptorNKG2-D type II integral membrane protein, MHC class I polypeptide-related sequence A, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total)
Functional Keywordscomplex mica variant, linked nkg2d, immune system
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight54476.12
Authors
Rupert, P.B.,Strong, R. (deposition date: 2023-07-27, release date: 2024-04-17, Last modification date: 2024-11-13)
Primary citationRupert, P.B.,Buerger, M.,Girard, E.J.,Frutoso, M.,Parrilla, D.,Ng, K.,Gooley, T.,Groh, V.,Strong, R.K.
Preclinical characterization of Pan-NKG2D ligand-binding NKG2D receptor decoys.
Heliyon, 10:e28583-e28583, 2024
Cited by
PubMed Abstract: NKG2D and its ligands are critical regulators of protective immune responses controlling infections and cancer, defining a crucial immune signaling axis. Current therapeutic efforts targeting this axis almost exclusively aim at enhancing NKG2D-mediated effector functions. However, this axis can drive disease processes when dysregulated, in particular, driving stem-like cancer cell reprogramming and tumorigenesis through receptor/ligand self-stimulation on tumor cells. Despite complexities with its structure and biology, we developed multiple novel engineered proteins that functionally serve as axis-blocking NKG2D "decoys" and report biochemical, structural, , and evaluation of their functionality.
PubMed: 38586421
DOI: 10.1016/j.heliyon.2024.e28583
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.85 Å)
Structure validation

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