位置:首页 > 蛋白库 > UNC3_CAEEL
UNC3_CAEEL
ID   UNC3_CAEEL              Reviewed;         491 AA.
AC   Q93705; K8FE05; O61576;
DT   30-MAY-2000, integrated into UniProtKB/Swiss-Prot.
DT   27-MAY-2002, sequence version 3.
DT   03-AUG-2022, entry version 155.
DE   RecName: Full=Transcription factor unc-3;
DE   AltName: Full=Uncoordinated protein 3;
DE            Short=CEO/E;
GN   Name=unc-3; ORFNames=Y16B4A.1;
OS   Caenorhabditis elegans.
OC   Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida;
OC   Rhabditina; Rhabditomorpha; Rhabditoidea; Rhabditidae; Peloderinae;
OC   Caenorhabditis.
OX   NCBI_TaxID=6239;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, DEVELOPMENTAL STAGE, AND DISRUPTION
RP   PHENOTYPE.
RC   STRAIN=Bristol N2;
RX   PubMed=9502737; DOI=10.1242/dev.125.8.1561;
RA   Prasad B.C., Ye B., Zackhary R., Schrader K., Seydoux G., Reed R.R.;
RT   "unc-3, a gene required for axonal guidance in Caenorhabditis elegans,
RT   encodes a member of the O/E family of transcription factors.";
RL   Development 125:1561-1568(1998).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=Bristol N2;
RX   PubMed=9851916; DOI=10.1126/science.282.5396.2012;
RG   The C. elegans sequencing consortium;
RT   "Genome sequence of the nematode C. elegans: a platform for investigating
RT   biology.";
RL   Science 282:2012-2018(1998).
RN   [3]
RP   FUNCTION, AND INTERACTION WITH JMJD-3.1.
RX   PubMed=25124442; DOI=10.1126/science.1255885;
RA   Zuryn S., Ahier A., Portoso M., White E.R., Morin M.C., Margueron R.,
RA   Jarriault S.;
RT   "Sequential histone-modifying activities determine the robustness of
RT   transdifferentiation.";
RL   Science 345:826-829(2014).
RN   [4]
RP   FUNCTION, AND MUTAGENESIS OF 309-TRP--SER-491.
RX   PubMed=28056346; DOI=10.1016/j.neuron.2016.11.036;
RA   Kerk S.Y., Kratsios P., Hart M., Mourao R., Hobert O.;
RT   "Diversification of C. elegans Motor Neuron Identity via Selective Effector
RT   Gene Repression.";
RL   Neuron 93:80-98(2017).
CC   -!- FUNCTION: Transcription factor (PubMed:28056346). Involved in motor
CC       neuron fate determination and maintenance, acting as an activator of
CC       gene expression in a subset of motor neurons (PubMed:28056346).
CC       Required to maintain the expression of transcriptional repressors bnc-1
CC       and cfi-1, which play roles in the cell fate of motor neurons
CC       (PubMed:28056346). May play a role in the expression of proteins
CC       essential for axonal pathfinding and/or neuronal differentiation in
CC       both sensory and motor neurons (PubMed:9502737). Cooperates with jmjd-
CC       3.1 and wdr-5.1 to ensure robust transdifferentiation of the Y rectal
CC       cell to the PDA motor neuron during larval development
CC       (PubMed:25124442). {ECO:0000269|PubMed:25124442,
CC       ECO:0000269|PubMed:28056346, ECO:0000269|PubMed:9502737}.
CC   -!- SUBUNIT: Interacts with jmjd-3.1. {ECO:0000269|PubMed:25124442}.
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000305}.
CC   -!- DEVELOPMENTAL STAGE: Expressed in certain chemosensory neurons (ASI
CC       amphid neurons) throughout development and is also expressed
CC       transiently in developing motor neurons when these cells undergo axonal
CC       outgrowth. {ECO:0000269|PubMed:9502737}.
CC   -!- DISRUPTION PHENOTYPE: Worms show defects in the axonal outgrowth of
CC       motor neurons, as well as defects in dauer formation, a process
CC       requiring chemosensory inputs. {ECO:0000269|PubMed:9502737}.
CC   -!- SIMILARITY: Belongs to the COE family. {ECO:0000305}.
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; AF052060; AAC06226.1; -; mRNA.
DR   EMBL; AL023825; CCO25892.1; -; Genomic_DNA.
DR   EMBL; Z81081; CCO25892.1; JOINED; Genomic_DNA.
DR   PIR; T22089; T22089.
DR   PIR; T42991; T42991.
DR   RefSeq; NP_510453.1; NM_078052.3.
DR   AlphaFoldDB; Q93705; -.
DR   SMR; Q93705; -.
DR   BioGRID; 46470; 6.
DR   DIP; DIP-61432N; -.
DR   IntAct; Q93705; 1.
DR   STRING; 6239.Y16B4A.1; -.
DR   EPD; Q93705; -.
DR   PaxDb; Q93705; -.
DR   EnsemblMetazoa; Y16B4A.1.1; Y16B4A.1.1; WBGene00006743.
DR   GeneID; 181573; -.
DR   KEGG; cel:CELE_Y16B4A.1; -.
DR   UCSC; Y16B4A.1; c. elegans.
DR   CTD; 181573; -.
DR   WormBase; Y16B4A.1; CE29366; WBGene00006743; unc-3.
DR   eggNOG; KOG3836; Eukaryota.
DR   GeneTree; ENSGT00950000182859; -.
DR   HOGENOM; CLU_016320_0_0_1; -.
DR   InParanoid; Q93705; -.
DR   OMA; LCPSEGW; -.
DR   OrthoDB; 817293at2759; -.
DR   PhylomeDB; Q93705; -.
DR   PRO; PR:Q93705; -.
DR   Proteomes; UP000001940; Chromosome X.
DR   Bgee; WBGene00006743; Expressed in pharyngeal muscle cell (C elegans) and 3 other tissues.
DR   GO; GO:0005634; C:nucleus; IDA:WormBase.
DR   GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; IBA:GO_Central.
DR   GO; GO:0035035; F:histone acetyltransferase binding; IPI:WormBase.
DR   GO; GO:0042802; F:identical protein binding; IDA:WormBase.
DR   GO; GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
DR   GO; GO:0000978; F:RNA polymerase II cis-regulatory region sequence-specific DNA binding; IBA:GO_Central.
DR   GO; GO:0000977; F:RNA polymerase II transcription regulatory region sequence-specific DNA binding; IDA:WormBase.
DR   GO; GO:0007411; P:axon guidance; IMP:UniProtKB.
DR   GO; GO:0040024; P:dauer larval development; IGI:WormBase.
DR   GO; GO:0043065; P:positive regulation of apoptotic process; IMP:WormBase.
DR   GO; GO:0045944; P:positive regulation of transcription by RNA polymerase II; IMP:WormBase.
DR   GO; GO:0010975; P:regulation of neuron projection development; IMP:WormBase.
DR   GO; GO:0006357; P:regulation of transcription by RNA polymerase II; IBA:GO_Central.
DR   CDD; cd11606; COE_DBD; 1.
DR   CDD; cd01175; IPT_COE; 1.
DR   Gene3D; 2.60.40.10; -; 1.
DR   Gene3D; 2.60.40.3180; -; 1.
DR   InterPro; IPR032200; COE_DBD.
DR   InterPro; IPR038173; COE_DBD_sf.
DR   InterPro; IPR032201; COE_HLH.
DR   InterPro; IPR038006; COE_IPT.
DR   InterPro; IPR013783; Ig-like_fold.
DR   InterPro; IPR014756; Ig_E-set.
DR   InterPro; IPR002909; IPT_dom.
DR   InterPro; IPR003523; Transcription_factor_COE.
DR   InterPro; IPR018350; Transcription_factor_COE_CS.
DR   PANTHER; PTHR10747; PTHR10747; 1.
DR   Pfam; PF16422; COE1_DBD; 1.
DR   Pfam; PF16423; COE1_HLH; 1.
DR   Pfam; PF01833; TIG; 1.
DR   SMART; SM00429; IPT; 1.
DR   SUPFAM; SSF81296; SSF81296; 1.
DR   PROSITE; PS01345; COE; 1.
PE   1: Evidence at protein level;
KW   Developmental protein; DNA-binding; Metal-binding; Nucleus;
KW   Reference proteome; Transcription; Transcription regulation; Zinc;
KW   Zinc-finger.
FT   CHAIN           1..491
FT                   /note="Transcription factor unc-3"
FT                   /id="PRO_0000107824"
FT   DOMAIN          269..355
FT                   /note="IPT/TIG"
FT                   /evidence="ECO:0000255"
FT   ZN_FING         154..173
FT                   /note="C5-type"
FT                   /evidence="ECO:0000255"
FT   REGION          66..69
FT                   /note="Interaction with DNA"
FT                   /evidence="ECO:0000250|UniProtKB:Q07802"
FT   REGION          200..207
FT                   /note="Interaction with DNA"
FT                   /evidence="ECO:0000250|UniProtKB:Q07802"
FT   REGION          239..242
FT                   /note="Interaction with DNA"
FT                   /evidence="ECO:0000250|UniProtKB:Q07802"
FT   REGION          240..261
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   SITE            166
FT                   /note="Interaction with DNA"
FT                   /evidence="ECO:0000250|UniProtKB:Q07802"
FT   SITE            175
FT                   /note="Interaction with DNA"
FT                   /evidence="ECO:0000250|UniProtKB:Q07802"
FT   MUTAGEN         309..491
FT                   /note="Missing: In e151; drastically reduces expression of
FT                   acetylcholine receptor genes acr-5 and acr-16. In a bnc-1
FT                   mutant background, abolishes expression of the BMP-like
FT                   protein unc-129 in DA and DB motor neurons (MNs);
FT                   furthermore, ectopic expression of unc-129 in VA and VB MNs
FT                   is also lost. In a mab-9 mutant background, ectopic
FT                   expression of Degenerin del-1 gene in DA and DB MNs is
FT                   abolished."
FT                   /evidence="ECO:0000269|PubMed:28056346"
SQ   SEQUENCE   491 AA;  55001 MW;  CFC71C132D02D485 CRC64;
     MSLTAPLRAG QMNFYDEPYN PVLNLHIQPS VKDENQRSTW PIIDTSNTST QIARAHFEKH
     PPNNLRKSNF FHFVIALYDR NSQPIEVERT QFAGFVEKEK EVDGQDTRNG IHYRLSLMFQ
     NGIRSEHDLF VRLIDSSTKQ AITYEGQDKN PEMCRVLLTH EVMCSRCCEK KSCGNRNETP
     SDPVIIDRFF LKFFLKCNQN CLKNAGNPRD MRRFQVVLCS SARIDGPLLA VSDNMFVHNN
     SKHGRRTKRT DASDDSEYSE SAELPSSVPV IKALFPSEGW IQGGTQVVLI GENFFEGLQV
     AFGTASPNWG ESVQLISPHA IRVTTPPKHS AGPVDVTLQY KSKTYSRGTP LRFSYITLAE
     PGIEYGFQRL QKLLPKYPGD PERLPKDQIL KRAAELAEAL YNRTSTESLS SYYHTQFDAT
     SDYAARTHTS PRSTLPYGAG PPALSSAVYQ TSYPTVNATP AANFLNTQTG FATFGAVNPF
     AATLQSSSRL S
 
 
维奥蛋白资源库 - 中文蛋白资源 CopyRight © 2010-2024