KEGG   PATHWAY: cho03050
Entry
cho03050                    Pathway                                
Name
Proteasome - Cryptosporidium hominis
Description
The proteasome is a protein-destroying apparatus involved in many essential cellular functions, such as regulation of cell cycle, cell differentiation, signal transduction pathways, antigen processing for appropriate immune responses, stress signaling, inflammatory responses, and apoptosis. It is capable of degrading a variety of cellular proteins in a rapid and timely fashion and most substrate proteins are modified by ubiquitin before their degradation by the proteasome. The proteasome is a large protein complex consisting of a proteolytic core called the 20S particle and ancillary factors that regulate its activity in various ways. The most common form is the 26S proteasome containing one 20S core particle and two 19S regulatory particles that enable the proteasome to degrade ubiquitinated proteins by an ATP-dependent mechanism. Another form is the immunoproteasome containing two 11S regulatory particles, PA28 alpha and PA28 beta, which are induced by interferon gamma under the conditions of intensified immune response. Other regulatory particles include PA28 gamma and PA200. Although PA28 gamma also belongs to a family of activators of the 20S proteasome, it is localized within the nucleus and forms a homoheptamer. PA28 gamma has been implicated in the regulation of cell cycle progression and apoptosis. PA200 has been identified as a large nuclear protein that stimulates proteasomal hydrolysis of peptides.
Class
Genetic Information Processing; Folding, sorting and degradation
Pathway map
cho03050  Proteasome
cho03050

Other DBs
GO: 0000502
Organism
Cryptosporidium hominis [GN:cho]
Gene
Chro.80466  PCI domain [KO:K03033]
Chro.50142  proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 [KO:K06693]
Chro.10177  hypothetical protein [KO:K03035]
Chro.60414  26S proteasome non-ATPase regulatory subunit [KO:K03036]
Chro.70327  26S proteasome regulatory particle non-ATPase subunit8 [KO:K03038]
Chro.20114  26S proteasome subunit P40.5 [KO:K03039]
Chro.60380  Mov34/MPN/PAD-1 family proteasome regulatory subunit [KO:K03030]
Chro.20354  hypothetical protein [KO:K03031]
Chro.40069  26S proteasome regulatory subunit S5A [KO:K03029]
Chro.80073  26S proteasome regulatory subunit S2 (RPN1) [KO:K03028]
Chro.40452  PSMD1 protein [KO:K03032]
Chro.50345  hypothetical protein [KO:K06691]
Chro.60498  26S proteasome ATPase subunit [KO:K03061]
Chro.40138  26S proteasome AAA-ATPase subunit RPT2a [KO:K03062]
Chro.60119  hypothetical protein [KO:K03066]
Chro.80103  26S proteasome regulatory subunit [KO:K03064]
Chro.20147  26S protease subunit regulatory subunit 6a [KO:K03065]
Chro.40284  26S proteasome AAA-ATPase subunit RPT3 [KO:K03063]
Chro.80360  subunit of proteaseome activator complex [KO:K06697]
Chro.30254  20S proteasome subunit PAA1 [KO:K02730] [EC:3.4.25.1]
Chro.30255  20S proteasome alpha subunit A [KO:K02730] [EC:3.4.25.1]
Chro.70408  proteasome subunit alpha type 2 (20S proteasome alpha subunit B) (20S proteasome subunit alpha-2) [KO:K02726] [EC:3.4.25.1]
Chro.40039  proteasome subunit [KO:K02728] [EC:3.4.25.1]
Chro.20158  proteasome subunit alpha type 7 (Proteasome component DD5) [KO:K02731] [EC:3.4.25.1]
Chro.50200  proteasome subunit alpha type 5 [KO:K02729] [EC:3.4.25.1]
Chro.20222  proteasome A type subunit [KO:K02725] [EC:3.4.25.1]
Chro.30260  proteasome subunit alpha type 3 [KO:K02727] [EC:3.4.25.1]
Chro.20097  proteasome B type subunit [KO:K02738] [EC:3.4.25.1]
Chro.30293  proteasome component precursor [KO:K02739] [EC:3.4.25.1]
Chro.20061  proteasome component [KO:K02735] [EC:3.4.25.1]
Chro.10054  20S proteasome beta subunit D2 (PBD2) [KO:K02734] [EC:3.4.25.1]
Chro.50424  hypothetical protein [KO:K02737] [EC:3.4.25.1]
Chro.50050  beta tubulin [KO:K02736] [EC:3.4.25.1]
Reference
  Authors
Hirano Y, Murata S, Tanaka K
  Title
Large- and small-scale purification of mammalian 26S proteasomes.
  Journal
Methods Enzymol 399:227-40 (2005)
DOI:10.1016/S0076-6879(05)99015-0
Reference
  Authors
Saeki Y, Tanaka K
  Title
Cell biology: two hands for degradation.
  Journal
Nature 453:460-1 (2008)
DOI:10.1038/453460a
Reference
  Authors
Smith DM, Benaroudj N, Goldberg A
  Title
Proteasomes and their associated ATPases: a destructive combination.
  Journal
J Struct Biol 156:72-83 (2006)
DOI:10.1016/j.jsb.2006.04.012
Reference
  Authors
Strehl B, Seifert U, Kruger E, Heink S, Kuckelkorn U, Kloetzel PM
  Title
Interferon-gamma, the functional plasticity of the ubiquitin-proteasome system, and MHC class I antigen processing.
  Journal
Immunol Rev 207:19-30 (2005)
DOI:10.1111/j.0105-2896.2005.00308.x
Reference
  Authors
Darwin KH
  Title
Prokaryotic ubiquitin-like protein (Pup), proteasomes and pathogenesis.
  Journal
Nat Rev Microbiol 7:485-91 (2009)
DOI:10.1038/nrmicro2148
Reference
  Authors
Tomko RJ Jr, Hochstrasser M
  Title
Molecular architecture and assembly of the eukaryotic proteasome.
  Journal
Annu Rev Biochem 82:415-45 (2013)
DOI:10.1146/annurev-biochem-060410-150257
Reference
  Authors
Budenholzer L, Cheng CL, Li Y, Hochstrasser M
  Title
Proteasome Structure and Assembly.
  Journal
J Mol Biol 429:3500-3524 (2017)
DOI:10.1016/j.jmb.2017.05.027
Reference
  Authors
Cloos J, Roeten MS, Franke NE, van Meerloo J, Zweegman S, Kaspers GJ, Jansen G
  Title
(Immuno)proteasomes as therapeutic target in acute leukemia.
  Journal
Cancer Metastasis Rev 36:599-615 (2017)
DOI:10.1007/s10555-017-9699-4
Reference
  Authors
Sakata E, Bohn S, Mihalache O, Kiss P, Beck F, Nagy I, Nickell S, Tanaka K, Saeki Y, Forster F, Baumeister W
  Title
Localization of the proteasomal ubiquitin receptors Rpn10 and Rpn13 by electron cryomicroscopy.
  Journal
Proc Natl Acad Sci U S A 109:1479-84 (2012)
DOI:10.1073/pnas.1119394109
Related
pathway
cho04120  Ubiquitin mediated proteolysis
KO pathway
ko03050   

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