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Switch #:
SWTI000354
Switch type:
Avidity-sensing

Description:
Phosphorylation of two 14-3-3-binding motifs in RAF proto-oncogene serine/threonine-protein kinase (RAF1) in response to growth factors induces high-avidity binding to dimeric 14-3-3 protein zeta/delta (YWHAZ), with pS621 being the high-affinity interaction site. This interaction locks RAF proto-oncogene serine/threonine-protein kinase (RAF1) in an inhibited conformation.

Participants:
(1) 14-3-3 protein zeta/delta (YWHAZ)
(2) RAF proto-oncogene serine/threonine-protein kinase (RAF1)

Interactions
This is a sequential switch. The interactions in this switch take place in a defined order. The order is defined by numbers to the left of each interaction. More than one interaction can occur in each step, these interactions occur independently but are necessary for future step
2Interaction #2 RAF1 - Interaction #1 YWHAZ - YWHAZ

Requires Interaction #1 YWHAZ - YWHAZ

Interfaces
(3) LIG_14-3-3_1 motif (256RSTSTP261) in RAF proto-oncogene serine/threonine-protein kinase (RAF1)
(4) Interaction #1 YWHAZ - YWHAZ

Interaction Regulation
PTM-dependent Induction (Phosphorylation of S259 on RAF proto-oncogene serine/threonine-protein kinase (RAF1)) of the RAF proto-oncogene serine/threonine-protein kinase (RAF1) LIG_14-3-3_1 motif - 14-3-3 protein interaction

Regulatory Enzymes for switch
Modifying enzymes for residue: S259: RAC-alpha serine/threonine-protein kinase (AKT1)

Context
References

(1) Dynamic changes in C-Raf phosphorylation and 14-3-3 protein binding in response to growth factor stimulation: differential roles of 14-3-3 protein binding sites.
Hekman et al. J. Biol. Chem. (2004)

(2) Phosphorylation and regulation of Raf by Akt (protein kinase B).
Zimmermann et al. Science (1999)

See also

Other switches involving participants
14-3-3 protein zeta/delta (YWHAZ) - 11 more (view)
RAF proto-oncogene serine/threonine-protein kinase (RAF1) - 1 more (view)

Other switches involving interfaces
14-3-3 protein - 38 more (view)
LIG_14-3-3_1 - 13 more (view)




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