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2024-04-23 18:10:29, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002794 4759 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens proteasome (prosome, macropain) subunit, beta type, 2
(PSMB2), transcript variant 1, mRNA.
ACCESSION NM_002794
VERSION NM_002794.4 GI:315139001
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 4759)
AUTHORS Collavoli,A., Comelli,L., Cervelli,T. and Galli,A.
TITLE The over-expression of the beta2 catalytic subunit of the
proteasome decreases homologous recombination and impairs DNA
double-strand break repair in human cells
JOURNAL J. Biomed. Biotechnol. 2011, 757960 (2011)
PUBMED 21660142
REMARK GeneRIF: Results showed that the overexpression of beta2 subunit
decreased homologous recombination in human cells without altering
the cell proteasome activity and the Rad51p level.
REFERENCE 2 (bases 1 to 4759)
AUTHORS Oh,J.H., Yang,J.O., Hahn,Y., Kim,M.R., Byun,S.S., Jeon,Y.J.,
Kim,J.M., Song,K.S., Noh,S.M., Kim,S., Yoo,H.S., Kim,Y.S. and
Kim,N.S.
TITLE Transcriptome analysis of human gastric cancer
JOURNAL Mamm. Genome 16 (12), 942-954 (2005)
PUBMED 16341674
REFERENCE 3 (bases 1 to 4759)
AUTHORS Listovsky,T., Oren,Y.S., Yudkovsky,Y., Mahbubani,H.M., Weiss,A.M.,
Lebendiker,M. and Brandeis,M.
TITLE Mammalian Cdh1/Fzr mediates its own degradation
JOURNAL EMBO J. 23 (7), 1619-1626 (2004)
PUBMED 15029244
REFERENCE 4 (bases 1 to 4759)
AUTHORS Conticello,S.G., Harris,R.S. and Neuberger,M.S.
TITLE The Vif protein of HIV triggers degradation of the human
antiretroviral DNA deaminase APOBEC3G
JOURNAL Curr. Biol. 13 (22), 2009-2013 (2003)
PUBMED 14614829
REFERENCE 5 (bases 1 to 4759)
AUTHORS Yu,X., Yu,Y., Liu,B., Luo,K., Kong,W., Mao,P. and Yu,X.F.
TITLE Induction of APOBEC3G ubiquitination and degradation by an HIV-1
Vif-Cul5-SCF complex
JOURNAL Science 302 (5647), 1056-1060 (2003)
PUBMED 14564014
REFERENCE 6 (bases 1 to 4759)
AUTHORS Coux,O., Tanaka,K. and Goldberg,A.L.
TITLE Structure and functions of the 20S and 26S proteasomes
JOURNAL Annu. Rev. Biochem. 65, 801-847 (1996)
PUBMED 8811196
REMARK Review article
REFERENCE 7 (bases 1 to 4759)
AUTHORS Kristensen,P., Johnsen,A.H., Uerkvitz,W., Tanaka,K. and Hendil,K.B.
TITLE Human proteasome subunits from 2-dimensional gels identified by
partial sequencing
JOURNAL Biochem. Biophys. Res. Commun. 205 (3), 1785-1789 (1994)
PUBMED 7811265
REMARK Erratum:[Biochem Biophys Res Commun. 1995 Feb 27;207(3):1059. PMID:
7864893]
REFERENCE 8 (bases 1 to 4759)
AUTHORS Nothwang,H.G., Tamura,T., Tanaka,K. and Ichihara,A.
TITLE Sequence analyses and inter-species comparisons of three novel
human proteasomal subunits, HsN3, HsC7-I and HsC10-II, confine
potential proteolytic active-site residues
JOURNAL Biochim. Biophys. Acta 1219 (2), 361-368 (1994)
PUBMED 7918633
REFERENCE 9 (bases 1 to 4759)
AUTHORS Rasmussen,H.H., van Damme,J., Puype,M., Gesser,B., Celis,J.E. and
Vandekerckhove,J.
TITLE Microsequences of 145 proteins recorded in the two-dimensional gel
protein database of normal human epidermal keratinocytes
JOURNAL Electrophoresis 13 (12), 960-969 (1992)
PUBMED 1286667
REFERENCE 10 (bases 1 to 4759)
AUTHORS Dawson,S.J. and White,L.A.
TITLE Treatment of Haemophilus aphrophilus endocarditis with
ciprofloxacin
JOURNAL J. Infect. 24 (3), 317-320 (1992)
PUBMED 1602151
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL354864.16, BC101836.1,
AL157951.5 and BM664618.1.
On Dec 17, 2010 this sequence version replaced gi:22538463.
Summary: The proteasome is a multicatalytic proteinase complex with
a highly ordered ring-shaped 20S core structure. The core structure
is composed of 4 rings of 28 non-identical subunits; 2 rings are
composed of 7 alpha subunits and 2 rings are composed of 7 beta
subunits. Proteasomes are distributed throughout eukaryotic cells
at a high concentration and cleave peptides in an
ATP/ubiquitin-dependent process in a non-lysosomal pathway. An
essential function of a modified proteasome, the immunoproteasome,
is the processing of class I MHC peptides. This gene encodes a
member of the proteasome B-type family, also known as the T1B
family, that is a 20S core beta subunit. Multiple alternatively
spliced transcript variants encoding distinct isoforms have been
found for this gene. [provided by RefSeq, Dec 2010].
Transcript Variant: This variant (1) encodes the longest isoform
(1).
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: BM476538.1, BM469736.1 [ECO:0000332]
RNAseq introns :: mixed/partial sample support
ERS025081, ERS025082 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-368 AL354864.16 172406-172773
369-1051 BC101836.1 1-683
1052-4390 AL157951.5 5907-9245
4391-4759 BM664618.1 1-369 c
FEATURES Location/Qualifiers
source 1..4759
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="1"
/map="1p34.2"
gene 1..4759
/gene="PSMB2"
/gene_synonym="HC7-I"
/note="proteasome (prosome, macropain) subunit, beta type,
2"
/db_xref="GeneID:5690"
/db_xref="HGNC:9539"
/db_xref="HPRD:03708"
/db_xref="MIM:602175"
exon 1..503
/gene="PSMB2"
/gene_synonym="HC7-I"
/inference="alignment:Splign:1.39.8"
variation 8
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:60306926"
variation 32
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="g"
/db_xref="dbSNP:57991211"
misc_feature 95..97
/gene="PSMB2"
/gene_synonym="HC7-I"
/note="upstream in-frame stop codon"
variation 189
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:58935459"
variation 196
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="g"
/db_xref="dbSNP:567476"
variation 216
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="c"
/db_xref="dbSNP:58724360"
variation 267
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace=""
/replace="a"
/db_xref="dbSNP:56926147"
variation 304
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace=""
/replace="t"
/db_xref="dbSNP:60039597"
STS 369..1051
/gene="PSMB2"
/gene_synonym="HC7-I"
/db_xref="UniSTS:486264"
variation 393
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:11550442"
CDS 413..1018
/gene="PSMB2"
/gene_synonym="HC7-I"
/EC_number="3.4.25.1"
/note="isoform 1 is encoded by transcript variant 1;
macropain subunit C7-I; multicatalytic endopeptidase
complex subunit C7-1; proteasome component C7-I;
proteasome subunit, beta type, 2; proteasome subunit beta
type-2; proteasome beta 2 subunit; multicatalytic
endopeptidase complex subunit C7-I"
/codon_start=1
/product="proteasome subunit beta type-2 isoform 1"
/protein_id="NP_002785.1"
/db_xref="GI:4506195"
/db_xref="CCDS:CCDS394.1"
/db_xref="GeneID:5690"
/db_xref="HGNC:9539"
/db_xref="HPRD:03708"
/db_xref="MIM:602175"
/translation="
MEYLIGIQGPDYVLVASDRVAASNIVQMKDDHDKMFKMSEKILLLCVGEAGDTVQFAEYIQKNVQLYKMRNGYELSPTAAANFTRRNLADCLRSRTPYHVNLLLAGYDEHEGPALYYMDYLAALAKAPFAAHGYGAFLTLSILDRYYTPTISRERAVELLRKCLEELQKRFILNLPTFSVRIIDKNGIHDLDNISFPKQGS
"
misc_feature 413..988
/gene="PSMB2"
/gene_synonym="HC7-I"
/note="proteasome beta type-2 subunit. The 20S proteasome,
multisubunit proteolytic complex, is the central enzyme of
nonlysosomal protein degradation in both the cytosol and
nucleus. It is composed of 28 subunits arranged as four
homoheptameric rings that...; Region:
proteasome_beta_type_2; cd03758"
/db_xref="CDD:239727"
misc_feature 425..1006
/gene="PSMB2"
/gene_synonym="HC7-I"
/note="20S proteasome, alpha and beta subunits
[Posttranslational modification, protein turnover,
chaperones]; Region: PRE1; COG0638"
/db_xref="CDD:223711"
variation 449
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="g"
/replace="t"
/db_xref="dbSNP:11550444"
exon 504..626
/gene="PSMB2"
/gene_synonym="HC7-I"
/inference="alignment:Splign:1.39.8"
variation 526
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="g"
/replace="t"
/db_xref="dbSNP:11550446"
variation 545
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:59158931"
variation 557
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="g"
/replace="t"
/db_xref="dbSNP:1804238"
variation 595
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:11550443"
variation 603
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:11550447"
exon 627..697
/gene="PSMB2"
/gene_synonym="HC7-I"
/inference="alignment:Splign:1.39.8"
exon 698..860
/gene="PSMB2"
/gene_synonym="HC7-I"
/inference="alignment:Splign:1.39.8"
exon 861..910
/gene="PSMB2"
/gene_synonym="HC7-I"
/inference="alignment:Splign:1.39.8"
variation 887
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:1804236"
exon 911..4744
/gene="PSMB2"
/gene_synonym="HC7-I"
/inference="alignment:Splign:1.39.8"
variation 972
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="g"
/replace="t"
/db_xref="dbSNP:1804237"
STS 1017..1118
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="SHGC-35307"
/db_xref="UniSTS:2779"
variation 1023
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:12386"
variation 1053
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:60768546"
variation 1095
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:61192957"
variation 1170
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:61038979"
STS 1512..1614
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="D11S3114"
/db_xref="UniSTS:152207"
STS 1596..3115
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
STS 1596..1684
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="D8S2279"
/db_xref="UniSTS:473907"
STS 1615..3195
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="AB049870"
/db_xref="UniSTS:480103"
STS 1615..3156
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="D10S275"
/db_xref="UniSTS:147992"
STS 2041..2171
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="D15S1390"
/db_xref="UniSTS:474340"
variation 2102
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:1132065"
variation 2126
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:1132067"
variation 2137
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="a"
/replace="g"
/db_xref="dbSNP:1132068"
STS 2979..3154
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="D1S1425"
/db_xref="UniSTS:149621"
STS 2981..3151
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="G35510"
/db_xref="UniSTS:44150"
STS 3887..4030
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="SHGC-74572"
/db_xref="UniSTS:30275"
STS 4592..4696
/gene="PSMB2"
/gene_synonym="HC7-I"
/standard_name="SHGC-74576"
/db_xref="UniSTS:54319"
variation 4603
/gene="PSMB2"
/gene_synonym="HC7-I"
/replace="c"
/replace="t"
/db_xref="dbSNP:1062255"
polyA_site 4744
/gene="PSMB2"
/gene_synonym="HC7-I"
ORIGIN
ggggagattttaccgagcaacgtagggaaacggctgcctggctacctacccctttttgacacccacacgtgctcggcaccttacatacactgcgtgattttatcctaaagccacttttaaaatcttagtgtgtaaacagagaaactgggcgtcacataaggcaagtgacctgcacagcctgctccggaggagacccgtacgatcccagagacaagcactgaacataaggcacccggcgccgcgcccgctttgcaacctctcgcgacagttgtacgtcatccgagagcgccgtggaagtcgtgctgcaggcgtcgcgccaatcttcgctctgaggtgctgtctcaccggtgagacctggaagcgggcgagtctcgtgctgtgtcggacctgcagcccctggccttccgccaccatggagtacctcatcggtatccaaggccccgactatgttcttgtcgcctccgaccgggtggccgccagcaatattgtccagatgaaggacgatcatgacaagatgtttaagatgagtgaaaagatattactcctgtgtgttggagaggctggagacactgtacagtttgcagaatatattcagaaaaacgtgcaactttataagatgcgaaatggatatgaattgtctcccacggcagcagctaacttcacacgccgaaacctggctgactgtcttcggagtcggaccccatatcatgtgaacctcctcctggctggctatgatgagcatgaagggccagcgctgtattacatggactacctggcagccttggccaaggccccttttgcagcccacggctatggtgccttcctgactctcagtatcctcgaccgatactacacaccgactatctcacgtgagagggcagtggaactccttaggaaatgtctggaggagctccagaaacgcttcatcctgaatctgccaaccttcagtgttcgaatcattgacaaaaatggcatccatgacctggataacatttccttccccaaacagggctcctaacatcatgtcctccctcccacttgccagggaacttttttttgatgggctcctttatttttttctactcttttcaggcgcactcttgataaatggttaattcagaataaaggtgactatggatataattgagccctctggtccaggtctcagtttacctaatattacctcagaaaggatatggagggaagatgatctttttgccaggtctgacttttcttcctgctccgccctccattaacgctcagtaccctttagcagctgacggccccacgttctactccatgcttggcttcctttccaactagctctttcatatattttacttgctagtatctccattctctctaaagtagtggttctttttgcccttaaacttaaatttttaaattaattaacctgaattaataatacatgcacttaatgtaacatgcaaacagtacaaaaacatgtagtgaaaaatatttcttccagagctgggtgtggtggctcatacctgtaatcccagcactttgggaggccgaggcgggcggatcacgaggtcaagagagcgagaccatcctgaccaacatggtaaaaccccgtctctactaaaaatacaaaaattagctgggcgtggtggcacgcacccctagtcccagctactggggaggctgagacaggagaatcggtcgaacccgggaggcagaggttgcagtgagcctagatcgcgccactgtactccagcctggcaacagagtgagactccgtctcaaaaaaagaaggaaaaatgtttcttccatccctataatccagtcatctgcttcctgcttcccttcctggaggaaacttcagctactaatttcttatgttttttaagagatattctgttactgtgtaaagtatacatacatacagacacatgccccctttaaattttttagatttatttatttatttagagacagggtctcactctagcccaggctggagtgctgtggcgtaatcttggctcactgcaacctccgcctcccgggcccaagtgatcctcccatctcagcctcctgagtagctaggattacaggcgcacaccaccaatgcccagctagtttttgtgtttttcatagagacagggtctcaccatgtcattcaggttggtcttgaactcctgggctcaagcagtctgcctgccttggcttcccagtgctgggattacaggcgtgagccaccgtgcccggctaaaaagtatttttaagttctgcatattgcttatttcacttaacactatattagagattgttttatatcaatacatatagatatgcttattcttgttgacagttgcataattttccattaaattgatgtatcatgggcagttaaccagttactcgttttactcttagcataactttagggaacaatgtggatgttttgtggttaaagctattaaaacagtggttcttgaccagatgtgtgtttcagaatgttcatctcacatttccagttgctactgatgctgctggtctaggaaccacatatcaaaaccatttggtctccgactaagataaaccctactttatccaattctgtgctcctcttaatatcatatacagataggtttttgttttgtctgtgattaaatgtatcatctaagatactacctactgatcataacgttcatattaaagtattgggttaacattagatttgggtgtcttatacactatttaatacgccaatgataaatgccttacaccataagaagaaagctaatcattgagtaaatgggagaaaagagatgattcacgtcactacagttgattcaacctccaacaccaccatgaatatgcataggtttgagcttttagctagattcctgagtgtaaggcatctattttaaaagtgccacaggttggccgggtgcggtggctcatgcctgtaatcccagcactttggccgcccgccgaggcgggcggatcacctgaggtcaggagttcaagaccagcctggccaacatggtgaaaccccatctctactaaaaaaatatataacaattagccaggcgtggtggcacacgcctgtaaacccaactacttgggaggctgaggcaggagaattgcttgagcccgggagagggaggttgcagtgagccgagatcatgccactgcactccagcctggctgacagagcaagactctgtctcaaaaaaaaaaaaaaaaaaaaaaaaaaagcgccacagatgattctgacgccctacccagtggagtgctgctactaaagcacagactatcctgctacatgattttcccatctgtacaatgactgaaatagcacctattctatgtggtagatatgagaattccatgaagtaatataggtaaacatttagttcagggcttggcatgtggtaagtgctcagtaagtgtataatgattggtaaacttgttattctgcattcaggcctcaccagggatgacatacggttctctgcctttgaatgtaagtgtccccagggcaatctcaggcaagcctgcaaacccatcctgactctcagtgtttttttgccaatctggatctctttcctgagctccaaatcaactcattcctagatagctcaccctccagatttagggacatcgaactcagtatgtctaaagctgagccttaccatctgcccctctccaaaccgcctctatgacattctgtcttagagaattagagctacctggtttcccaagtgcccaagtcagaaacccaggcatcatttatttttaataaatgttttattttggaataaatttggttttacagaaaagttgcaaagataatatggtgtccttataccccttattcagtttctgtaatgttaacatcttctatataccacagtatgtttgtcaaaactgagaaaccaacattggttggtgtattagtattactaagctccaggctttattcagattttaccagtttttccactaattttcttctgttctaggatataatccaagatacaacattgcatttagctgggcatcatttttatgccattctttatctcctgtctctacatggccaccaagttctggcatttctacatcctaaatcttttaattttattataattttttattgttgtttttcagagacagggtcttgctccatcacctaggctggagtacagtggcacgatcgtagcttactgcagtaagttcacttgaactcctgggctcaagtgaacctcttaccccagcctcccaactagctgggactagaggggtgcaccactgcacccagctaattttgtcaaaattttttgtagagacagggtctcgccatgttgcctaggctggtctcgaactcttggcctcaagtgatcctcccaccttggtctgccaaagcactgggattacagatgtgagccactgcacccagcctaatctttataaatctccatccccattactctggttcaccccctatcgtttcttagactatttaacagcctcctaacttcactctacttttaatctcttccctctccaggtctttctccatattttaaaaaactagtttcaccatccattcctctctgcccttaaaactttctggtggttttccatggcttaagagaataaagcccaattctttgatttgacatgctaggcattccataatcctctccgaacctaactccccacttcctttccctcctttacacctcataaagcctgtgttccaactaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:5690 -> Molecular function: GO:0004298 [threonine-type endopeptidase activity] evidence: IEA
GeneID:5690 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
GeneID:5690 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS
GeneID:5690 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
GeneID:5690 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS
GeneID:5690 -> Biological process: GO:0002479 [antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent] evidence: TAS
GeneID:5690 -> Biological process: GO:0006521 [regulation of cellular amino acid metabolic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0006977 [DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest] evidence: TAS
GeneID:5690 -> Biological process: GO:0010243 [response to organonitrogen compound] evidence: IEA
GeneID:5690 -> Biological process: GO:0010467 [gene expression] evidence: TAS
GeneID:5690 -> Biological process: GO:0014070 [response to organic cyclic compound] evidence: IEA
GeneID:5690 -> Biological process: GO:0016032 [viral process] evidence: TAS
GeneID:5690 -> Biological process: GO:0016070 [RNA metabolic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0016071 [mRNA metabolic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA
GeneID:5690 -> Biological process: GO:0031145 [anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0034641 [cellular nitrogen compound metabolic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0042590 [antigen processing and presentation of exogenous peptide antigen via MHC class I] evidence: TAS
GeneID:5690 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
GeneID:5690 -> Biological process: GO:0051436 [negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
GeneID:5690 -> Biological process: GO:0051437 [positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
GeneID:5690 -> Biological process: GO:0051439 [regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
GeneID:5690 -> Cellular component: GO:0000502 [proteasome complex] evidence: TAS
GeneID:5690 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:5690 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
GeneID:5690 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
GeneID:5690 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:5690 -> Cellular component: GO:0005839 [proteasome core complex] evidence: ISS
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_002785 -> EC 3.4.25.1
by
@meso_cacase at
DBCLS
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