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Database: UniProt
Entry: YJEN3_HUMAN
LinkDB: YJEN3_HUMAN
Original site: YJEN3_HUMAN 
ID   YJEN3_HUMAN             Reviewed;         299 AA.
AC   A6XGL0; A6XGK9; Q4G1C0;
DT   02-SEP-2008, integrated into UniProtKB/Swiss-Prot.
DT   21-AUG-2007, sequence version 1.
DT   24-JAN-2024, entry version 115.
DE   RecName: Full=YjeF N-terminal domain-containing protein 3 {ECO:0000305};
DE            Short=YjeF_N3;
DE            Short=hYjeF_N3;
DE   AltName: Full=ApoA-I-binding protein 2 {ECO:0000250|UniProtKB:Q1LVI2};
GN   Name=YJEFN3; Synonyms=AIBP2 {ECO:0000250|UniProtKB:Q1LVI2};
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   Yu Z., Zheng Z., Tang T., Fu Y.;
RT   "A computer system platform used to predict novel genes and some proteins
RT   similar to apolipoprotein a1 binding protein.";
RL   Submitted (JUN-2006) to the EMBL/GenBank/DDBJ databases.
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=15057824; DOI=10.1038/nature02399;
RA   Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E.,
RA   Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M., Aerts A.,
RA   Altherr M., Ashworth L., Bajorek E., Black S., Branscomb E., Caenepeel S.,
RA   Carrano A.V., Caoile C., Chan Y.M., Christensen M., Cleland C.A.,
RA   Copeland A., Dalin E., Dehal P., Denys M., Detter J.C., Escobar J.,
RA   Flowers D., Fotopulos D., Garcia C., Georgescu A.M., Glavina T., Gomez M.,
RA   Gonzales E., Groza M., Hammon N., Hawkins T., Haydu L., Ho I., Huang W.,
RA   Israni S., Jett J., Kadner K., Kimball H., Kobayashi A., Larionov V.,
RA   Leem S.-H., Lopez F., Lou Y., Lowry S., Malfatti S., Martinez D.,
RA   McCready P.M., Medina C., Morgan J., Nelson K., Nolan M., Ovcharenko I.,
RA   Pitluck S., Pollard M., Popkie A.P., Predki P., Quan G., Ramirez L.,
RA   Rash S., Retterer J., Rodriguez A., Rogers S., Salamov A., Salazar A.,
RA   She X., Smith D., Slezak T., Solovyev V., Thayer N., Tice H., Tsai M.,
RA   Ustaszewska A., Vo N., Wagner M., Wheeler J., Wu K., Xie G., Yang J.,
RA   Dubchak I., Furey T.S., DeJong P., Dickson M., Gordon D., Eichler E.E.,
RA   Pennacchio L.A., Richardson P., Stubbs L., Rokhsar D.S., Myers R.M.,
RA   Rubin E.M., Lucas S.M.;
RT   "The DNA sequence and biology of human chromosome 19.";
RL   Nature 428:529-535(2004).
RN   [3]
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 (JUL-2005) to the EMBL/GenBank/DDBJ databases.
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
RC   TISSUE=Brain;
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   FUNCTION, AND TISSUE SPECIFICITY.
RX   PubMed=17533573; DOI=10.1055/s-2007-977699;
RA   Rudolph C., Sigruener A., Hartmann A., Orso E., Bals-Pratsch M.,
RA   Gronwald W., Seifert B., Kalbitzer H.R., Verdorfer I., Luetjens C.M.,
RA   Ortmann O., Bornstein S.R., Schmitz G.;
RT   "ApoA-I-binding protein (AI-BP) and its homologues hYjeF_N2 and hYjeF_N3
RT   comprise the YjeF_N domain protein family in humans with a role in
RT   spermiogenesis and oogenesis.";
RL   Horm. Metab. Res. 39:322-335(2007).
RN   [6]
RP   INTERACTION WITH APOA1.
RX   PubMed=23719382; DOI=10.1038/nature12166;
RA   Fang L., Choi S.H., Baek J.S., Liu C., Almazan F., Ulrich F., Wiesner P.,
RA   Taleb A., Deer E., Pattison J., Torres-Vazquez J., Li A.C., Miller Y.I.;
RT   "Control of angiogenesis by AIBP-mediated cholesterol efflux.";
RL   Nature 498:118-122(2013).
CC   -!- FUNCTION: May accelerate cholesterol efflux from endothelial cells to
CC       high-density lipoprotein (HDL) and thereby regulates angiogenesis. May
CC       orchestrate hematopoietic stem and progenitor cell emergence from the
CC       hemogenic endothelium, a type of specialized endothelium manifesting
CC       hematopoietic potential. YJEFN3-mediated cholesterol efflux activates
CC       endothelial SREBF2, the master transcription factor for cholesterol
CC       biosynthesis, which in turn transactivates NOTCH and promotes
CC       hematopoietic stem and progenitor cell emergence (By similarity). May
CC       play a role in spermiogenesis and oogenesis (PubMed:17533573).
CC       {ECO:0000250|UniProtKB:Q1LVI2, ECO:0000269|PubMed:17533573}.
CC   -!- SUBUNIT: Interacts with APOA1 (PubMed:23719382). Binds to HDL
CC       (PubMed:17533573). {ECO:0000269|PubMed:17533573,
CC       ECO:0000269|PubMed:23719382}.
CC   -!- INTERACTION:
CC       A6XGL0; P28062-2: PSMB8; NbExp=3; IntAct=EBI-13070200, EBI-372312;
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=2;
CC       Name=1;
CC         IsoId=A6XGL0-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=A6XGL0-2; Sequence=VSP_035170;
CC   -!- TISSUE SPECIFICITY: Expressed in theca cells in ovary and in Leydig
CC       cells in testis (at protein level). Also expressed in brain and mammary
CC       gland. {ECO:0000269|PubMed:17533573}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=BC020948; Type=Frameshift; Evidence={ECO:0000305};
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DR   EMBL; DQ778080; ABI63344.1; -; mRNA.
DR   EMBL; DQ778079; ABI63349.1; -; mRNA.
DR   EMBL; AC011448; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH471106; EAW84827.1; -; Genomic_DNA.
DR   EMBL; BC020948; -; NOT_ANNOTATED_CDS; mRNA.
DR   CCDS; CCDS42530.1; -. [A6XGL0-1]
DR   CCDS; CCDS54236.1; -. [A6XGL0-2]
DR   RefSeq; NP_001177257.1; NM_001190328.1. [A6XGL0-2]
DR   RefSeq; NP_940939.2; NM_198537.3. [A6XGL0-1]
DR   AlphaFoldDB; A6XGL0; -.
DR   SMR; A6XGL0; -.
DR   BioGRID; 131931; 16.
DR   IntAct; A6XGL0; 1.
DR   STRING; 9606.ENSP00000426964; -.
DR   iPTMnet; A6XGL0; -.
DR   PhosphoSitePlus; A6XGL0; -.
DR   BioMuta; YJEFN3; -.
DR   MassIVE; A6XGL0; -.
DR   PaxDb; 9606-ENSP00000426964; -.
DR   PeptideAtlas; A6XGL0; -.
DR   ProteomicsDB; 1760; -. [A6XGL0-1]
DR   ProteomicsDB; 1761; -. [A6XGL0-2]
DR   Antibodypedia; 54853; 10 antibodies from 7 providers.
DR   DNASU; 374887; -.
DR   Ensembl; ENST00000436027.9; ENSP00000398520.2; ENSG00000250067.12. [A6XGL0-2]
DR   Ensembl; ENST00000514277.6; ENSP00000426964.1; ENSG00000250067.12. [A6XGL0-1]
DR   GeneID; 374887; -.
DR   KEGG; hsa:374887; -.
DR   MANE-Select; ENST00000514277.6; ENSP00000426964.1; NM_198537.4; NP_940939.2.
DR   UCSC; uc002nmt.3; human. [A6XGL0-1]
DR   AGR; HGNC:24785; -.
DR   CTD; 374887; -.
DR   DisGeNET; 374887; -.
DR   GeneCards; YJEFN3; -.
DR   HGNC; HGNC:24785; YJEFN3.
DR   HPA; ENSG00000250067; Tissue enriched (brain).
DR   MIM; 618607; gene.
DR   neXtProt; NX_A6XGL0; -.
DR   OpenTargets; ENSG00000250067; -.
DR   PharmGKB; PA164727608; -.
DR   VEuPathDB; HostDB:ENSG00000250067; -.
DR   eggNOG; KOG2585; Eukaryota.
DR   GeneTree; ENSGT00390000007227; -.
DR   HOGENOM; CLU_024853_3_0_1; -.
DR   InParanoid; A6XGL0; -.
DR   OMA; HSCAMAV; -.
DR   OrthoDB; 1493at2759; -.
DR   PhylomeDB; A6XGL0; -.
DR   TreeFam; TF300197; -.
DR   PathwayCommons; A6XGL0; -.
DR   SignaLink; A6XGL0; -.
DR   BioGRID-ORCS; 374887; 69 hits in 1154 CRISPR screens.
DR   ChiTaRS; YJEFN3; human.
DR   GenomeRNAi; 374887; -.
DR   Pharos; A6XGL0; Tdark.
DR   PRO; PR:A6XGL0; -.
DR   Proteomes; UP000005640; Chromosome 19.
DR   RNAct; A6XGL0; Protein.
DR   Bgee; ENSG00000250067; Expressed in putamen and 98 other cell types or tissues.
DR   ExpressionAtlas; A6XGL0; baseline and differential.
DR   Genevisible; A6XGL0; HS.
DR   GO; GO:0052856; F:NADHX epimerase activity; IBA:GO_Central.
DR   GO; GO:0071425; P:hematopoietic stem cell proliferation; ISS:UniProtKB.
DR   GO; GO:0006869; P:lipid transport; IEA:UniProtKB-KW.
DR   GO; GO:0031580; P:membrane raft distribution; ISS:UniProtKB.
DR   GO; GO:0016525; P:negative regulation of angiogenesis; ISS:UniProtKB.
DR   GO; GO:0010874; P:regulation of cholesterol efflux; ISS:UniProtKB.
DR   GO; GO:0008593; P:regulation of Notch signaling pathway; ISS:UniProtKB.
DR   GO; GO:0002040; P:sprouting angiogenesis; ISS:UniProtKB.
DR   Gene3D; 3.40.50.10260; YjeF N-terminal domain; 1.
DR   InterPro; IPR004443; YjeF_N_dom.
DR   InterPro; IPR036652; YjeF_N_dom_sf.
DR   InterPro; IPR032976; YJEFN_prot_NAXE-like.
DR   NCBIfam; TIGR00197; yjeF_nterm; 1.
DR   PANTHER; PTHR13232; NAD(P)H-HYDRATE EPIMERASE; 1.
DR   PANTHER; PTHR13232:SF12; YJEF N-TERMINAL DOMAIN-CONTAINING PROTEIN 3; 1.
DR   Pfam; PF03853; YjeF_N; 1.
DR   SUPFAM; SSF64153; YjeF N-terminal domain-like; 1.
DR   PROSITE; PS51385; YJEF_N; 1.
PE   1: Evidence at protein level;
KW   Alternative splicing; Lipid transport; Reference proteome; Transport.
FT   CHAIN           1..299
FT                   /note="YjeF N-terminal domain-containing protein 3"
FT                   /id="PRO_0000348461"
FT   DOMAIN          74..287
FT                   /note="YjeF N-terminal"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00719"
FT   VAR_SEQ         20..69
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|Ref.1"
FT                   /id="VSP_035170"
FT   VARIANT         213
FT                   /note="A -> T (in dbSNP:rs58031491)"
FT                   /id="VAR_061989"
FT   CONFLICT        293
FT                   /note="T -> A (in Ref. 4; BC020948)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   299 AA;  32585 MW;  5B708900DEBF6CCE CRC64;
     MSSAAGPDPS EAPEERHFLR ALELQPPLAD MGRAELSSNA TTSLVQRRKQ AWGRQSWLEQ
     IWNAGPVCQS TAEAAALERE LLEDYRFGRQ QLVELCGHAS AVAVTKAFPL PALSRKQRTV
     LVVCGPEQNG AVGLVCARHL RVFEYEPTIF YPTRSLDLLH RDLTTQCEKM DIPFLSYLPT
     EVQLINEAYG LVVDAVLGPG VEPGEVGGPC TRALATLKLL SIPLVSLDIP SGWDAETGSD
     SEDGLRPDVL VSLAAPKRCA GRFSGRHHFV AGRFVPDDVR RKFALRLPGY TGTDCVAAL
//
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