KEGG   PATHWAY: ehe04141
Entry
ehe04141                    Pathway                                
Name
Protein processing in endoplasmic reticulum - Encephalitozoon hellem
Description
The endoplasmic reticulum (ER) is a subcellular organelle where proteins are folded with the help of lumenal chaperones. Newly synthesized peptides enter the ER via the sec61 pore and are glycosylated. Correctly folded proteins are packaged into transport vesicles that shuttle them to the Golgi complex. Misfolded proteins are retained within the ER lumen in complex with molecular chaperones. Proteins that are terminally misfolded bind to BiP and are directed toward degradation through the proteasome in a process called ER-associated degradation (ERAD). Accumulation of misfolded proteins in the ER causes ER stress and activates a signaling pathway called the unfolded protein response (UPR). In certain severe situations, however, the protective mechanisms activated by the UPR are not sufficient to restore normal ER function and cells die by apoptosis.
Class
Genetic Information Processing; Folding, sorting and degradation
Pathway map
ehe04141  Protein processing in endoplasmic reticulum
ehe04141

Other DBs
GO: 0030433 0034976
Organism
Encephalitozoon hellem [GN:ehe]
Gene
EHEL_090110  ER translocation protein Sec61 [KO:K10956]
EHEL_090920  hypothetical protein [KO:K09481]
EHEL_050980  hypothetical protein [KO:K07342]
EHEL_070670  preprotein translocase subunit Sec62 [KO:K12275]
EHEL_060810  preprotein translocase subunit Sec63 [KO:K09540]
EHEL_040030  hypothetical protein [KO:K09523]
EHEL_091110  hypothetical protein [KO:K10082]
EHEL_050140  putative sar1 [KO:K07953] [EC:3.6.5.-]
EHEL_111340  hypothetical protein [KO:K14004]
EHEL_080130  hypothetical protein [KO:K14005]
EHEL_110670  Sec23-like protein transport protein [KO:K14006]
EHEL_021160  Sec23/Sec24-like protein [KO:K14007]
EHEL_021390  Sec23 domain-containing protein [KO:K14007]
EHEL_091570  protein disulfide isomerase [KO:K09580] [EC:5.3.4.1]
EHEL_020760  thioredoxin domain-containing protein [KO:K13984] [EC:5.3.4.1]
EHEL_040100  hypothetical protein [KO:K10950] [EC:1.8.4.-]
EHEL_050380  hypothetical protein [KO:K14009]
EHEL_111810  hypothetical protein [KO:K13989]
EHEL_011130  AAA+ ATPase [KO:K13525]
EHEL_070740  nuclear pore protein [KO:K14015]
EHEL_101200  ubiquitin fusion-degradation protein [KO:K14016]
EHEL_030430  heat shock protein 70 [KO:K03283]
EHEL_020040  hsp70-like protein [KO:K03283]
EHEL_070730  DnaJ-class molecular chaperone [KO:K09503]
EHEL_021030  heat shock protein 90 [KO:K04079]
EHEL_091760  hypothetical protein [KO:K14018]
EHEL_070250  hypothetical protein [KO:K04523]
EHEL_101770  hypothetical protein [KO:K04523]
EHEL_041140  ubiquitin fusion degradation protein 2 [KO:K10597] [EC:2.3.2.27]
EHEL_110810  translation initiation factor 2 subunit alpha [KO:K03237]
EHEL_060770  mRNA turnover and stability protein [KO:K10661] [EC:2.3.2.27]
EHEL_040530  ubiquitin-conjugating enzyme E2 [KO:K10575] [EC:2.3.2.23]
EHEL_010620  HRD ubiquitin ligase complex protein [KO:K10601] [EC:2.3.2.27]
EHEL_010980  SCF ubiquitin ligase and anaphase-promoting complex protein [KO:K03868] [EC:2.3.2.32]
EHEL_030180  SCF ubiquitin ligase Skp1-like protein [KO:K03094]
Compound
C00076  Calcium cation
G00009   
G00010   
G00011   
G00012   
G10694   
Reference
  Authors
Naidoo N
  Title
ER and aging-Protein folding and the ER stress response.
  Journal
Ageing Res Rev 8:150-9 (2009)
DOI:10.1016/j.arr.2009.03.001
Reference
  Authors
Malhotra JD, Kaufman RJ
  Title
The endoplasmic reticulum and the unfolded protein response.
  Journal
Semin Cell Dev Biol 18:716-31 (2007)
DOI:10.1016/j.semcdb.2007.09.003
Reference
  Authors
Maattanen P, Gehring K, Bergeron JJ, Thomas DY
  Title
Protein quality control in the ER: the recognition of misfolded proteins.
  Journal
Semin Cell Dev Biol 21:500-11 (2010)
DOI:10.1016/j.semcdb.2010.03.006
Reference
  Authors
Stolz A, Wolf DH
  Title
Endoplasmic reticulum associated protein degradation: a chaperone assisted journey to hell.
  Journal
Biochim Biophys Acta 1803:694-705 (2010)
DOI:10.1016/j.bbamcr.2010.02.005
Reference
  Authors
Dejgaard K, Theberge JF, Heath-Engel H, Chevet E, Tremblay ML, Thomas DY
  Title
Organization of the Sec61 translocon, studied by high resolution native electrophoresis.
  Journal
J Proteome Res 9:1763-71 (2010)
DOI:10.1021/pr900900x
Related
pathway
ehe03050  Proteasome
ehe03060  Protein export
KO pathway
ko04141   
LinkDB

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