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WDR27_HUMAN
ID   WDR27_HUMAN             Reviewed;         827 AA.
AC   A2RRH5; A5PLM8; C9JGV0; Q5T066;
DT   02-OCT-2007, integrated into UniProtKB/Swiss-Prot.
DT   05-APR-2011, sequence version 3.
DT   03-AUG-2022, entry version 117.
DE   RecName: Full=WD repeat-containing protein 27;
GN   Name=WDR27;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=14574404; DOI=10.1038/nature02055;
RA   Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L.,
RA   Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E., Gilbert J.G.R.,
RA   Clamp M.E., Bethel G., Milne S., Ainscough R., Almeida J.P., Ambrose K.D.,
RA   Andrews T.D., Ashwell R.I.S., Babbage A.K., Bagguley C.L., Bailey J.,
RA   Banerjee R., Barker D.J., Barlow K.F., Bates K., Beare D.M., Beasley H.,
RA   Beasley O., Bird C.P., Blakey S.E., Bray-Allen S., Brook J., Brown A.J.,
RA   Brown J.Y., Burford D.C., Burrill W., Burton J., Carder C., Carter N.P.,
RA   Chapman J.C., Clark S.Y., Clark G., Clee C.M., Clegg S., Cobley V.,
RA   Collier R.E., Collins J.E., Colman L.K., Corby N.R., Coville G.J.,
RA   Culley K.M., Dhami P., Davies J., Dunn M., Earthrowl M.E., Ellington A.E.,
RA   Evans K.A., Faulkner L., Francis M.D., Frankish A., Frankland J.,
RA   French L., Garner P., Garnett J., Ghori M.J., Gilby L.M., Gillson C.J.,
RA   Glithero R.J., Grafham D.V., Grant M., Gribble S., Griffiths C.,
RA   Griffiths M.N.D., Hall R., Halls K.S., Hammond S., Harley J.L., Hart E.A.,
RA   Heath P.D., Heathcott R., Holmes S.J., Howden P.J., Howe K.L., Howell G.R.,
RA   Huckle E., Humphray S.J., Humphries M.D., Hunt A.R., Johnson C.M.,
RA   Joy A.A., Kay M., Keenan S.J., Kimberley A.M., King A., Laird G.K.,
RA   Langford C., Lawlor S., Leongamornlert D.A., Leversha M., Lloyd C.R.,
RA   Lloyd D.M., Loveland J.E., Lovell J., Martin S., Mashreghi-Mohammadi M.,
RA   Maslen G.L., Matthews L., McCann O.T., McLaren S.J., McLay K., McMurray A.,
RA   Moore M.J.F., Mullikin J.C., Niblett D., Nickerson T., Novik K.L.,
RA   Oliver K., Overton-Larty E.K., Parker A., Patel R., Pearce A.V., Peck A.I.,
RA   Phillimore B.J.C.T., Phillips S., Plumb R.W., Porter K.M., Ramsey Y.,
RA   Ranby S.A., Rice C.M., Ross M.T., Searle S.M., Sehra H.K., Sheridan E.,
RA   Skuce C.D., Smith S., Smith M., Spraggon L., Squares S.L., Steward C.A.,
RA   Sycamore N., Tamlyn-Hall G., Tester J., Theaker A.J., Thomas D.W.,
RA   Thorpe A., Tracey A., Tromans A., Tubby B., Wall M., Wallis J.M.,
RA   West A.P., White S.S., Whitehead S.L., Whittaker H., Wild A., Willey D.J.,
RA   Wilmer T.E., Wood J.M., Wray P.W., Wyatt J.C., Young L., Younger R.M.,
RA   Bentley D.R., Coulson A., Durbin R.M., Hubbard T., Sulston J.E., Dunham I.,
RA   Rogers J., Beck S.;
RT   "The DNA sequence and analysis of human chromosome 6.";
RL   Nature 425:805-811(2003).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 2; 3 AND 4), AND VARIANTS
RP   PRO-133 AND HIS-437.
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
CC   -!- INTERACTION:
CC       A2RRH5; P08243: ASNS; NbExp=3; IntAct=EBI-9476803, EBI-722989;
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=4;
CC       Name=1;
CC         IsoId=A2RRH5-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=A2RRH5-2; Sequence=VSP_028510;
CC       Name=3;
CC         IsoId=A2RRH5-3; Sequence=VSP_028511, VSP_028512;
CC       Name=4;
CC         IsoId=A2RRH5-4; Sequence=VSP_040796, VSP_040797;
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DR   EMBL; AL031315; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; AL135910; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; AL441927; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; AL513547; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; BC040606; -; NOT_ANNOTATED_CDS; mRNA.
DR   EMBL; BC131633; AAI31634.1; -; mRNA.
DR   EMBL; BC142982; AAI42983.1; -; mRNA.
DR   CCDS; CCDS47520.2; -. [A2RRH5-4]
DR   CCDS; CCDS56459.1; -. [A2RRH5-2]
DR   RefSeq; NP_001189479.1; NM_001202550.1. [A2RRH5-2]
DR   RefSeq; NP_872358.4; NM_182552.4. [A2RRH5-4]
DR   AlphaFoldDB; A2RRH5; -.
DR   BioGRID; 128986; 22.
DR   IntAct; A2RRH5; 2.
DR   STRING; 9606.ENSP00000416289; -.
DR   iPTMnet; A2RRH5; -.
DR   PhosphoSitePlus; A2RRH5; -.
DR   BioMuta; WDR27; -.
DR   MassIVE; A2RRH5; -.
DR   PaxDb; A2RRH5; -.
DR   PeptideAtlas; A2RRH5; -.
DR   PRIDE; A2RRH5; -.
DR   TopDownProteomics; A2RRH5-2; -. [A2RRH5-2]
DR   Antibodypedia; 49469; 105 antibodies from 18 providers.
DR   DNASU; 253769; -.
DR   Ensembl; ENST00000423258.5; ENSP00000397869.1; ENSG00000184465.16. [A2RRH5-2]
DR   Ensembl; ENST00000448612.6; ENSP00000416289.1; ENSG00000184465.16. [A2RRH5-4]
DR   GeneID; 253769; -.
DR   KEGG; hsa:253769; -.
DR   MANE-Select; ENST00000448612.6; ENSP00000416289.1; NM_182552.5; NP_872358.4. [A2RRH5-4]
DR   UCSC; uc003qwx.4; human. [A2RRH5-1]
DR   CTD; 253769; -.
DR   DisGeNET; 253769; -.
DR   GeneCards; WDR27; -.
DR   HGNC; HGNC:21248; WDR27.
DR   HPA; ENSG00000184465; Low tissue specificity.
DR   neXtProt; NX_A2RRH5; -.
DR   OpenTargets; ENSG00000184465; -.
DR   PharmGKB; PA134875091; -.
DR   VEuPathDB; HostDB:ENSG00000184465; -.
DR   eggNOG; KOG0266; Eukaryota.
DR   GeneTree; ENSGT00390000012017; -.
DR   HOGENOM; CLU_018295_0_0_1; -.
DR   InParanoid; A2RRH5; -.
DR   OMA; EFCPWQT; -.
DR   OrthoDB; 698548at2759; -.
DR   PhylomeDB; A2RRH5; -.
DR   TreeFam; TF351563; -.
DR   PathwayCommons; A2RRH5; -.
DR   SignaLink; A2RRH5; -.
DR   BioGRID-ORCS; 253769; 5 hits in 1082 CRISPR screens.
DR   ChiTaRS; WDR27; human.
DR   GenomeRNAi; 253769; -.
DR   Pharos; A2RRH5; Tdark.
DR   PRO; PR:A2RRH5; -.
DR   Proteomes; UP000005640; Chromosome 6.
DR   RNAct; A2RRH5; protein.
DR   Bgee; ENSG00000184465; Expressed in right uterine tube and 156 other tissues.
DR   ExpressionAtlas; A2RRH5; baseline and differential.
DR   Genevisible; A2RRH5; HS.
DR   GO; GO:0005654; C:nucleoplasm; IDA:HPA.
DR   Gene3D; 2.130.10.10; -; 3.
DR   InterPro; IPR011047; Quinoprotein_ADH-like_supfam.
DR   InterPro; IPR015943; WD40/YVTN_repeat-like_dom_sf.
DR   InterPro; IPR001680; WD40_repeat.
DR   InterPro; IPR042411; WDR27.
DR   PANTHER; PTHR44525; PTHR44525; 1.
DR   Pfam; PF00400; WD40; 5.
DR   SMART; SM00320; WD40; 10.
DR   SUPFAM; SSF50998; SSF50998; 1.
DR   PROSITE; PS50082; WD_REPEATS_2; 3.
DR   PROSITE; PS50294; WD_REPEATS_REGION; 2.
PE   1: Evidence at protein level;
KW   Alternative splicing; Reference proteome; Repeat; WD repeat.
FT   CHAIN           1..827
FT                   /note="WD repeat-containing protein 27"
FT                   /id="PRO_0000306831"
FT   REPEAT          3..57
FT                   /note="WD 1"
FT   REPEAT          62..101
FT                   /note="WD 2"
FT   REPEAT          112..151
FT                   /note="WD 3"
FT   REPEAT          155..194
FT                   /note="WD 4"
FT   REPEAT          201..237
FT                   /note="WD 5"
FT   REPEAT          292..337
FT                   /note="WD 6"
FT   REPEAT          344..387
FT                   /note="WD 7"
FT   REPEAT          502..542
FT                   /note="WD 8"
FT   REPEAT          546..584
FT                   /note="WD 9"
FT   REPEAT          590..629
FT                   /note="WD 10"
FT   REPEAT          646..687
FT                   /note="WD 11"
FT   REPEAT          698..740
FT                   /note="WD 12"
FT   REPEAT          746..784
FT                   /note="WD 13"
FT   REPEAT          788..826
FT                   /note="WD 14"
FT   VAR_SEQ         111..207
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_028510"
FT   VAR_SEQ         111..112
FT                   /note="GL -> GK (in isoform 3)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_028511"
FT   VAR_SEQ         113..827
FT                   /note="Missing (in isoform 3)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_028512"
FT   VAR_SEQ         152
FT                   /note="E -> EQRFSVTYIERPDVNNRHKVPPPTFLHTFSQ (in isoform 4)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_040796"
FT   VAR_SEQ         812..827
FT                   /note="LATATLDGKLQLFLAE -> MESRSVAHAGVQWHDLGSLQPPPSRFKQFFCL
FT                   SLPSSWDYSLPQLPWMVNSSSF (in isoform 4)"
FT                   /evidence="ECO:0000303|PubMed:15489334"
FT                   /id="VSP_040797"
FT   VARIANT         133
FT                   /note="L -> P (in dbSNP:rs4236176)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_035317"
FT   VARIANT         393
FT                   /note="V -> L (in dbSNP:rs35895089)"
FT                   /id="VAR_035318"
FT   VARIANT         437
FT                   /note="R -> H (in dbSNP:rs3800544)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_035319"
FT   VARIANT         470
FT                   /note="P -> L (in dbSNP:rs34313252)"
FT                   /id="VAR_035320"
FT   VARIANT         697
FT                   /note="A -> V (in dbSNP:rs9396946)"
FT                   /id="VAR_035321"
FT   CONFLICT        153
FT                   /note="T -> A (in Ref. 2; BC040606)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        512
FT                   /note="T -> S (in Ref. 2; AAI31634/AAI42983)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        A2RRH5-4:845
FT                   /note="R -> C (in Ref. 2; BC040606)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        A2RRH5-4:875
FT                   /note="L -> F (in Ref. 2; BC040606)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   827 AA;  90038 MW;  932404623943AC4C CRC64;
     MENPQDIFSS NGGCLSDIVI EKYLVESKES VSHVQLACSM QDCAFPLDGT ELCIWNTKDP
     SHQLLILRGH HQPITAMAFG NKVNPLLICS ASLDYVIMWN LDECREKVLQ GLVPRGTVMG
     SLLGKVLCLQ LSLDDHVVAV CAGNKIFMLD IETQAVRAEL QGHLGPVTAV EFCPWRAGTL
     ISASEDRGFK VWDHCTGSLI YSSSVLSAYP LLSLFIDAES RQLVTGCADG QLWIFSLMDG
     HHYRRVARVD LRKKTETFST RRVKSGLCSQ PEESQLPSTS ALGKGEQVEV TFPVLRLAPC
     DLSLIPNSAC GCLSSENTRC VWIGSSVGLF VFNLANLEVE AALYYKDFQS LSILLAGSCA
     LRNRTADQKV LCLLASLFGG KIAVLEINPA ALVRAQQCPS MGQSLSVPAS SCVLPTSPLY
     LGIAKEKSTK AASEQRRAAR NVMKDQRLVF HSKVRSSGYA SAPHVTMFSP KTNIKSEGKG
     SSRSRSSCAR EAYPVECAVP TKPGPQVAAA PTCTRVCCIQ YSGDGQWLAC GLANHLLLVF
     DASLTGTPAV FSGHDGAVNA VCWSQDRRWL LSAARDGTLR MWSARGAELA LLLGKDMFSK
     PIQSAQFYYI DAFILLSSGP EFQLLRYHID TCKDEIKRYK QKSKSKLICR LSTTGAVDMT
     SLSAVNDFYS HIVLAAGRNR TVEVFDLNAG CSAAVIAEAH SRPVHQICQN KGSSFTTQQP
     QAYNLFLTTA IGDGMRLWDL RTLRCERHFE GHPTRGYPCG IAFSPCGRFA ACGAEDRHAY
     VYEMGSSTFS HRLAGHTDTV TGVAFNPSAP QLATATLDGK LQLFLAE
 
 
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