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8TLZ

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

Summary for 8TLZ
Entry DOI10.2210/pdb8tlz/pdb
DescriptorMHC class I polypeptide-related sequence A, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, (2S)-2-hydroxybutanedioic acid, ... (6 entities in total)
Functional Keywordsmodified mica, ligand nkg2d, immune system
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight46044.19
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 (2.75 Å)
Structure validation

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