Search Keyword:


Search option:


IID00363
UniprotO95863
ProteinZinc finger protein SNAI1
GeneSNAI1
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
264
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 1-264 Hetero dimer : IID00386Complex
 Evidence X-RAY 3w5k B Reference
       Region 3w5k B 1-152 disorder
       Region 3w5k B 153-204 order
       Region 3w5k B 205-206 disorder
       Region 3w5k B 207-264 order
Seqdisorder 2-21
 Evidence CD Reference
       Region 2-21 disorder
Seq 2-21 Hetero trimer : IID00009Complex
 Evidence X-RAY 2y48 C Reference
       Region 2y48 C 2-10 order
       Region 2y48 C 11-21 disorder
Seq 175-180 Hetero tetramer : IID00301Complex
 Evidence X-RAY 4qli B Reference
       Region 4qli B 175-180 order
SeqProS verified 2-10 Hetero trimer : IID00009Complex
       Region 2y48 C 2-10 order
       Region 2-21 disorder
Seqphosphorylation
    203-203 Phosphothreonine; by LATS2
    92-92 Phosphoserine; by CK2
    96-96 Phosphoserine
    100-100 Phosphoserine
    104-104 Phosphoserine
    107-107 Phosphoserine
    111-111 Phosphoserine
    115-115 Phosphoserine
    119-119 Phosphoserine
    82-82 Phosphoserine
    246-246 Phosphoserine; by PAK1
    11-11 Phosphoserine; by PKA
 
Prediction
NeProc
Disorder 1-150,257-264
Order 151-256
ProS 1-65,93-150,257-264
AlphaFold
Disorder 1-152,158-158,174-197,199-209,211-212,214-215,217-219,229-236,258-264
Order 153-157,159-173,198-198,210-210,213-213,216-216,220-228,237-257
Pfam Hmmer
PF00096 154-176 0.0002
PF00096 180-202 2e-05
PF00096 208-230 2.8e-07
PF00096 236-259 0.0002
SEG 100-120
Function
Function in SwissProt
Involved in induction of the epithelial to mesenchymal transition (EMT), formation and maintenance of embryonic mesoderm, growth arrest, survival and cell migration. Binds to 3 E-boxes of the E-cadherin/CDH1 gene promoter and to the promoters of CLDN7 and KRT8 and, in association with histone demethylase KDM1A which it recruits to the promoters, causes a decrease in dimethylated H3K4 levels and represses transcription (PubMed:20389281, PubMed:20562920). The N-terminal SNAG domain competes with histone H3 for the same binding site on the histone demethylase complex formed by KDM1A and RCOR1, and thereby inhibits demethylation of histone H3 at 'Lys-4' (in vitro) (PubMed:20389281, PubMed:21300290, PubMed:23721412). During EMT, involved with LOXL2 in negatively regulating pericentromeric heterochromatin transcription (By similarity). SNAI1 recruits LOXL2 to pericentromeric regions to oxidize histone H3 and repress transcription which leads to release of heterochromatin component CBX5/HP1A, enabling chromatin reorganization and acquisition of mesenchymal traits (By similarity). Associates with EGR1 and SP1 to mediate tetradecanoyl phorbol acetate (TPA)-induced up-regulation of CDKN2B, possibly by binding to the CDKN2B promoter region 5'-TCACA-3. In addition, may also activate the CDKN2B promoter by itself.