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8C12

Identification of an intermediate activation state of PAK5 reveals a novel mechanism of kinase inhibition.

This is a non-PDB format compatible entry.
Summary for 8C12
Entry DOI10.2210/pdb8c12/pdb
DescriptorSerine/threonine-protein kinase PAK 5, PAK5-Af17 (3 entities in total)
Functional Keywordskinase, pak5, affimer, urothelial cancer., transferase
Biological sourceHomo sapiens (human)
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Total number of polymer chains2
Total formula weight46055.12
Authors
Martin, H.L.,Turner, A.L.,Trinh, C.H.,Bayliss, R.W.,Tomlinson, D.C. (deposition date: 2022-12-19, release date: 2023-10-25)
Primary citationMartin, H.L.,Turner, A.L.,Higgins, J.,Tang, A.A.,Tiede, C.,Taylor, T.,Siripanthong, S.,Adams, T.L.,Manfield, I.W.,Bell, S.M.,Morrison, E.E.,Bond, J.,Trinh, C.H.,Hurst, C.D.,Knowles, M.A.,Bayliss, R.W.,Tomlinson, D.C.
Affimer-mediated locking of p21-activated kinase 5 in an intermediate activation state results in kinase inhibition.
Cell Rep, 42:113184-113184, 2023
Cited by
PubMed: 37776520
DOI: 10.1016/j.celrep.2023.113184
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.549 Å)
Structure validation

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