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BORG2_HUMAN
ID   BORG2_HUMAN             Reviewed;         254 AA.
AC   Q9UKI2; B2R8S0; O95353; Q9UQJ0;
DT   19-JUL-2005, integrated into UniProtKB/Swiss-Prot.
DT   01-MAY-2000, sequence version 1.
DT   03-AUG-2022, entry version 156.
DE   RecName: Full=Cdc42 effector protein 3;
DE   AltName: Full=Binder of Rho GTPases 2;
DE   AltName: Full=MSE55-related Cdc42-binding protein;
GN   Name=CDC42EP3; Synonyms=BORG2, CEP3;
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], FUNCTION, TISSUE SPECIFICITY, AND INTERACTION
RP   WITH RHOQ AND CDC42.
RC   TISSUE=Heart;
RX   PubMed=10490598; DOI=10.1128/mcb.19.10.6585;
RA   Joberty G., Perlungher R.R., Macara I.G.;
RT   "The Borgs, a new family of Cdc42 and TC10 GTPase-interacting proteins.";
RL   Mol. Cell. Biol. 19:6585-6597(1999).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, AND SUBCELLULAR LOCATION.
RC   TISSUE=Uterus;
RX   PubMed=11035016; DOI=10.1074/jbc.m007039200;
RA   Hirsch D.S., Pirone D.M., Burbelo P.D.;
RT   "A new family of Cdc42 effector proteins, CEPs, function in fibroblast and
RT   epithelial cell shape changes.";
RL   J. Biol. Chem. 276:875-883(2001).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [MRNA].
RC   TISSUE=Brain;
RA   Alberts A.S.;
RT   "MSE55-related Cdc42-binding protein.";
RL   Submitted (SEP-1998) to the EMBL/GenBank/DDBJ databases.
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Testis;
RX   PubMed=11230166; DOI=10.1101/gr.gr1547r;
RA   Wiemann S., Weil B., Wellenreuther R., Gassenhuber J., Glassl S.,
RA   Ansorge W., Boecher M., Bloecker H., Bauersachs S., Blum H., Lauber J.,
RA   Duesterhoeft A., Beyer A., Koehrer K., Strack N., Mewes H.-W.,
RA   Ottenwaelder B., Obermaier B., Tampe J., Heubner D., Wambutt R., Korn B.,
RA   Klein M., Poustka A.;
RT   "Towards a catalog of human genes and proteins: sequencing and analysis of
RT   500 novel complete protein coding human cDNAs.";
RL   Genome Res. 11:422-435(2001).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RA   Kalnine N., Chen X., Rolfs A., Halleck A., Hines L., Eisenstein S.,
RA   Koundinya M., Raphael J., Moreira D., Kelley T., LaBaer J., Lin Y.,
RA   Phelan M., Farmer A.;
RT   "Cloning of human full-length CDSs in BD Creator(TM) system donor vector.";
RL   Submitted (MAY-2003) to the EMBL/GenBank/DDBJ databases.
RN   [6]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Cervix;
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   [7]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=15815621; DOI=10.1038/nature03466;
RA   Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P.,
RA   Wagner-McPherson C., Layman D., Wylie K., Sekhon M., Becker M.C.,
RA   Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Kremitzki C., Oddy L.,
RA   Du H., Sun H., Bradshaw-Cordum H., Ali J., Carter J., Cordes M., Harris A.,
RA   Isak A., van Brunt A., Nguyen C., Du F., Courtney L., Kalicki J.,
RA   Ozersky P., Abbott S., Armstrong J., Belter E.A., Caruso L., Cedroni M.,
RA   Cotton M., Davidson T., Desai A., Elliott G., Erb T., Fronick C., Gaige T.,
RA   Haakenson W., Haglund K., Holmes A., Harkins R., Kim K., Kruchowski S.S.,
RA   Strong C.M., Grewal N., Goyea E., Hou S., Levy A., Martinka S., Mead K.,
RA   McLellan M.D., Meyer R., Randall-Maher J., Tomlinson C.,
RA   Dauphin-Kohlberg S., Kozlowicz-Reilly A., Shah N., Swearengen-Shahid S.,
RA   Snider J., Strong J.T., Thompson J., Yoakum M., Leonard S., Pearman C.,
RA   Trani L., Radionenko M., Waligorski J.E., Wang C., Rock S.M.,
RA   Tin-Wollam A.-M., Maupin R., Latreille P., Wendl M.C., Yang S.-P., Pohl C.,
RA   Wallis J.W., Spieth J., Bieri T.A., Berkowicz N., Nelson J.O., Osborne J.,
RA   Ding L., Meyer R., Sabo A., Shotland Y., Sinha P., Wohldmann P.E.,
RA   Cook L.L., Hickenbotham M.T., Eldred J., Williams D., Jones T.A., She X.,
RA   Ciccarelli F.D., Izaurralde E., Taylor J., Schmutz J., Myers R.M.,
RA   Cox D.R., Huang X., McPherson J.D., Mardis E.R., Clifton S.W., Warren W.C.,
RA   Chinwalla A.T., Eddy S.R., Marra M.A., Ovcharenko I., Furey T.S.,
RA   Miller W., Eichler E.E., Bork P., Suyama M., Torrents D., Waterston R.H.,
RA   Wilson R.K.;
RT   "Generation and annotation of the DNA sequences of human chromosomes 2 and
RT   4.";
RL   Nature 434:724-731(2005).
RN   [8]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases.
RN   [9]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Lung;
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   [10]
RP   INTERACTION WITH SEPT7.
RX   PubMed=11584266; DOI=10.1038/ncb1001-861;
RA   Joberty G., Perlungher R.R., Sheffield P.J., Kinoshita M., Noda M.,
RA   Haystead T., Macara I.G.;
RT   "Borg proteins control septin organization and are negatively regulated by
RT   Cdc42.";
RL   Nat. Cell Biol. 3:861-866(2001).
RN   [11]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RX   PubMed=22814378; DOI=10.1073/pnas.1210303109;
RA   Van Damme P., Lasa M., Polevoda B., Gazquez C., Elosegui-Artola A.,
RA   Kim D.S., De Juan-Pardo E., Demeyer K., Hole K., Larrea E., Timmerman E.,
RA   Prieto J., Arnesen T., Sherman F., Gevaert K., Aldabe R.;
RT   "N-terminal acetylome analyses and functional insights of the N-terminal
RT   acetyltransferase NatB.";
RL   Proc. Natl. Acad. Sci. U.S.A. 109:12449-12454(2012).
RN   [12]
RP   PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-89, 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).
RN   [13]
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).
CC   -!- FUNCTION: Probably involved in the organization of the actin
CC       cytoskeleton. May act downstream of CDC42 to induce actin filament
CC       assembly leading to cell shape changes. Induces pseudopodia formation
CC       in fibroblasts. {ECO:0000269|PubMed:10490598,
CC       ECO:0000269|PubMed:11035016}.
CC   -!- SUBUNIT: Interacts with RHOQ and CDC42, in a GTP-dependent manner, and
CC       with SEPT7. {ECO:0000269|PubMed:10490598, ECO:0000269|PubMed:11584266}.
CC   -!- INTERACTION:
CC       Q9UKI2; O14579: COPE; NbExp=3; IntAct=EBI-723480, EBI-711301;
CC       Q9UKI2; Q5S007: LRRK2; NbExp=2; IntAct=EBI-723480, EBI-5323863;
CC   -!- SUBCELLULAR LOCATION: Endomembrane system
CC       {ECO:0000269|PubMed:11035016}; Peripheral membrane protein
CC       {ECO:0000269|PubMed:11035016}. Cytoplasm, cytoskeleton
CC       {ECO:0000269|PubMed:11035016}.
CC   -!- TISSUE SPECIFICITY: Highly expressed in the heart and weakly in the
CC       brain. {ECO:0000269|PubMed:10490598}.
CC   -!- SIMILARITY: Belongs to the BORG/CEP family. {ECO:0000305}.
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DR   EMBL; AF164118; AAD48815.1; -; mRNA.
DR   EMBL; AF104857; AAD16888.1; -; mRNA.
DR   EMBL; AF094521; AAC71773.1; -; mRNA.
DR   EMBL; AL136842; CAB66776.1; -; mRNA.
DR   EMBL; BT007190; AAP35854.1; -; mRNA.
DR   EMBL; AK313483; BAG36267.1; -; mRNA.
DR   EMBL; AC006369; AAX93072.1; -; Genomic_DNA.
DR   EMBL; CH471053; EAX00390.1; -; Genomic_DNA.
DR   EMBL; BC019270; AAH19270.1; -; mRNA.
DR   CCDS; CCDS1791.1; -.
DR   PIR; T46465; T46465.
DR   RefSeq; NP_001257365.1; NM_001270436.1.
DR   RefSeq; NP_001257366.1; NM_001270437.1.
DR   RefSeq; NP_001257367.1; NM_001270438.1.
DR   RefSeq; NP_006440.2; NM_006449.4.
DR   RefSeq; XP_011530784.1; XM_011532482.2.
DR   AlphaFoldDB; Q9UKI2; -.
DR   BioGRID; 115849; 15.
DR   IntAct; Q9UKI2; 9.
DR   STRING; 9606.ENSP00000295324; -.
DR   GlyGen; Q9UKI2; 1 site, 1 O-linked glycan (1 site).
DR   iPTMnet; Q9UKI2; -.
DR   PhosphoSitePlus; Q9UKI2; -.
DR   BioMuta; CDC42EP3; -.
DR   DMDM; 71152340; -.
DR   CPTAC; CPTAC-961; -.
DR   EPD; Q9UKI2; -.
DR   jPOST; Q9UKI2; -.
DR   MassIVE; Q9UKI2; -.
DR   MaxQB; Q9UKI2; -.
DR   PaxDb; Q9UKI2; -.
DR   PeptideAtlas; Q9UKI2; -.
DR   PRIDE; Q9UKI2; -.
DR   ProteomicsDB; 84789; -.
DR   Antibodypedia; 29451; 213 antibodies from 27 providers.
DR   DNASU; 10602; -.
DR   Ensembl; ENST00000295324.4; ENSP00000295324.3; ENSG00000163171.8.
DR   Ensembl; ENST00000611976.1; ENSP00000480549.1; ENSG00000163171.8.
DR   GeneID; 10602; -.
DR   KEGG; hsa:10602; -.
DR   MANE-Select; ENST00000295324.4; ENSP00000295324.3; NM_006449.5; NP_006440.2.
DR   UCSC; uc002rqi.3; human.
DR   CTD; 10602; -.
DR   DisGeNET; 10602; -.
DR   GeneCards; CDC42EP3; -.
DR   HGNC; HGNC:16943; CDC42EP3.
DR   HPA; ENSG00000163171; Low tissue specificity.
DR   MIM; 606133; gene.
DR   neXtProt; NX_Q9UKI2; -.
DR   OpenTargets; ENSG00000163171; -.
DR   PharmGKB; PA38429; -.
DR   VEuPathDB; HostDB:ENSG00000163171; -.
DR   eggNOG; ENOG502RKYM; Eukaryota.
DR   GeneTree; ENSGT00940000157736; -.
DR   HOGENOM; CLU_073229_0_0_1; -.
DR   InParanoid; Q9UKI2; -.
DR   OMA; LPTIGGC; -.
DR   OrthoDB; 1244464at2759; -.
DR   PhylomeDB; Q9UKI2; -.
DR   TreeFam; TF331725; -.
DR   PathwayCommons; Q9UKI2; -.
DR   Reactome; R-HSA-5687128; MAPK6/MAPK4 signaling.
DR   Reactome; R-HSA-9013148; CDC42 GTPase cycle.
DR   Reactome; R-HSA-9013406; RHOQ GTPase cycle.
DR   SignaLink; Q9UKI2; -.
DR   BioGRID-ORCS; 10602; 10 hits in 1077 CRISPR screens.
DR   ChiTaRS; CDC42EP3; human.
DR   GeneWiki; CDC42EP3; -.
DR   GenomeRNAi; 10602; -.
DR   Pharos; Q9UKI2; Tbio.
DR   PRO; PR:Q9UKI2; -.
DR   Proteomes; UP000005640; Chromosome 2.
DR   RNAct; Q9UKI2; protein.
DR   Bgee; ENSG00000163171; Expressed in tibia and 197 other tissues.
DR   ExpressionAtlas; Q9UKI2; baseline and differential.
DR   Genevisible; Q9UKI2; HS.
DR   GO; GO:0015629; C:actin cytoskeleton; IDA:LIFEdb.
DR   GO; GO:0005737; C:cytoplasm; IBA:GO_Central.
DR   GO; GO:0005856; C:cytoskeleton; IBA:GO_Central.
DR   GO; GO:0005829; C:cytosol; TAS:Reactome.
DR   GO; GO:0012505; C:endomembrane system; IEA:UniProtKB-SubCell.
DR   GO; GO:0005886; C:plasma membrane; IDA:HPA.
DR   GO; GO:0005519; F:cytoskeletal regulatory protein binding; TAS:ProtInc.
DR   GO; GO:0030838; P:positive regulation of actin filament polymerization; IBA:GO_Central.
DR   GO; GO:0031274; P:positive regulation of pseudopodium assembly; IBA:GO_Central.
DR   GO; GO:0008360; P:regulation of cell shape; IBA:GO_Central.
DR   GO; GO:0007266; P:Rho protein signal transduction; IBA:GO_Central.
DR   GO; GO:0007165; P:signal transduction; TAS:ProtInc.
DR   InterPro; IPR029273; Cdc42_effect.
DR   InterPro; IPR000095; CRIB_dom.
DR   Pfam; PF14957; BORG_CEP; 1.
DR   Pfam; PF00786; PBD; 1.
DR   SMART; SM00285; PBD; 1.
DR   PROSITE; PS50108; CRIB; 1.
PE   1: Evidence at protein level;
KW   Cell shape; Cytoplasm; Cytoskeleton; Membrane; Phosphoprotein;
KW   Reference proteome.
FT   CHAIN           1..254
FT                   /note="Cdc42 effector protein 3"
FT                   /id="PRO_0000212651"
FT   DOMAIN          31..45
FT                   /note="CRIB"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00057"
FT   REGION          164..225
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        164..196
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        208..222
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   MOD_RES         63
FT                   /note="Phosphotyrosine"
FT                   /evidence="ECO:0000250|UniProtKB:Q9CQC5"
FT   MOD_RES         89
FT                   /note="Phosphoserine"
FT                   /evidence="ECO:0007744|PubMed:23186163"
FT   MOD_RES         108
FT                   /note="Phosphoserine"
FT                   /evidence="ECO:0000250|UniProtKB:Q9CQC5"
FT   MOD_RES         144
FT                   /note="Phosphoserine"
FT                   /evidence="ECO:0000250|UniProtKB:Q9CQC5"
FT   CONFLICT        56
FT                   /note="I -> N (in Ref. 2; AAD16888)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        233
FT                   /note="S -> F (in Ref. 3; AAC71773)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   254 AA;  27678 MW;  C31CDBE151C161ED CRC64;
     MPAKTPIYLK AANNKKGKKF KLRDILSPDM ISPPLGDFRH TIHIGKEGQH DVFGDISFLQ
     GNYELLPGNQ EKAHLGQFPG HNEFFRANST SDSVFTETPS PVLKNAISLP TIGGSQALML
     PLLSPVTFNS KQESFGPAKL PRLSCEPVME EKAQEKSSLL ENGTVHQGDT SWGSSGSASQ
     SSQGRDSHSS SLSEQYPDWP AEDMFDHPTP CELIKGKTKS EESLSDLTGS LLSLQLDLGP
     SLLDEVLNVM DKNK
 
 
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