CPLM 1.0 - Compendium of Protein Lysine Modification
TagContent
CPLM ID CPLM-000265
UniProt Accession
Genbank Protein ID
Genbank Nucleotide ID
Protein Name
 Torsin-1A 
Protein Synonyms/Alias
 Dystonia 1 protein; Torsin family 1 member A 
Gene Name
 TOR1A 
Gene Synonyms/Alias
 DQ2; DYT1 
Created Date
 July 27, 2013 
Organism
 Homo sapiens (Human) 
NCBI Taxa ID
 9606 
Lysine Modification
Position
Peptide
Type
References
53FAECCGQKRSLSREAubiquitination[1]
309EEMTFFPKEERVFSDubiquitination[1, 2]
325GCKTVFTKLDYYYDDubiquitination[2]
Reference
 [1] Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments.
 Udeshi ND, Svinkina T, Mertins P, Kuhn E, Mani DR, Qiao JW, Carr SA.
 Mol Cell Proteomics. 2013 Mar;12(3):825-31. [PMID: 23266961]
 [2] Systematic and quantitative assessment of the ubiquitin-modified proteome.
 Kim W, Bennett EJ, Huttlin EL, Guo A, Li J, Possemato A, Sowa ME, Rad R, Rush J, Comb MJ, Harper JW, Gygi SP.
 Mol Cell. 2011 Oct 21;44(2):325-40. [PMID: 21906983
Functional Description
 May serve as a molecular chaperone assisting in the proper folding of secreted and/or membrane proteins. In the nucleus, displaces the nuclear membrane proteins SUN2, SYNE2 and SYNE3, leaving nuclear pores and SUN1 unchanged. 
Sequence Annotation
 NP_BIND 102 109 ATP.
 CARBOHYD 143 143 N-linked (GlcNAc...) (high mannose).
 CARBOHYD 158 158 N-linked (GlcNAc...) (high mannose).  
Keyword
 Alternative splicing; ATP-binding; Chaperone; Complete proteome; Disease mutation; Dystonia; Endoplasmic reticulum; Glycoprotein; Membrane; Nucleotide-binding; Nucleus; Polymorphism; Reference proteome; Signal. 
Sequence Source
 UniProt (SWISSPROT/TrEMBL); GenBank; EMBL 
Protein Length
 332 AA 
Protein Sequence
MKLGRAVLGL LLLAPSVVQA VEPISLGLAL AGVLTGYIYP RLYCLFAECC GQKRSLSREA 60
LQKDLDDNLF GQHLAKKIIL NAVFGFINNP KPKKPLTLSL HGWTGTGKNF VSKIIAENIY 120
EGGLNSDYVH LFVATLHFPH ASNITLYKDQ LQLWIRGNVS ACARSIFIFD EMDKMHAGLI 180
DAIKPFLDYY DLVDGVSYQK AMFIFLSNAG AERITDVALD FWRSGKQRED IKLKDIEHAL 240
SVSVFNNKNS GFWHSSLIDR NLIDYFVPFL PLEYKHLKMC IRVEMQSRGY EIDEDIVSRV 300
AEEMTFFPKE ERVFSDKGCK TVFTKLDYYY DD 332 
Gene Ontology
 GO:0005788; C:endoplasmic reticulum lumen; IDA:MGI.
 GO:0031965; C:nuclear membrane; IEA:UniProtKB-SubCell.
 GO:0005524; F:ATP binding; TAS:ProtInc.
 GO:0004252; F:serine-type endopeptidase activity; TAS:ProtInc.
 GO:0051082; F:unfolded protein binding; TAS:ProtInc.
 GO:0051085; P:chaperone mediated protein folding requiring cofactor; IEA:InterPro.
 GO:0071763; P:nuclear membrane organization; IEA:Compara.
 GO:0006457; P:protein folding; TAS:ProtInc.
 GO:0051260; P:protein homooligomerization; IDA:MGI.
 GO:0006986; P:response to unfolded protein; TAS:ProtInc. 
Interpro
 IPR027417; P-loop_NTPase.
 IPR010448; Torsin.
 IPR017378; Torsin_subgr. 
Pfam
 PF06309; Torsin 
SMART
  
PROSITE
  
PRINTS