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2024-04-19 08:43:16, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_002796                925 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens proteasome (prosome, macropain) subunit, beta type, 4
            (PSMB4), mRNA.
ACCESSION   NM_002796
VERSION     NM_002796.2  GI:22538466
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 925)
  AUTHORS   Lee,K.M., Lee,J. and Park,C.S.
  TITLE     Cereblon inhibits proteasome activity by binding to the 20S core
            proteasome subunit beta type 4
  JOURNAL   Biochem. Biophys. Res. Commun. 427 (3), 618-622 (2012)
   PUBMED   23026050
  REMARK    GeneRIF: proteasome subunit beta type 4 (PSMB4), the beta7 subunit
            of the 20S core complex, was identified as a direct binding partner
            of CRBN.
REFERENCE   2  (bases 1 to 925)
  AUTHORS   Um,J.W., Im,E., Lee,H.J., Min,B., Yoo,L., Yoo,J., Lubbert,H.,
            Stichel-Gunkel,C., Cho,H.S., Yoon,J.B. and Chung,K.C.
  TITLE     Parkin directly modulates 26S proteasome activity
  JOURNAL   J. Neurosci. 30 (35), 11805-11814 (2010)
   PUBMED   20810900
  REMARK    GeneRIF: While 26 proteasome dysfunction is observed in Parkinson's
            disease (PD), diverse mutations in the parkin gene are linked to
            early-onset autosomal-recessive forms of familial PD.
REFERENCE   3  (bases 1 to 925)
  AUTHORS   Yoshida,T., Kato,K., Yokoi,K., Oguri,M., Watanabe,S., Metoki,N.,
            Yoshida,H., Satoh,K., Aoyagi,Y., Nozawa,Y. and Yamada,Y.
  TITLE     Association of genetic variants with hemorrhagic stroke in Japanese
            individuals
  JOURNAL   Int. J. Mol. Med. 25 (4), 649-656 (2010)
   PUBMED   20198315
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 925)
  AUTHORS   Oguri,M., Kato,K., Yokoi,K., Yoshida,T., Watanabe,S., Metoki,N.,
            Yoshida,H., Satoh,K., Aoyagi,Y., Nozawa,Y. and Yamada,Y.
  TITLE     Assessment of a polymorphism of SDK1 with hypertension in Japanese
            Individuals
  JOURNAL   Am. J. Hypertens. 23 (1), 70-77 (2010)
   PUBMED   19851296
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 925)
  AUTHORS   Wong,M.L., Dong,C., Maestre-Mesa,J. and Licinio,J.
  TITLE     Polymorphisms in inflammation-related genes are associated with
            susceptibility to major depression and antidepressant response
  JOURNAL   Mol. Psychiatry 13 (8), 800-812 (2008)
   PUBMED   18504423
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 925)
  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   7  (bases 1 to 925)
  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   8  (bases 1 to 925)
  AUTHORS   Gerards,W.L., Hop,F.W., Hendriks,I.L. and Bloemendal,H.
  TITLE     Cloning and expression of a human pro(tea)some beta-subunit cDNA: a
            homologue of the yeast PRE4-subunit essential for
            peptidylglutamyl-peptide hydrolase activity
  JOURNAL   FEBS Lett. 346 (2-3), 151-155 (1994)
   PUBMED   8013624
REFERENCE   9  (bases 1 to 925)
  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 925)
  AUTHORS   Lee,L.W., Moomaw,C.R., Orth,K., McGuire,M.J., DeMartino,G.N. and
            Slaughter,C.A.
  TITLE     Relationships among the subunits of the high molecular weight
            proteinase, macropain (proteasome)
  JOURNAL   Biochim. Biophys. Acta 1037 (2), 178-185 (1990)
   PUBMED   2306472
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from D26600.1.
            On Aug 29, 2002 this sequence version replaced gi:4506198.
            
            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. [provided by RefSeq, Jul
            2008].
            
            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 :: D26600.1, BQ057201.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
FEATURES             Location/Qualifiers
     source          1..925
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1q21"
     gene            1..925
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /note="proteasome (prosome, macropain) subunit, beta type,
                     4"
                     /db_xref="GeneID:5692"
                     /db_xref="HGNC:9541"
                     /db_xref="HPRD:03710"
                     /db_xref="MIM:602177"
     exon            1..163
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       7
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2296840"
     variation       15
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200946642"
     CDS             24..818
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /EC_number="3.4.25.1"
                     /note="proteasome subunit HsN3; proteasome beta chain;
                     macropain beta chain; proteasome chain 3; multicatalytic
                     endopeptidase complex beta chain; proteasome subunit, beta
                     type, 4; hsBPROS26; 26 kDa prosomal protein"
                     /codon_start=1
                     /product="proteasome subunit beta type-4"
                     /protein_id="NP_002787.2"
                     /db_xref="GI:22538467"
                     /db_xref="CCDS:CCDS996.1"
                     /db_xref="GeneID:5692"
                     /db_xref="HGNC:9541"
                     /db_xref="HPRD:03710"
                     /db_xref="MIM:602177"
                     /translation="
MEAFLGSRSGLWAGGPAPGQFYRIPSTPDSFMDPASALYRGPITRTQNPMVTGTSVLGVKFEGGVVIAADMLGSYGSLARFRNISRIMRVNNSTMLGASGDYADFQYLKQVLGQMVIDEELLGDGHSYSPRAIHSWLTRAMYSRRSKMNPLWNTMVIGGYADGESFLGYVDMLGVAYEAPSLATGYGAYLAQPLLREVLEKQPVLSQTEARDLVERCMRVLYYRDARSYNRFQIATVTEKGVEIEGPLSTETNWDIAHMISGFE
"
     misc_feature    156..746
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /note="20S proteasome, alpha and beta subunits
                     [Posttranslational modification, protein turnover,
                     chaperones]; Region: PRE1; COG0638"
                     /db_xref="CDD:30983"
     misc_feature    177..764
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /note="proteasome beta type-4 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_4; cd03760"
                     /db_xref="CDD:48458"
     misc_feature    order(183..185,231..233,237..239,279..281,579..581,
                     696..698,705..710)
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /note="active site"
                     /db_xref="CDD:48458"
     misc_feature    order(237..239,246..248,252..269,327..329,333..335,
                     378..380,417..419,426..431,435..440,447..449,456..458,
                     534..536,540..542,546..557,564..566,588..593,597..602,
                     609..617,669..671,690..701,708..713)
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /note="beta subunit interaction site [polypeptide
                     binding]; other site"
                     /db_xref="CDD:48458"
     misc_feature    327..329
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphotyrosine; propagated from
                     UniProtKB/Swiss-Prot (P28070.4); phosphorylation site"
     misc_feature    327..329
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     variation       25
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199968815"
     variation       31
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372329683"
     variation       41
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188568243"
     variation       45
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11557384"
     variation       51
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11557386"
     variation       62
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:149809535"
     variation       66
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111502283"
     STS             75..543
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /standard_name="stSG627163"
                     /db_xref="UniSTS:457256"
     variation       91
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115066321"
     variation       98
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7172"
     variation       144
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375090204"
     variation       145
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113331137"
     exon            164..370
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       224
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371543427"
     variation       233
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11557388"
     variation       246
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:199924460"
     variation       271
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373620750"
     STS             285..558
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /standard_name="MARC_13789-13790:1025290513:1"
                     /db_xref="UniSTS:267555"
     variation       296
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115195104"
     variation       308
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1804241"
     variation       312
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11557387"
     variation       323
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:6684391"
     variation       359
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11557389"
     variation       360
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372581320"
     exon            371..517
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       371
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145190029"
     variation       447
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201438006"
     variation       453
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367717074"
     variation       454
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140771260"
     variation       468
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:3209764"
     variation       473
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:14276"
     variation       482
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:114882311"
     variation       489
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371316814"
     variation       511
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3209765"
     exon            518..599
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       565
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11557382"
     variation       566
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1804239"
     variation       580
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11557385"
     variation       589
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:17407993"
     variation       593
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3209715"
     exon            600..716
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       609
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372714296"
     variation       648
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:202077271"
     variation       650
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146990256"
     variation       675
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115063024"
     variation       677
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200407470"
     variation       679
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143739858"
     STS             687..800
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /standard_name="G54029"
                     /db_xref="UniSTS:109411"
     STS             687..764
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /standard_name="REN33989"
                     /db_xref="UniSTS:358789"
     variation       695
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201140984"
     variation       702
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148730084"
     STS             714..794
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /standard_name="RH64651"
                     /db_xref="UniSTS:35030"
     exon            717..805
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       724
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4603"
     variation       726
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144372831"
     variation       728
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116353887"
     variation       732
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369317780"
     variation       738
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144890599"
     variation       744
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374028323"
     variation       790
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142070497"
     exon            806..925
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /inference="alignment:Splign:1.39.8"
     variation       823
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370398473"
     variation       841
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1804240"
     variation       850
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373812658"
     polyA_signal    908..913
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
     polyA_site      925
                     /gene="PSMB4"
                     /gene_synonym="HN3; HsN3; PROS-26; PROS26"
                     /experiment="experimental evidence, no additional details
                     recorded"
ORIGIN      
ttttttctgctaccgtgactaagatggaagcgtttttggggtcgcggtccggactttgggcggggggtccggccccaggacagttttaccgcattccgtccactcccgattccttcatggatccggcgtctgcactttacagaggtccaatcacgcggacccagaaccccatggtgaccgggacctcagtcctcggcgttaagttcgagggcggagtggtgattgccgcagacatgctgggatcctacggctccttggctcgtttccgcaacatctctcgcattatgcgagtcaacaacagtaccatgctgggtgcctctggcgactacgctgatttccagtatttgaagcaagttctcggccagatggtgattgatgaggagcttctgggagatggacacagctatagtcctagagctattcattcatggctgaccagggccatgtacagccggcgctcgaagatgaaccctttgtggaacaccatggtcatcggaggctatgctgatggagagagcttcctcggttatgtggacatgcttggtgtagcctatgaagccccttcgctggccactggttatggtgcatacttggctcagcctctgctgcgagaagttctggagaagcagccagtgctaagccagaccgaggcccgcgacttagtagaacgctgcatgcgagtgctgtactaccgagatgcccgttcttacaaccggtttcaaatcgccactgtcaccgaaaaaggtgttgaaatagagggaccattgtctacagagaccaactgggatattgcccacatgatcagtggctttgaatgaaatacagatgcattatccagaactgaagttgccctacttttaactttgaacttggctagttcaaagatagactcttcttttgtaaagtaaataaattcttcaaaatg
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5692 -> Molecular function: GO:0001530 [lipopolysaccharide binding] evidence: IEA
            GeneID:5692 -> Molecular function: GO:0004298 [threonine-type endopeptidase activity] evidence: IEA
            GeneID:5692 -> Biological process: GO:0000082 [G1/S transition of mitotic cell cycle] evidence: TAS
            GeneID:5692 -> Biological process: GO:0000209 [protein polyubiquitination] evidence: TAS
            GeneID:5692 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
            GeneID:5692 -> Biological process: GO:0002474 [antigen processing and presentation of peptide antigen via MHC class I] evidence: TAS
            GeneID:5692 -> Biological process: GO:0002479 [antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent] evidence: TAS
            GeneID:5692 -> Biological process: GO:0002862 [negative regulation of inflammatory response to antigenic stimulus] evidence: IEA
            GeneID:5692 -> Biological process: GO:0006521 [regulation of cellular amino acid metabolic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0006915 [apoptotic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0006977 [DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest] evidence: TAS
            GeneID:5692 -> Biological process: GO:0010467 [gene expression] evidence: TAS
            GeneID:5692 -> Biological process: GO:0016032 [viral process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0016070 [RNA metabolic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0016071 [mRNA metabolic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0019048 [modulation by virus of host morphology or physiology] evidence: IEA
            GeneID:5692 -> Biological process: GO:0031145 [anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0034641 [cellular nitrogen compound metabolic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0042590 [antigen processing and presentation of exogenous peptide antigen via MHC class I] evidence: TAS
            GeneID:5692 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS
            GeneID:5692 -> Biological process: GO:0051436 [negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5692 -> Biological process: GO:0051437 [positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5692 -> Biological process: GO:0051439 [regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle] evidence: TAS
            GeneID:5692 -> Cellular component: GO:0000502 [proteasome complex] evidence: TAS
            GeneID:5692 -> Cellular component: GO:0005634 [nucleus] evidence: TAS
            GeneID:5692 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
            GeneID:5692 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:5692 -> Cellular component: GO:0005839 [proteasome core complex] evidence: ISS
ANNOTATIONS from NCBI Entrez Gene (20130726):
            NP_002787 -> EC 3.4.25.1

by @meso_cacase at DBCLS
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