Structure
atLeast majority ProS Experiment
:order disorder conflict PDB cluster ProS Pfam Domain SEG
358
order/disorder by at least rule
disorder by at least rule
order/disorder by majority rule
Region 1gol A 1-1 disorder
Region 1gol A 2-358 order
Region 2erk A 1-5 disorder
Region 2erk A 6-358 order
Region 2z7l A 1-15 disorder
Region 2z7l A 16-31 order
Region 2z7l A 32-34 disorder
Region 2z7l A 35-327 order
Region 2z7l A 328-335 disorder
Region 2z7l A 336-355 order
Region 2z7l A 356-358 disorder
Region 3c9w A 2-5 disorder
Region 3c9w A 6-174 order
Region 3c9w A 175-187 disorder
Region 3c9w A 188-354 order
Region 3c9w A 355-358 disorder
Region 3c9w B 2-5 disorder
Region 3c9w B 6-174 order
Region 3c9w B 175-187 disorder
Region 3c9w B 188-354 order
Region 3c9w B 355-358 disorder
Region 3erk A 1-5 disorder
Region 3erk A 6-355 order
Region 3erk A 356-358 disorder
Region 1erk A 1-1 disorder
Region 1erk A 2-358 order
Seq 1-358 Hetero dimer : IID50334 Complex
Region 3o71 A 1-8 disorder
Region 3o71 A 9-174 order
Region 3o71 A 175-179 disorder
Region 3o71 A 180-200 order
Region 3o71 A 201-201 disorder
Region 3o71 A 202-354 order
Region 3o71 A 355-358 disorder
Seq 2-358 Hetero dimer : IID00617 Complex
Region 2gph A 2-9 disorder
Region 2gph A 10-354 order
Region 2gph A 355-358 disorder
Seq 2-358 Hetero dimer : IID50335 Complex
Region 2fys B 2-7 disorder
Region 2fys B 8-175 order
Region 2fys B 176-183 disorder
Region 2fys B 184-328 order
Region 2fys B 329-332 disorder
Region 2fys B 333-357 order
Region 2fys B 358-358 disorder
Region 2fys A 2-7 disorder
Region 2fys A 8-200 order
Region 2fys A 201-201 disorder
Region 2fys A 202-356 order
Region 2fys A 357-358 disorder
27-27 Phosphoserine; by SGK1
188-188 Phosphothreonine; by autocatalysis
Prediction
Disorder 1-7,180-184,357-358
Function
Function in SwissProt
Acts as a transcriptional repressor. Binds to a [GC]AAA[GC] consensus sequence. Repress the expression of interferon gamma-induced genes. Seems to bind to the promoter of CCL5, DMP1, IFIH1, IFITM1, IRF7, IRF9, LAMP3, OAS1, OAS2, OAS3 and STAT1. Transcriptional activity is independent of kinase activity.