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IID00569
UniprotQ16637
ProteinSurvival motor neuron protein
GeneSMN1
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
294
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 26-51 Hetero dimer : IID00524Complex
 Evidence NMR 2leh B Reference
       Region 2leh B 26-51 order
       Region 2leh B 26-32 high_rmsd
Seq 82-169 Monomer :
 Evidence X-RAY 4qq6 A Reference
       Region 4qq6 A 82-89 disorder
       Region 4qq6 A 90-147 order
 Evidence NMR 1g5v A Reference
       Region 1g5v A 82-89 disorder
       Region 1g5v A 90-145 order
       Region 1g5v A 146-169 disorder
 Evidence NMR 4a4e A Reference
       Region 4a4e A 84-147 order
       Region 4a4e A 84-86 high_rmsd
 Evidence X-RAY 1mhn A Reference
       Region 1mhn A 89-147 order
 Evidence NMR 4a4g A Reference
       Region 4a4g A 84-147 order
       Region 4a4g A 84-85 high_rmsd
Seq 263-294 Homo dimer : IID90020Complex
 Evidence X-RAY 4gli A Reference
       Region 4gli A 263-281 order
       Region 4gli A 282-294 disorder
Seqphosphorylation
    31-31 Phosphoserine
    187-187 Phosphoserine; by PKA
    85-85 Phosphothreonine; by PKA
    69-69 Phosphothreonine
    28-28 Phosphoserine
    25-25 Phosphothreonine
    8-8 Phosphoserine; by PKA
    5-5 Phosphoserine; by PKA
    4-4 Phosphoserine; by PKA
Seqacetylation
    2-2 N-acetylalanine
 
Prediction
NeProc
Disorder 1-13,50-86,147-266,285-294
Order 14-24,30-49,87-146,267-284
ProS 9-13,50-57,147-162,167-174,186-192,228-234,257-266,285-294
AlphaFold
Disorder 1-18,20-21,24-32,57-90,146-195,197-198,200-217,219-219,225-255,283-283,285-294
Order 19-19,22-23,33-56,91-145,196-196,199-199,218-218,220-224,256-282,284-284
Pfam Hmmer
PF06003 26-293 3.5e-128
SEG 4-11 ,65-88 ,147-166 ,194-251
Function
Function in SwissProt
The SMN complex plays a catalyst role in the assembly of small nuclear ribonucleoproteins (snRNPs), the building blocks of the spliceosome. Thereby, plays an important role in the splicing of cellular pre-mRNAs. Most spliceosomal snRNPs contain a common set of Sm proteins SNRPB, SNRPD1, SNRPD2, SNRPD3, SNRPE, SNRPF and SNRPG that assemble in a heptameric protein ring on the Sm site of the small nuclear RNA to form the core snRNP. In the cytosol, the Sm proteins SNRPD1, SNRPD2, SNRPE, SNRPF and SNRPG are trapped in an inactive 6S pICln-Sm complex by the chaperone CLNS1A that controls the assembly of the core snRNP. Dissociation by the SMN complex of CLNS1A from the trapped Sm proteins and their transfer to an SMN-Sm complex triggers the assembly of core snRNPs and their transport to the nucleus. Ensures the correct splicing of U12 intron-containing genes that may be important for normal motor and proprioceptive neurons development. Also required for resolving RNA-DNA hybrids created by RNA polymerase II, that form R-loop in transcription terminal regions, an important step in proper transcription termination. May also play a role in the metabolism of small nucleolar ribonucleoprotein (snoRNPs).