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2024-04-27 09:08:44, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_002788               1014 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens proteasome (prosome, macropain) subunit, alpha type, 3
            (PSMA3), transcript variant 1, mRNA.
ACCESSION   NM_002788
VERSION     NM_002788.3  GI:330688466
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 1014)
  AUTHORS   Fedorova,O.A., Moiseeva,T.N., Nikiforov,A.A., Tsimokha,A.S.,
            Livinskaya,V.A., Hodson,M., Bottrill,A., Evteeva,I.N.,
            Ermolayeva,J.B., Kuznetzova,I.M., Turoverov,K.K., Eperon,I. and
            Barlev,N.A.
  TITLE     Proteomic analysis of the 20S proteasome (PSMA3)-interacting
            proteins reveals a functional link between the proteasome and mRNA
            metabolism
  JOURNAL   Biochem. Biophys. Res. Commun. 416 (3-4), 258-265 (2011)
   PUBMED   22079093
  REMARK    GeneRIF: A combination of two-dimensional gel electrophoresis
            (2D-GE) and tandem mass-spectrometry revealed a large number of
            PSMA3-bound proteins that are involved in various aspects of mRNA
            metabolism, including splicing.
REFERENCE   2  (bases 1 to 1014)
  AUTHORS   Boncela,J., Przygodzka,P., Papiewska-Pajak,I., Wyroba,E.,
            Osinska,M. and Cierniewski,C.S.
  TITLE     Plasminogen activator inhibitor type 1 interacts with alpha3
            subunit of proteasome and modulates its activity
  JOURNAL   J. Biol. Chem. 286 (8), 6820-6831 (2011)
   PUBMED   21135093
  REMARK    GeneRIF: Plasminogen activator inhibitor type 1 interacts with
            alpha3 subunit of proteasome and modulates its activity.
REFERENCE   3  (bases 1 to 1014)
  AUTHORS   Yousef,A.A., Suliman,G.A. and Mabrouk,M.M.
  TITLE     The value of correlation of serum 20S proteasome concentration and
            percentage of lymphocytic apoptosis in critically ill patients: a
            prospective observational study
  JOURNAL   Crit Care 14 (6), R215 (2010)
   PUBMED   21108816
  REMARK    GeneRIF: Serum 20S proteasome concentration and percentage of
            lymphocytic apoptosis predicted survival and patient prognosis in
            critically ill patients.
REFERENCE   4  (bases 1 to 1014)
  AUTHORS   Parfitt,D.A., Michael,G.J., Vermeulen,E.G., Prodromou,N.V.,
            Webb,T.R., Gallo,J.M., Cheetham,M.E., Nicoll,W.S., Blatch,G.L. and
            Chapple,J.P.
  TITLE     The ataxia protein sacsin is a functional co-chaperone that
            protects against polyglutamine-expanded ataxin-1
  JOURNAL   Hum. Mol. Genet. 18 (9), 1556-1565 (2009)
   PUBMED   19208651
REFERENCE   5  (bases 1 to 1014)
  AUTHORS   Yuksek,K., Chen,W.L., Chien,D. and Ou,J.H.
  TITLE     Ubiquitin-independent degradation of hepatitis C virus F protein
  JOURNAL   J. Virol. 83 (2), 612-621 (2009)
   PUBMED   18971267
  REMARK    GeneRIF: The authors propose that the full-length HCV F protein as
            well as the F protein initiating from codon 26 is degraded by an
            ubiquitin-independent pathway that is mediated by the proteasome
            subunit alpha3.
REFERENCE   6  (bases 1 to 1014)
  AUTHORS   Castano,J.G., Mahillo,E., Arizti,P. and Arribas,J.
  TITLE     Phosphorylation of C8 and C9 subunits of the multicatalytic
            proteinase by casein kinase II and identification of the C8
            phosphorylation sites by direct mutagenesis
  JOURNAL   Biochemistry 35 (12), 3782-3789 (1996)
   PUBMED   8619999
REFERENCE   7  (bases 1 to 1014)
  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   8  (bases 1 to 1014)
  AUTHORS   Akioka,H., Forsberg,N.E., Ishida,N., Okumura,K., Nogami,M.,
            Taguchi,H., Noda,C. and Tanaka,K.
  TITLE     Isolation and characterization of the HC8 subunit gene of the human
            proteasome
  JOURNAL   Biochem. Biophys. Res. Commun. 207 (1), 318-323 (1995)
   PUBMED   7857283
REFERENCE   9  (bases 1 to 1014)
  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   10 (bases 1 to 1014)
  AUTHORS   Tamura,T., Lee,D.H., Osaka,F., Fujiwara,T., Shin,S., Chung,C.H.,
            Tanaka,K. and Ichihara,A.
  TITLE     Molecular cloning and sequence analysis of cDNAs for five major
            subunits of human proteasomes (multi-catalytic proteinase
            complexes)
  JOURNAL   Biochim. Biophys. Acta 1089 (1), 95-102 (1991)
   PUBMED   2025653
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from CF128376.1, D00762.1 and
            BC038990.1.
            On Apr 27, 2011 this sequence version replaced gi:23110937.
            
            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 peptidase T1A family, that is a 20S core alpha
            subunit. Two alternative transcripts encoding different isoforms
            have been identified. [provided by RefSeq, Jul 2008].
            
            Transcript Variant: This variant (1) encodes the longer isoform.
            
            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 :: BC038990.1, BQ955290.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-111               CF128376.1         1-111
            112-949             D00762.1           1-838
            950-1014            BC038990.1         877-941
FEATURES             Location/Qualifiers
     source          1..1014
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="14"
                     /map="14q23"
     gene            1..1014
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /note="proteasome (prosome, macropain) subunit, alpha
                     type, 3"
                     /db_xref="GeneID:5684"
                     /db_xref="HGNC:9532"
                     /db_xref="HPRD:01463"
                     /db_xref="MIM:176843"
     exon            1..137
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    63..65
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /note="upstream in-frame stop codon"
     variation       72
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200319799"
     variation       76
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:375729415"
     variation       79
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200837709"
     variation       80
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201941830"
     variation       83
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371805393"
     variation       89
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187984170"
     CDS             117..884
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /EC_number="3.4.25.1"
                     /note="isoform 1 is encoded by transcript variant 1;
                     proteasome subunit C8; macropain subunit C8;
                     multicatalytic endopeptidase complex subunit C8;
                     proteasome subunit alpha type-3; proteasome component C8"
                     /codon_start=1
                     /product="proteasome subunit alpha type-3 isoform 1"
                     /protein_id="NP_002779.1"
                     /db_xref="GI:4506183"
                     /db_xref="CCDS:CCDS9731.1"
                     /db_xref="GeneID:5684"
                     /db_xref="HGNC:9532"
                     /db_xref="HPRD:01463"
                     /db_xref="MIM:176843"
                     /translation="
MSSIGTGYDLSASTFSPDGRVFQVEYAMKAVENSSTAIGIRCKDGVVFGVEKLVLSKLYEEGSNKRLFNVDRHVGMAVAGLLADARSLADIAREEASNFRSNFGYNIPLKHLADRVAMYVHAYTLYSAVRPFGCSFMLGSYSVNDGAQLYMIDPSGVSYGYWGCAIGKARQAAKTEIEKLQMKEMTCRDIVKEVAKIIYIVHDEVKDKAFELELSWVGELTNGRHEIVPKDIREEAEKYAKESLKEEDESDDDNM
"
     misc_feature    120..122
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N-acetylserine; propagated from
                     UniProtKB/Swiss-Prot (P25788.2); acetylation site"
     misc_feature    120..122
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="acetylation site"
     misc_feature    129..767
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /note="proteasome_alpha_type_3. 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 stack on...; Region:
                     proteasome_alpha_type_3; cd03751"
                     /db_xref="CDD:48449"
     misc_feature    132..833
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /note="proteasome subunit alpha; Provisional; Region:
                     PRK03996"
                     /db_xref="CDD:179701"
     misc_feature    order(144..155,159..164,168..173,183..185,192..194,
                     201..206,213..215,237..239,282..284,288..293,360..368,
                     372..377,468..470,477..479,486..491,498..512,564..566,
                     579..584,588..590,594..599,603..605)
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /note="alpha subunit interaction site [polypeptide
                     binding]; other site"
                     /db_xref="CDD:48449"
     misc_feature    order(219..221,267..269,273..275,312..314,618..620)
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /note="active site"
                     /db_xref="CDD:48449"
     misc_feature    285..287
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (P25788.2); acetylation site"
     misc_feature    597..599
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    732..734
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (P25788.2); acetylation site"
     misc_feature    804..806
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (P25788.2); acetylation site"
     misc_feature    843..845
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P25788.2); phosphorylation site"
     misc_feature    843..845
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
                     /citation=[6]
     misc_feature    843..845
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
                     /citation=[6]
                     /db_xref="HPRD:00277"
     misc_feature    864..866
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P25788.2); phosphorylation site"
     misc_feature    864..866
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    864..866
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     variation       131
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368712816"
     exon            138..220
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       191
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199770893"
     variation       197
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201912576"
     variation       215
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373005377"
     exon            221..344
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       254
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11556302"
     variation       260
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181507532"
     variation       263
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144084081"
     variation       314
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145114489"
     variation       315
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370015963"
     exon            345..446
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       383
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17852655"
     variation       389
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17852656"
     variation       390
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374139645"
     variation       392
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11556303"
     variation       397
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199944562"
     variation       431
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11556304"
     variation       434
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377189095"
     exon            447..520
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     exon            521..593
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       557
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374534971"
     variation       593
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112146406"
     exon            594..659
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       599
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149394834"
     variation       610
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144791534"
     variation       614
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189216032"
     variation       626
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17852654"
     exon            660..706
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       666
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377728633"
     variation       697
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148626478"
     variation       706
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142139987"
     exon            707..774
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       714
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200984115"
     variation       725
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146180750"
     variation       729
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373695669"
     variation       731
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376700376"
     variation       743
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:3208867"
     exon            775..839
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       783
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368886678"
     variation       806
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201086253"
     variation       820
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:139132472"
     STS             829..966
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /standard_name="RH17928"
                     /db_xref="UniSTS:51626"
     variation       834
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3208868"
     variation       835
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3208869"
     exon            840..998
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /inference="alignment:Splign:1.39.8"
     variation       842
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376830435"
     STS             845..969
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /standard_name="SHGC-32634"
                     /db_xref="UniSTS:21204"
     STS             850..969
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /standard_name="SHGC-34645"
                     /db_xref="UniSTS:21203"
     variation       857
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:144136958"
     variation       902
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369029493"
     variation       954..955
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:3830963"
     variation       968..969
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:34841681"
     polyA_signal    974..979
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
     polyA_site      998
                     /gene="PSMA3"
                     /gene_synonym="HC8; PSC3"
ORIGIN      
gttattggttggcagttcagccaatgagcgggcctgttactagtttgcggcatcctgtggtataggggaagcgctccgggcctggaatccctacgcgtccctttgggtttagcacgatgagctcaatcggcactgggtatgacctgtcagcctctacattctctcctgacggaagagtttttcaagttgaatatgctatgaaggctgtggaaaatagtagtacagctattggaatcagatgcaaagatggtgttgtctttggggtagaaaaattagtcctttctaaactttatgaagaaggttccaacaaaagactttttaatgttgatcggcatgttggaatggcagtagcaggtttgttggcagatgctcgttctttagcagacatagcaagagaagaagcttccaacttcagatctaactttggctacaacattccactaaaacatcttgcagacagagtggccatgtatgtgcatgcatatacactctacagtgctgttagaccttttggctgcagtttcatgttagggtcttacagtgtgaatgacggtgcgcaactctacatgattgacccatcaggtgtttcatacggttattggggctgtgccatcggcaaagccaggcaagctgcaaagacggaaatagagaagcttcagatgaaagaaatgacctgccgtgatatcgttaaagaagttgcaaaaataatttacatagtacatgacgaagttaaggataaagcttttgaactagaactcagctgggttggtgaattaactaatggaagacatgaaattgttccaaaagatataagagaagaagcagagaaatatgctaaggaatctctgaaggaagaagatgaatcagatgatgataatatgtaacatttactccagcatctattgtattttaaatttctactccagtccaatgtaactatttagccctggattatacatactgtccaattttcattaaatttttgtcttataactattaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5684 -> Molecular function: GO:0004298 [threonine-type endopeptidase activity] evidence: IEA
            GeneID:5684 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:5684 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
            GeneID:5684 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS
            GeneID:5684 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
            GeneID:5684 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS
            GeneID:5684 -> Biological process: GO:0002479 [antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent] evidence: TAS
            GeneID:5684 -> Biological process: GO:0006521 [regulation of cellular amino acid metabolic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0006977 [DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest] evidence: TAS
            GeneID:5684 -> Biological process: GO:0010467 [gene expression] evidence: TAS
            GeneID:5684 -> Biological process: GO:0016032 [viral process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0016070 [RNA metabolic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0016071 [mRNA metabolic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA
            GeneID:5684 -> Biological process: GO:0031145 [anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0034641 [cellular nitrogen compound metabolic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0042590 [antigen processing and presentation of exogenous peptide antigen via MHC class I] evidence: TAS
            GeneID:5684 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
            GeneID:5684 -> Biological process: GO:0051436 [negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5684 -> Biological process: GO:0051437 [positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5684 -> Biological process: GO:0051439 [regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5684 -> Cellular component: GO:0000502 [proteasome complex] evidence: TAS
            GeneID:5684 -> Cellular component: GO:0005634 [nucleus] evidence: TAS
            GeneID:5684 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
            GeneID:5684 -> Cellular component: GO:0005737 [cytoplasm] evidence: TAS
            GeneID:5684 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:5684 -> Cellular component: GO:0005839 [proteasome core complex] evidence: IDA
            GeneID:5684 -> Cellular component: GO:0019773 [proteasome core complex, alpha-subunit complex] evidence: IEA
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_002779 -> EC 3.4.25.1

by @meso_cacase at DBCLS
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