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IID50401
UniprotQ8VEB2
ProteinProtein salvador homolog 1
GeneSav1
OrganismMus musculus
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
386
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 196-272 Hetero dimer : IID50398Complex
 Evidence X-RAY 7bqg A Reference
       Region 7bqg A 196-198 disorder
       Region 7bqg A 199-272 order
Seq 196-285 Monomer :
 Evidence X-RAY 7bqf A Reference
       Region 7bqf A 196-198 disorder
       Region 7bqf A 199-282 order
       Region 7bqf A 283-285 disorder
Seq 198-233 Monomer :
 Evidence NMR 2ysb A Reference
       Region 2ysb A 198-233 order
Seq 231-266 Homo dimer :
 Evidence NMR 2dwv B Reference
       Region 2dwv B 231-266 order
       Region 2dwv B 231-234 high_rmsd
 Evidence NMR 2dwv A Reference
       Region 2dwv A 231-266 order
       Region 2dwv A 231-234 high_rmsd
Seqphosphorylation
    211-211 Phosphothreonine
    137-137 Phosphoserine
    95-95 Phosphoserine
 
Prediction
NeProc
Disorder 1-200,275-294,373-386
Order 201-274,295-372
ProS 5-37,116-120,135-142,156-161,169-173,285-294,373-386
AlphaFold
Disorder 1-200,231-239,267-292,381-386
Order 201-230,240-266,293-380
Pfam Hmmer
PF00397 202-231 9.3e-11
PF00397 237-266 4.5e-07
SEG 276-287
Function
Function in SwissProt
Regulator of STK3/MST2 and STK4/MST1 in the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. The core of this pathway is composed of a kinase cascade wherein STK3/MST2 and STK4/MST1, in complex with its regulatory protein SAV1, phosphorylates and activates LATS1/2 in complex with its regulatory protein MOB1, which in turn phosphorylates and inactivates YAP1 oncoprotein and WWTR1/TAZ. Phosphorylation of YAP1 by LATS1/2 inhibits its translocation into the nucleus to regulate cellular genes important for cell proliferation, cell death, and cell migration. SAV1 is required for STK3/MST2 and STK4/MST1 activation and promotes cell-cycle exit and terminal differentiation in developing epithelial tissues. Plays a role in centrosome disjunction by regulating the localization of NEK2 to centrosomes, and its ability to phosphorylate CROCC and CEP250. In conjunction with STK3/MST2, activates the transcriptional activity of ESR1 through the modulation of its phosphorylation (By similarity).