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8DCP

PI 3-kinase alpha with nanobody 3-126

Summary for 8DCP
Entry DOI10.2210/pdb8dcp/pdb
EMDB information27327
DescriptorPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform, Phosphatidylinositol 3-kinase regulatory subunit alpha (3 entities in total)
Functional Keywordsphosphoinositide 3-kinase (pi3k), activation, inhibition, nanobody, conformational changes, structural protein, transferase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight211445.78
Authors
Primary citationHart, J.R.,Liu, X.,Pan, C.,Liang, A.,Ueno, L.,Xu, Y.,Quezada, A.,Zou, X.,Yang, S.,Zhou, Q.,Schoonooghe, S.,Hassanzadeh-Ghassabeh, G.,Xia, T.,Shui, W.,Yang, D.,Vogt, P.K.,Wang, M.W.
Nanobodies and chemical cross-links advance the structural and functional analysis of PI3K alpha.
Proc.Natl.Acad.Sci.USA, 119:e2210769119-e2210769119, 2022
Cited by
PubMed Abstract: Nanobodies and chemical cross-linking were used to gain information on the identity and positions of flexible domains of PI3Kα. The application of chemical cross-linking mass spectrometry (CXMS) facilitated the identification of the p85 domains BH, cSH2, and SH3 as well as their docking positions on the PI3Kα catalytic core. Binding of individual nanobodies to PI3Kα induced activation or inhibition of enzyme activity and caused conformational changes that could be correlated with enzyme function. Binding of nanobody Nb3-126 to the BH domain of p85α substantially improved resolution for parts of the PI3Kα complex, and binding of nanobody Nb3-159 induced a conformation of PI3Kα that is distinct from known PI3Kα structures. The analysis of CXMS data also provided mechanistic insights into the molecular underpinning of the flexibility of PI3Kα.
PubMed: 36095215
DOI: 10.1073/pnas.2210769119
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.41 Å)
Structure validation

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