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GHDC_HUMAN
ID   GHDC_HUMAN              Reviewed;         530 AA.
AC   Q8N2G8; B4DQS4; E9PDB5; Q9BXM6;
DT   19-JUL-2004, integrated into UniProtKB/Swiss-Prot.
DT   19-JUL-2004, sequence version 2.
DT   03-AUG-2022, entry version 137.
DE   RecName: Full=GH3 domain-containing protein;
DE   Flags: Precursor;
GN   Name=GHDC; Synonyms=D11LGP1E, LGP1;
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] (ISOFORM 1).
RX   PubMed=11161808; DOI=10.1006/geno.2000.6433;
RA   Miyoshi K., Cui Y., Riedlinger G., Robinson P., Lehoczky J., Zon L.,
RA   Oka T., Dewar K., Hennighausen L.;
RT   "Structure of the mouse Stat 3/5 locus: evolution from Drosophila to
RT   zebrafish to mouse.";
RL   Genomics 71:150-155(2001).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1; 2 AND 3).
RC   TISSUE=Mammary gland, and Thyroid;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=16625196; DOI=10.1038/nature04689;
RA   Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R.,
RA   Nicholson C., Searle S.M., Wilming L., Young S.K., Abouelleil A.,
RA   Allen N.R., Bi W., Bloom T., Borowsky M.L., Bugalter B.E., Butler J.,
RA   Chang J.L., Chen C.-K., Cook A., Corum B., Cuomo C.A., de Jong P.J.,
RA   DeCaprio D., Dewar K., FitzGerald M., Gilbert J., Gibson R., Gnerre S.,
RA   Goldstein S., Grafham D.V., Grocock R., Hafez N., Hagopian D.S., Hart E.,
RA   Norman C.H., Humphray S., Jaffe D.B., Jones M., Kamal M., Khodiyar V.K.,
RA   LaButti K., Laird G., Lehoczky J., Liu X., Lokyitsang T., Loveland J.,
RA   Lui A., Macdonald P., Major J.E., Matthews L., Mauceli E., McCarroll S.A.,
RA   Mihalev A.H., Mudge J., Nguyen C., Nicol R., O'Leary S.B., Osoegawa K.,
RA   Schwartz D.C., Shaw-Smith C., Stankiewicz P., Steward C., Swarbreck D.,
RA   Venkataraman V., Whittaker C.A., Yang X., Zimmer A.R., Bradley A.,
RA   Hubbard T., Birren B.W., Rogers J., Lander E.S., Nusbaum C.;
RT   "DNA sequence of human chromosome 17 and analysis of rearrangement in the
RT   human lineage.";
RL   Nature 440:1045-1049(2006).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
RC   TISSUE=Colon;
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).
RN   [5]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RX   PubMed=21269460; DOI=10.1186/1752-0509-5-17;
RA   Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T.,
RA   Bennett K.L., Superti-Furga G., Colinge J.;
RT   "Initial characterization of the human central proteome.";
RL   BMC Syst. Biol. 5:17-17(2011).
RN   [6]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   TISSUE=Liver;
RX   PubMed=24275569; DOI=10.1016/j.jprot.2013.11.014;
RA   Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D., Wang L.,
RA   Ye M., Zou H.;
RT   "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver
RT   phosphoproteome.";
RL   J. Proteomics 96:253-262(2014).
RN   [7]
RP   METHYLATION AT GLN-489, AND MUTAGENESIS OF GLN-489.
RX   PubMed=26797129; DOI=10.1074/jbc.m115.711952;
RA   Kusevic D., Kudithipudi S., Jeltsch A.;
RT   "Substrate specificity of the HEMK2 protein glutamine methyltransferase and
RT   identification of novel substrates.";
RL   J. Biol. Chem. 291:6124-6133(2016).
CC   -!- SUBCELLULAR LOCATION: Endoplasmic reticulum
CC       {ECO:0000250|UniProtKB:Q99J23}. Nucleus envelope
CC       {ECO:0000250|UniProtKB:Q99J23}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=3;
CC       Name=1;
CC         IsoId=Q8N2G8-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=Q8N2G8-2; Sequence=VSP_010835, VSP_010836;
CC       Name=3;
CC         IsoId=Q8N2G8-3; Sequence=VSP_044831;
CC   -!- PTM: Methylated at Gln-489 by N6AMT1. {ECO:0000269|PubMed:26797129}.
CC   -!- SIMILARITY: Belongs to the GH3 family. {ECO:0000305}.
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DR   EMBL; AF316997; AAK15472.1; -; mRNA.
DR   EMBL; AK074700; BAC11146.1; -; mRNA.
DR   EMBL; AK075277; BAC11514.1; -; mRNA.
DR   EMBL; AK298933; BAG61036.1; -; mRNA.
DR   EMBL; AC099811; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; BC022784; AAH22784.1; -; mRNA.
DR   CCDS; CCDS11422.1; -. [Q8N2G8-1]
DR   CCDS; CCDS45682.1; -. [Q8N2G8-2]
DR   RefSeq; NP_001136095.1; NM_001142623.1. [Q8N2G8-2]
DR   RefSeq; NP_115873.1; NM_032484.4. [Q8N2G8-1]
DR   AlphaFoldDB; Q8N2G8; -.
DR   SMR; Q8N2G8; -.
DR   BioGRID; 124108; 67.
DR   IntAct; Q8N2G8; 26.
DR   STRING; 9606.ENSP00000301671; -.
DR   GlyGen; Q8N2G8; 2 sites, 1 O-linked glycan (1 site).
DR   iPTMnet; Q8N2G8; -.
DR   PhosphoSitePlus; Q8N2G8; -.
DR   BioMuta; GHDC; -.
DR   DMDM; 50401069; -.
DR   EPD; Q8N2G8; -.
DR   jPOST; Q8N2G8; -.
DR   MassIVE; Q8N2G8; -.
DR   MaxQB; Q8N2G8; -.
DR   PaxDb; Q8N2G8; -.
DR   PeptideAtlas; Q8N2G8; -.
DR   PRIDE; Q8N2G8; -.
DR   ProteomicsDB; 19626; -.
DR   ProteomicsDB; 71697; -. [Q8N2G8-1]
DR   ProteomicsDB; 71698; -. [Q8N2G8-2]
DR   Antibodypedia; 29163; 92 antibodies from 24 providers.
DR   DNASU; 84514; -.
DR   Ensembl; ENST00000301671.12; ENSP00000301671.7; ENSG00000167925.16. [Q8N2G8-1]
DR   Ensembl; ENST00000414034.7; ENSP00000399952.2; ENSG00000167925.16. [Q8N2G8-2]
DR   Ensembl; ENST00000428494.6; ENSP00000410945.3; ENSG00000167925.16. [Q8N2G8-2]
DR   Ensembl; ENST00000587427.6; ENSP00000467585.1; ENSG00000167925.16. [Q8N2G8-1]
DR   GeneID; 84514; -.
DR   KEGG; hsa:84514; -.
DR   MANE-Select; ENST00000587427.6; ENSP00000467585.1; NM_032484.5; NP_115873.1.
DR   UCSC; uc002hzd.4; human. [Q8N2G8-1]
DR   CTD; 84514; -.
DR   GeneCards; GHDC; -.
DR   HGNC; HGNC:24438; GHDC.
DR   HPA; ENSG00000167925; Low tissue specificity.
DR   MIM; 608587; gene.
DR   neXtProt; NX_Q8N2G8; -.
DR   OpenTargets; ENSG00000167925; -.
DR   PharmGKB; PA147358034; -.
DR   VEuPathDB; HostDB:ENSG00000167925; -.
DR   eggNOG; ENOG502QPMW; Eukaryota.
DR   GeneTree; ENSGT00390000016401; -.
DR   HOGENOM; CLU_038581_1_0_1; -.
DR   InParanoid; Q8N2G8; -.
DR   OMA; TSPWPHP; -.
DR   PhylomeDB; Q8N2G8; -.
DR   TreeFam; TF333007; -.
DR   PathwayCommons; Q8N2G8; -.
DR   Reactome; R-HSA-6798695; Neutrophil degranulation.
DR   SignaLink; Q8N2G8; -.
DR   BioGRID-ORCS; 84514; 14 hits in 1082 CRISPR screens.
DR   GenomeRNAi; 84514; -.
DR   Pharos; Q8N2G8; Tbio.
DR   PRO; PR:Q8N2G8; -.
DR   Proteomes; UP000005640; Chromosome 17.
DR   RNAct; Q8N2G8; protein.
DR   Bgee; ENSG00000167925; Expressed in right adrenal gland cortex and 139 other tissues.
DR   ExpressionAtlas; Q8N2G8; baseline and differential.
DR   Genevisible; Q8N2G8; HS.
DR   GO; GO:0005737; C:cytoplasm; IBA:GO_Central.
DR   GO; GO:0005783; C:endoplasmic reticulum; IEA:UniProtKB-SubCell.
DR   GO; GO:0005576; C:extracellular region; TAS:Reactome.
DR   GO; GO:0016020; C:membrane; HDA:UniProtKB.
DR   GO; GO:0005635; C:nuclear envelope; IEA:UniProtKB-SubCell.
DR   GO; GO:0034774; C:secretory granule lumen; TAS:Reactome.
DR   GO; GO:0035580; C:specific granule lumen; TAS:Reactome.
DR   GO; GO:0016881; F:acid-amino acid ligase activity; IBA:GO_Central.
DR   InterPro; IPR004993; GH3.
DR   PANTHER; PTHR31901; PTHR31901; 1.
DR   Pfam; PF03321; GH3; 1.
PE   1: Evidence at protein level;
KW   Alternative splicing; Endoplasmic reticulum; Glycoprotein; Methylation;
KW   Nucleus; Reference proteome; Signal.
FT   SIGNAL          1..17
FT                   /evidence="ECO:0000255"
FT   CHAIN           18..530
FT                   /note="GH3 domain-containing protein"
FT                   /id="PRO_0000021593"
FT   REGION          99..122
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   MOD_RES         489
FT                   /note="N5-methylglutamine"
FT                   /evidence="ECO:0000269|PubMed:26797129"
FT   CARBOHYD        450
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   VAR_SEQ         101..139
FT                   /note="Missing (in isoform 3)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_044831"
FT   VAR_SEQ         430..474
FT                   /note="DSSAGSAPHYEVFVALRGLRNLSEENRDKLDHCLQEASPRYKSLR -> EWG
FT                   RTDRAEDTRLGSCPFTGSMCAHGVYSQIPLRALLPTTRCLWR (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_010835"
FT   VAR_SEQ         475..530
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:14702039"
FT                   /id="VSP_010836"
FT   MUTAGEN         489
FT                   /note="Q->R: Abolishes methylation by N6AMT1."
FT                   /evidence="ECO:0000269|PubMed:26797129"
FT   CONFLICT        420
FT                   /note="D -> G (in Ref. 2; BAC11514)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   530 AA;  57523 MW;  BC0D92AC78889C16 CRC64;
     MLLWPLLLLL LLLPTLALLR QQRSQDARLS WLAGLQHRVA WGALVWAATW QRRRLEQSTL
     HVHQSQQQAL RWCLQGAQRP HCSLRRSTDI STFRNHLPLT KASQTQQEDS GEQPLPPTSN
     QDLGEASLQA TLLGLAALNK AYPEVLAQGR TARVTLTSPW PRPLPWPGNT LGQVGTPGTK
     DPRALLLDAL RSPGLRALEA GTAVELLDVF LGLETDGEEL AGAIAAGNPG APLRERAAEL
     REALEQGPRG LALRLWPKLQ VVVTLDAGGQ AEAVAALGAL WCQGLAFFSP AYAASGGVLG
     LNLQPEQPHG LYLLPPGAPF IELLPVKEGT QEEAASTLLL AEAQQGKEYE LVLTDRASLT
     RCRLGDVVRV VGAYNQCPVV RFICRLDQTL SVRGEDIGED LFSEALGRAV GQWAGAKLLD
     HGCVESSILD SSAGSAPHYE VFVALRGLRN LSEENRDKLD HCLQEASPRY KSLRFWGSVG
     PARVHLVGQG AFRALRAALA ACPSSPFPPA MPRVLRHRHL AQCLQERVVS
 
 
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