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GDPD4_HUMAN
ID   GDPD4_HUMAN             Reviewed;         623 AA.
AC   Q6W3E5; Q7Z5B0;
DT   03-OCT-2006, integrated into UniProtKB/Swiss-Prot.
DT   05-JUL-2004, sequence version 1.
DT   03-AUG-2022, entry version 122.
DE   RecName: Full=Glycerophosphodiester phosphodiesterase domain-containing protein 4;
DE            EC=3.1.-.-;
DE   AltName: Full=Glycerophosphodiester phosphodiesterase 6;
DE   AltName: Full=UgpQ;
GN   Name=GDPD4; Synonyms=GDE6, UGPQ;
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 [MRNA] (ISOFORMS 1 AND 2).
RA   Shan Y.X., Huang C.Q., Guo Z.K., Ye M.G., Yu L.;
RT   "Cloning and characterization of a novel GDPD gene.";
RL   Submitted (JUN-2003) to the EMBL/GenBank/DDBJ databases.
RN   [2]
RP   VARIANT LYS-396.
RX   PubMed=21248752; DOI=10.1038/nature09639;
RA   Varela I., Tarpey P., Raine K., Huang D., Ong C.K., Stephens P., Davies H.,
RA   Jones D., Lin M.L., Teague J., Bignell G., Butler A., Cho J.,
RA   Dalgliesh G.L., Galappaththige D., Greenman C., Hardy C., Jia M.,
RA   Latimer C., Lau K.W., Marshall J., McLaren S., Menzies A., Mudie L.,
RA   Stebbings L., Largaespada D.A., Wessels L.F.A., Richard S., Kahnoski R.J.,
RA   Anema J., Tuveson D.A., Perez-Mancera P.A., Mustonen V., Fischer A.,
RA   Adams D.J., Rust A., Chan-On W., Subimerb C., Dykema K., Furge K.,
RA   Campbell P.J., Teh B.T., Stratton M.R., Futreal P.A.;
RT   "Exome sequencing identifies frequent mutation of the SWI/SNF complex gene
RT   PBRM1 in renal carcinoma.";
RL   Nature 469:539-542(2011).
CC   -!- SUBCELLULAR LOCATION: Membrane {ECO:0000305}; Multi-pass membrane
CC       protein {ECO:0000305}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=2;
CC       Name=1;
CC         IsoId=Q6W3E5-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=Q6W3E5-2; Sequence=VSP_020811, VSP_020812;
CC   -!- SIMILARITY: Belongs to the glycerophosphoryl diester phosphodiesterase
CC       family. {ECO:0000305}.
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DR   EMBL; AY313782; AAQ72549.1; -; mRNA.
DR   EMBL; AY326450; AAP92403.1; -; mRNA.
DR   CCDS; CCDS8249.1; -. [Q6W3E5-2]
DR   RefSeq; NP_878253.1; NM_182833.1. [Q6W3E5-2]
DR   AlphaFoldDB; Q6W3E5; -.
DR   SMR; Q6W3E5; -.
DR   BioGRID; 128619; 2.
DR   IntAct; Q6W3E5; 2.
DR   STRING; 9606.ENSP00000320815; -.
DR   GlyGen; Q6W3E5; 2 sites.
DR   iPTMnet; Q6W3E5; -.
DR   PhosphoSitePlus; Q6W3E5; -.
DR   BioMuta; GDPD4; -.
DR   DMDM; 74710342; -.
DR   PaxDb; Q6W3E5; -.
DR   PeptideAtlas; Q6W3E5; -.
DR   PRIDE; Q6W3E5; -.
DR   DNASU; 220032; -.
DR   Ensembl; ENST00000315938.5; ENSP00000320815.4; ENSG00000178795.10. [Q6W3E5-2]
DR   Ensembl; ENST00000376217.6; ENSP00000365390.2; ENSG00000178795.10. [Q6W3E5-1]
DR   GeneID; 220032; -.
DR   KEGG; hsa:220032; -.
DR   MANE-Select; ENST00000315938.5; ENSP00000320815.4; NM_182833.3; NP_878253.1. [Q6W3E5-2]
DR   UCSC; uc001oyf.3; human. [Q6W3E5-1]
DR   CTD; 220032; -.
DR   GeneCards; GDPD4; -.
DR   HGNC; HGNC:24849; GDPD4.
DR   HPA; ENSG00000178795; Tissue enhanced (retina, testis).
DR   neXtProt; NX_Q6W3E5; -.
DR   OpenTargets; ENSG00000178795; -.
DR   PharmGKB; PA142671742; -.
DR   VEuPathDB; HostDB:ENSG00000178795; -.
DR   eggNOG; KOG2258; Eukaryota.
DR   GeneTree; ENSGT00940000156251; -.
DR   HOGENOM; CLU_024259_2_0_1; -.
DR   InParanoid; Q6W3E5; -.
DR   OMA; GFWFLWS; -.
DR   OrthoDB; 404866at2759; -.
DR   PhylomeDB; Q6W3E5; -.
DR   TreeFam; TF313692; -.
DR   PathwayCommons; Q6W3E5; -.
DR   SignaLink; Q6W3E5; -.
DR   BioGRID-ORCS; 220032; 3 hits in 1067 CRISPR screens.
DR   GenomeRNAi; 220032; -.
DR   Pharos; Q6W3E5; Tdark.
DR   PRO; PR:Q6W3E5; -.
DR   Proteomes; UP000005640; Chromosome 11.
DR   RNAct; Q6W3E5; protein.
DR   Bgee; ENSG00000178795; Expressed in right testis and 82 other tissues.
DR   GO; GO:0016021; C:integral component of membrane; IEA:UniProtKB-KW.
DR   GO; GO:0016020; C:membrane; IBA:GO_Central.
DR   GO; GO:0008889; F:glycerophosphodiester phosphodiesterase activity; IBA:GO_Central.
DR   GO; GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
DR   GO; GO:0006629; P:lipid metabolic process; IEA:InterPro.
DR   Gene3D; 3.20.20.190; -; 1.
DR   InterPro; IPR030395; GP_PDE_dom.
DR   InterPro; IPR017946; PLC-like_Pdiesterase_TIM-brl.
DR   Pfam; PF03009; GDPD; 1.
DR   SUPFAM; SSF51695; SSF51695; 1.
DR   PROSITE; PS51704; GP_PDE; 1.
PE   2: Evidence at transcript level;
KW   Alternative splicing; Glycoprotein; Hydrolase; Membrane; Metal-binding;
KW   Reference proteome; Transmembrane; Transmembrane helix.
FT   CHAIN           1..623
FT                   /note="Glycerophosphodiester phosphodiesterase domain-
FT                   containing protein 4"
FT                   /id="PRO_0000251938"
FT   TOPO_DOM        1..17
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        18..38
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        39
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        40..60
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        61..69
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        70..90
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        91..109
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        110..130
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        131..162
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        163..183
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        184..468
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        469..489
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        490..623
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   DOMAIN          198..457
FT                   /note="GP-PDE"
FT   BINDING         230
FT                   /ligand="a divalent metal cation"
FT                   /ligand_id="ChEBI:CHEBI:60240"
FT                   /evidence="ECO:0000255"
FT   BINDING         232
FT                   /ligand="a divalent metal cation"
FT                   /ligand_id="ChEBI:CHEBI:60240"
FT                   /evidence="ECO:0000255"
FT   BINDING         245
FT                   /ligand="a divalent metal cation"
FT                   /ligand_id="ChEBI:CHEBI:60240"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        308
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        397
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   VAR_SEQ         514..520
FT                   /note="NLHIAMK -> SKNEEDR (in isoform 2)"
FT                   /evidence="ECO:0000303|Ref.1"
FT                   /id="VSP_020811"
FT   VAR_SEQ         521..623
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|Ref.1"
FT                   /id="VSP_020812"
FT   VARIANT         220
FT                   /note="K -> R (in dbSNP:rs2729772)"
FT                   /id="VAR_055872"
FT   VARIANT         383
FT                   /note="H -> Y (in dbSNP:rs11237146)"
FT                   /id="VAR_055873"
FT   VARIANT         390
FT                   /note="I -> V (in dbSNP:rs11237145)"
FT                   /id="VAR_055874"
FT   VARIANT         396
FT                   /note="N -> K"
FT                   /evidence="ECO:0000269|PubMed:21248752"
FT                   /id="VAR_064764"
SQ   SEQUENCE   623 AA;  71996 MW;  5C8C81D1B735A365 CRC64;
     MLLFLWIETS SEYFNFDWVT FLGTGYWFFW SIFILSLARI LTAYSSLLLL LGFLLLWERI
     ELYLHLCHKI LILLVILLCV ILMFIICKFW KERWLVAGLS MQIFAPYVHL VSITVMVILF
     WPVAFYVACL EREVRMRRYR MTHSEKKRLK QCNVITRLRG LQVPVGLPFL LILLGLYLMP
     LGIYSPCIQE KENLGPKPTI FGHRGAPMLG PENTMMSFEK AVEHGAHGLE TDIHLSYDHV
     PFLMHDFDLK RTTNIGEVQP ESACENPAFF NWDFLSTLNA GKWFVKPELR PFYNMKPLSE
     ADKERARNQS IPTLADLLTL AEKERKFVIF DLHRPPPKHP LRHTFVRQVV SVILASKIEQ
     HLIFWLPAHD RQYVRSVAPG FQHVGRLVSI ETLAKNNISI INVDYKKLFP NGLRDYKAAN
     IHINVYTVNE PWLFSLAWCS RINSVTTDNI GLLSQLDHPH FFMTPKFYVF MWLLADIISV
     LFIVAIFCFH WRRETEKEKL FETSSTRTDT QSGNLHIAMK PPVRVVEGPW TLAALYPALP
     KSGKEHQGHF NFAAPSKKLL PIKNAVTPLK PGKHEIQPPM PTVVFELTQA PTRQATSEAT
     FQTTLPTLKV DKPTMPSIEV PYP
 
 
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