ID SRGEF_HUMAN Reviewed; 458 AA. AC Q9UGK8; Q9UGK9; DT 31-OCT-2003, integrated into UniProtKB/Swiss-Prot. DT 31-OCT-2003, sequence version 2. DT 03-AUG-2022, entry version 164. DE RecName: Full=Secretion-regulating guanine nucleotide exchange factor; DE AltName: Full=Deafness locus-associated putative guanine nucleotide exchange factor; DE Short=DelGEF; DE AltName: Full=Guanine nucleotide exchange factor-related protein; GN Name=SERGEF; Synonyms=DELGEF, GNEFR; 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), AND SUBCELLULAR LOCATION. RC TISSUE=Fetal brain; RX PubMed=10571079; DOI=10.1016/s0014-5793(99)01333-2; RA Uhlmann J., Wiemann S., Ponstingl H.; RT "DelGEF, an RCC1-related protein encoded by a gene on chromosome 11p14 RT critical for two forms of hereditary deafness."; RL FEBS Lett. 460:153-160(1999). RN [2] RP NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1). RC TISSUE=Ovary; 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 [3] RP INTERACTION WITH SEC5. RX PubMed=12459492; DOI=10.1016/s0014-5793(02)03677-3; RA Sjoelinder M., Uhlmann J., Ponstingl H.; RT "DelGEF, a homologue of the Ran guanine nucleotide exchange factor RanGEF, RT binds to the exocyst component Sec5 and modulates secretion."; RL FEBS Lett. 532:211-215(2002). RN [4] RP IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]. RC TISSUE=Embryonic kidney; RX PubMed=17525332; DOI=10.1126/science.1140321; RA Matsuoka S., Ballif B.A., Smogorzewska A., McDonald E.R. III, Hurov K.E., RA Luo J., Bakalarski C.E., Zhao Z., Solimini N., Lerenthal Y., Shiloh Y., RA Gygi S.P., Elledge S.J.; RT "ATM and ATR substrate analysis reveals extensive protein networks RT responsive to DNA damage."; RL Science 316:1160-1166(2007). RN [5] RP PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-427, AND IDENTIFICATION BY RP MASS SPECTROMETRY [LARGE SCALE ANALYSIS]. RC TISSUE=Erythroleukemia; RX PubMed=23186163; DOI=10.1021/pr300630k; RA Zhou H., Di Palma S., Preisinger C., Peng M., Polat A.N., Heck A.J., RA Mohammed S.; RT "Toward a comprehensive characterization of a human cancer cell RT phosphoproteome."; RL J. Proteome Res. 12:260-271(2013). CC -!- FUNCTION: Probable guanine nucleotide exchange factor (GEF), which may CC be involved in the secretion process. CC -!- SUBUNIT: Interacts with SEC5. The interaction occurs only in the CC presence of magnesium or manganese and is stimulated by dCTP or GTP. CC {ECO:0000269|PubMed:12459492}. CC -!- INTERACTION: CC Q9UGK8; Q96FX2: DPH3; NbExp=7; IntAct=EBI-465368, EBI-465363; CC Q9UGK8; O75593: FOXH1; NbExp=3; IntAct=EBI-465368, EBI-1759806; CC Q9UGK8; O14964: HGS; NbExp=3; IntAct=EBI-465368, EBI-740220; CC Q9UGK8; O60341: KDM1A; NbExp=2; IntAct=EBI-465368, EBI-710124; CC Q9UGK8; P78337: PITX1; NbExp=3; IntAct=EBI-465368, EBI-748265; CC Q9UGK8; Q96LA8: PRMT6; NbExp=2; IntAct=EBI-465368, EBI-912440; CC Q9UGK8; Q99932-2: SPAG8; NbExp=3; IntAct=EBI-465368, EBI-11959123; CC -!- SUBCELLULAR LOCATION: Cytoplasm {ECO:0000269|PubMed:10571079}. Nucleus CC {ECO:0000269|PubMed:10571079}. CC -!- ALTERNATIVE PRODUCTS: CC Event=Alternative splicing; Named isoforms=2; CC Name=1; Synonyms=DelGEF1; CC IsoId=Q9UGK8-1; Sequence=Displayed; CC Name=2; Synonyms=DelGEF2; CC IsoId=Q9UGK8-2; Sequence=VSP_050614, VSP_050615; CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; AJ243950; CAB60832.1; -; mRNA. DR EMBL; AJ243951; CAB60833.1; -; mRNA. DR EMBL; BC065375; AAH65375.1; -; mRNA. DR CCDS; CCDS7828.1; -. [Q9UGK8-1] DR RefSeq; NP_036271.1; NM_012139.3. [Q9UGK8-1] DR AlphaFoldDB; Q9UGK8; -. DR SMR; Q9UGK8; -. DR BioGRID; 117674; 12. DR IntAct; Q9UGK8; 9. DR MINT; Q9UGK8; -. DR STRING; 9606.ENSP00000265965; -. DR GlyGen; Q9UGK8; 1 site, 1 O-linked glycan (1 site). DR iPTMnet; Q9UGK8; -. DR PhosphoSitePlus; Q9UGK8; -. DR BioMuta; SERGEF; -. DR DMDM; 38257790; -. DR EPD; Q9UGK8; -. DR jPOST; Q9UGK8; -. DR MassIVE; Q9UGK8; -. DR MaxQB; Q9UGK8; -. DR PaxDb; Q9UGK8; -. DR PeptideAtlas; Q9UGK8; -. DR PRIDE; Q9UGK8; -. DR ProteomicsDB; 84229; -. [Q9UGK8-1] DR ProteomicsDB; 84230; -. [Q9UGK8-2] DR Antibodypedia; 12179; 102 antibodies from 22 providers. DR DNASU; 26297; -. DR Ensembl; ENST00000265965.10; ENSP00000265965.5; ENSG00000129158.11. [Q9UGK8-1] DR Ensembl; ENST00000528200.5; ENSP00000434188.1; ENSG00000129158.11. [Q9UGK8-2] DR GeneID; 26297; -. DR KEGG; hsa:26297; -. DR MANE-Select; ENST00000265965.10; ENSP00000265965.5; NM_012139.4; NP_036271.1. DR UCSC; uc001mnm.5; human. [Q9UGK8-1] DR CTD; 26297; -. DR DisGeNET; 26297; -. DR GeneCards; SERGEF; -. DR HGNC; HGNC:17499; SERGEF. DR HPA; ENSG00000129158; Low tissue specificity. DR MIM; 606051; gene. DR neXtProt; NX_Q9UGK8; -. DR OpenTargets; ENSG00000129158; -. DR PharmGKB; PA143485610; -. DR VEuPathDB; HostDB:ENSG00000129158; -. DR eggNOG; KOG1426; Eukaryota. DR GeneTree; ENSGT00940000160684; -. DR HOGENOM; CLU_005210_0_3_1; -. DR InParanoid; Q9UGK8; -. DR OMA; GYESELC; -. DR PhylomeDB; Q9UGK8; -. DR TreeFam; TF330842; -. DR PathwayCommons; Q9UGK8; -. DR SignaLink; Q9UGK8; -. DR BioGRID-ORCS; 26297; 16 hits in 1090 CRISPR screens. DR ChiTaRS; SERGEF; human. DR GenomeRNAi; 26297; -. DR Pharos; Q9UGK8; Tdark. DR PRO; PR:Q9UGK8; -. DR Proteomes; UP000005640; Chromosome 11. DR RNAct; Q9UGK8; protein. DR Bgee; ENSG00000129158; Expressed in right frontal lobe and 166 other tissues. DR ExpressionAtlas; Q9UGK8; baseline and differential. DR Genevisible; Q9UGK8; HS. DR GO; GO:0005737; C:cytoplasm; IDA:UniProtKB. DR GO; GO:0005829; C:cytosol; IDA:HPA. DR GO; GO:0005654; C:nucleoplasm; IDA:HPA. DR GO; GO:0005634; C:nucleus; IDA:UniProtKB. DR GO; GO:0005085; F:guanyl-nucleotide exchange factor activity; TAS:UniProtKB. DR GO; GO:0061630; F:ubiquitin protein ligase activity; IBA:GO_Central. DR GO; GO:0050709; P:negative regulation of protein secretion; IDA:HGNC-UCL. DR GO; GO:0016567; P:protein ubiquitination; IBA:GO_Central. DR GO; GO:0007165; P:signal transduction; TAS:UniProtKB. DR GO; GO:0006511; P:ubiquitin-dependent protein catabolic process; IBA:GO_Central. DR Gene3D; 2.130.10.30; -; 2. DR InterPro; IPR009091; RCC1/BLIP-II. DR InterPro; IPR000408; Reg_chr_condens. DR Pfam; PF00415; RCC1; 5. DR PRINTS; PR00633; RCCNDNSATION. DR SUPFAM; SSF50985; SSF50985; 1. DR PROSITE; PS00626; RCC1_2; 2. DR PROSITE; PS50012; RCC1_3; 7. PE 1: Evidence at protein level; KW Alternative splicing; Cytoplasm; Guanine-nucleotide releasing factor; KW Nucleus; Phosphoprotein; Reference proteome; Repeat. FT CHAIN 1..458 FT /note="Secretion-regulating guanine nucleotide exchange FT factor" FT /id="PRO_0000206649" FT REPEAT 15..67 FT /note="RCC1 1" FT REPEAT 68..119 FT /note="RCC1 2" FT REPEAT 120..171 FT /note="RCC1 3" FT REPEAT 172..230 FT /note="RCC1 4" FT REPEAT 231..283 FT /note="RCC1 5" FT REPEAT 284..351 FT /note="RCC1 6" FT REPEAT 352..402 FT /note="RCC1 7" FT REGION 420..458 FT /note="Disordered" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT COMPBIAS 425..441 FT /note="Basic and acidic residues" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT COMPBIAS 442..458 FT /note="Polar residues" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT MOD_RES 427 FT /note="Phosphoserine" FT /evidence="ECO:0007744|PubMed:23186163" FT VAR_SEQ 282..288 FT /note="ETGKMFT -> GLLWLRA (in isoform 2)" FT /evidence="ECO:0000303|PubMed:10571079" FT /id="VSP_050614" FT VAR_SEQ 289..458 FT /note="Missing (in isoform 2)" FT /evidence="ECO:0000303|PubMed:10571079" FT /id="VSP_050615" FT VARIANT 429 FT /note="K -> E (in dbSNP:rs1528)" FT /id="VAR_017156" FT VARIANT 457 FT /note="G -> E (in dbSNP:rs10788)" FT /id="VAR_017157" SQ SEQUENCE 458 AA; 48981 MW; 0284B7E4A88F2A7C CRC64; MEREPSASEA APAAAALFAW GANSYGQLGL GHKEDVLLPQ QLNDFCKPRS VRRITGGGGH SAVVTDGGDL FVCGLNKDGQ LGLGHTEDIP YFTPCKSLFG CPIQQVACGW DFTIMLTENG QVLSCGSNSF GQLGVPHGPR RCVVPQAIEL HKEKVVCIAA GLRHAVAATA SGIVFQWGTG LASCGRRLCP GQTLPLFFTA KEPSRVTGLE NSKAMCVLAG SDHSASLTDA GEVYVWGSNK HGQLANEAAF LPVPQKIEAH CFQNEKVTAI WSGWTHLVAQ TETGKMFTWG RADYGQLGRK LETYEGWKLE KQDSFLPCSR PPNSMPSSPH CLTGATEVSC GSEHNLAIIG GVCYSWGWNE HGMCGDGTEA NVWAPKPVQA LLSSSGLLVG CGAGHSLALC QLPAHPALVQ DPKVTYLSPD AIEDTESQKA MDKERNWKER QSETSTQSQS DWSRNGGL //