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4D0M

Phosphatidylinositol 4-kinase III beta in a complex with Rab11a-GTP- gamma-S and the Rab-binding domain of FIP3

Summary for 4D0M
Entry DOI10.2210/pdb4d0m/pdb
Related1OIV 1OIW 1OIX 1YZK 2HV8 4C4P 4D0L
DescriptorPHOSPHATIDYLINOSITOL 4-KINASE BETA, RAS-RELATED PROTEIN RAB-11A, RAB11 FAMILY-INTERACTING PROTEIN 3, ... (6 entities in total)
Functional Keywordsphosphoinositide, phosphatidylinositol 4-kinase, lipid kinase, family of rab interacting proteins, fip3, rab-binding domain, rbd, rab11, gtp, pik93, golgi, recycling endosome, signaling protein
Biological sourceHOMO SAPIENS (HUMAN)
More
Total number of polymer chains36
Total formula weight1149872.98
Authors
Burke, J.E.,Inglis, A.J.,Perisic, O.,Masson, G.R.,McLaughlin, S.H.,Rutaganira, F.,Shokat, K.M.,Williams, R.L. (deposition date: 2014-04-29, release date: 2014-05-28, Last modification date: 2023-12-20)
Primary citationBurke, J.E.,Inglis, A.J.,Perisic, O.,Masson, G.R.,Mclaughlin, S.H.,Rutaganira, F.,Shokat, K.M.,Williams, R.L.
Structures of Pi4Kiiibeta Complexes Show Simultaneous Recruitment of Rab11 and its Effectors.
Science, 344:1035-, 2014
Cited by
PubMed Abstract: Phosphatidylinositol 4-kinases (PI4Ks) and small guanosine triphosphatases (GTPases) are essential for processes that require expansion and remodeling of phosphatidylinositol 4-phosphate (PI4P)-containing membranes, including cytokinesis, intracellular development of malarial pathogens, and replication of a wide range of RNA viruses. However, the structural basis for coordination of PI4K, GTPases, and their effectors is unknown. Here, we describe structures of PI4Kβ (PI4KIIIβ) bound to the small GTPase Rab11a without and with the Rab11 effector protein FIP3. The Rab11-PI4KIIIβ interface is distinct compared with known structures of Rab complexes and does not involve switch regions used by GTPase effectors. Our data provide a mechanism for how PI4KIIIβ coordinates Rab11 and its effectors on PI4P-enriched membranes and also provide strategies for the design of specific inhibitors that could potentially target plasmodial PI4KIIIβ to combat malaria.
PubMed: 24876499
DOI: 10.1126/SCIENCE.1253397
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (6 Å)
Structure validation

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