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SEU1_CAEEL
ID   SEU1_CAEEL              Reviewed;         672 AA.
AC   A9D2P7; H2L0L8; H2L0L9; Q8IU02; V6CLR5;
DT   29-SEP-2021, integrated into UniProtKB/Swiss-Prot.
DT   05-FEB-2008, sequence version 1.
DT   03-AUG-2022, entry version 81.
DE   RecName: Full=Protein seu-1 {ECO:0000305};
DE   AltName: Full=Suppressor of ectopic unc-5 {ECO:0000312|WormBase:Y73B6BL.5d};
GN   Name=seu-1 {ECO:0000312|WormBase:Y73B6BL.5d};
GN   ORFNames=Y73B6BL.5 {ECO:0000312|WormBase:Y73B6BL.5d};
OS   Caenorhabditis elegans.
OC   Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida;
OC   Rhabditina; Rhabditomorpha; Rhabditoidea; Rhabditidae; Peloderinae;
OC   Caenorhabditis.
OX   NCBI_TaxID=6239 {ECO:0000312|Proteomes:UP000001940};
RN   [1] {ECO:0000312|Proteomes:UP000001940}
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=Bristol N2 {ECO:0000312|Proteomes:UP000001940};
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   [2] {ECO:0000305}
RP   FUNCTION, AND MUTAGENESIS OF 191-ARG--LEU-672.
RX   PubMed=9473333; DOI=10.1006/dbio.1997.8790;
RA   Colavita A., Culotti J.G.;
RT   "Suppressors of ectopic UNC-5 growth cone steering identify eight genes
RT   involved in axon guidance in Caenorhabditis elegans.";
RL   Dev. Biol. 194:72-85(1998).
RN   [3] {ECO:0000305}
RP   FUNCTION, SUBCELLULAR LOCATION, TISSUE SPECIFICITY, DEVELOPMENTAL STAGE,
RP   AND MUTAGENESIS OF 191-ARG--LEU-672 AND 630-GLN--LEU-672.
RX   PubMed=17716643; DOI=10.1016/j.ydbio.2007.07.014;
RA   Zheng H., Coudiere L., Camia C., Colavita A., Culotti J.G., Merz D.C.;
RT   "C. elegans seu-1 encodes novel nuclear proteins that regulate responses to
RT   UNC-6/netrin guidance cues.";
RL   Dev. Biol. 310:44-53(2007).
CC   -!- FUNCTION: Together with unc-5, involved in touch neuron axon guidance
CC       (PubMed:9473333). During gonad morphogenesis, plays a role in the unc-
CC       5-/unc-6-mediated migration of distal tip cells along the body
CC       (PubMed:17716643). {ECO:0000269|PubMed:17716643,
CC       ECO:0000269|PubMed:9473333}.
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000269|PubMed:17716643}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=5;
CC       Name=d {ECO:0000312|WormBase:Y73B6BL.5d}; Synonyms=seu-1A
CC       {ECO:0000303|PubMed:17716643};
CC         IsoId=A9D2P7-1; Sequence=Displayed;
CC       Name=a {ECO:0000312|WormBase:Y73B6BL.5a}; Synonyms=seu-1B
CC       {ECO:0000303|PubMed:17716643};
CC         IsoId=A9D2P7-2; Sequence=VSP_061194, VSP_061195;
CC       Name=b {ECO:0000312|WormBase:Y73B6BL.5b};
CC         IsoId=A9D2P7-3; Sequence=VSP_061193, VSP_061194, VSP_061195;
CC       Name=c {ECO:0000312|WormBase:Y73B6BL.5c};
CC         IsoId=A9D2P7-4; Sequence=VSP_061192, VSP_061194, VSP_061195;
CC       Name=e {ECO:0000312|WormBase:Y73B6BL.5e};
CC         IsoId=A9D2P7-5; Sequence=VSP_061192, VSP_061195;
CC   -!- TISSUE SPECIFICITY: Highly expressed in intestinal cells, lateral
CC       hypodermal (seam) cells, Pn.p ventral hypodermal cells, and spermatheca
CC       (PubMed:17716643). Expressed at low levels in the ventral nerve cord
CC       (PubMed:17716643). {ECO:0000269|PubMed:17716643}.
CC   -!- DEVELOPMENTAL STAGE: Expressed in all nuclei in the early embryo until
CC       the comma stage, and then is expressed in body wall muscle cells and
CC       pharynx in the embryo (PubMed:17716643). Expressed in muscle until the
CC       late larval stages (PubMed:17716643). In larvae, highly expressed in
CC       intestinal cells, lateral hypodermal (seam) cells, Pn.p ventral
CC       hypodermal cells, and spermatheca (PubMed:17716643). In L3 stage
CC       larvae, expressed at low levels in distal tip cells during the ventral-
CC       to-dorsal second and longitudinal third migration phases, but not
CC       expressed during the first migration phase (PubMed:17716643). In L4
CC       stage larvae, expressed at low levels in the ventral nerve cord
CC       (PubMed:17716643). {ECO:0000269|PubMed:17716643}.
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DR   EMBL; BX284604; CCD74152.1; -; Genomic_DNA.
DR   EMBL; BX284604; CCD74153.1; -; Genomic_DNA.
DR   EMBL; BX284604; CCD74154.1; -; Genomic_DNA.
DR   EMBL; BX284604; CCD74193.1; -; Genomic_DNA.
DR   EMBL; BX284604; CDK13502.1; -; Genomic_DNA.
DR   RefSeq; NP_001293775.1; NM_001306846.1.
DR   RefSeq; NP_500965.1; NM_068564.4. [A9D2P7-2]
DR   RefSeq; NP_500966.1; NM_068565.5. [A9D2P7-3]
DR   RefSeq; NP_741420.1; NM_171358.3.
DR   RefSeq; NP_741421.2; NM_171359.3. [A9D2P7-1]
DR   AlphaFoldDB; A9D2P7; -.
DR   STRING; 6239.Y73B6BL.5d.2; -.
DR   EPD; A9D2P7; -.
DR   PaxDb; A9D2P7; -.
DR   EnsemblMetazoa; Y73B6BL.5a.1; Y73B6BL.5a.1; WBGene00004783. [A9D2P7-2]
DR   EnsemblMetazoa; Y73B6BL.5b.1; Y73B6BL.5b.1; WBGene00004783. [A9D2P7-3]
DR   EnsemblMetazoa; Y73B6BL.5c.1; Y73B6BL.5c.1; WBGene00004783. [A9D2P7-4]
DR   EnsemblMetazoa; Y73B6BL.5d.1; Y73B6BL.5d.1; WBGene00004783. [A9D2P7-1]
DR   EnsemblMetazoa; Y73B6BL.5e.1; Y73B6BL.5e.1; WBGene00004783. [A9D2P7-5]
DR   GeneID; 177394; -.
DR   KEGG; cel:CELE_Y73B6BL.5; -.
DR   UCSC; Y73B6BL.5d.1; c. elegans.
DR   CTD; 177394; -.
DR   WormBase; Y73B6BL.5a; CE29147; WBGene00004783; seu-1. [A9D2P7-2]
DR   WormBase; Y73B6BL.5b; CE29148; WBGene00004783; seu-1. [A9D2P7-3]
DR   WormBase; Y73B6BL.5c; CE31129; WBGene00004783; seu-1. [A9D2P7-4]
DR   WormBase; Y73B6BL.5d; CE41963; WBGene00004783; seu-1. [A9D2P7-1]
DR   WormBase; Y73B6BL.5e; CE49209; WBGene00004783; seu-1. [A9D2P7-5]
DR   eggNOG; ENOG502TGB7; Eukaryota.
DR   HOGENOM; CLU_028920_0_0_1; -.
DR   InParanoid; A9D2P7; -.
DR   OMA; WCALLAC; -.
DR   OrthoDB; 1799806at2759; -.
DR   Proteomes; UP000001940; Chromosome IV.
DR   Bgee; WBGene00004783; Expressed in embryo and 3 other tissues.
DR   ExpressionAtlas; A9D2P7; baseline and differential.
DR   GO; GO:0005634; C:nucleus; IDA:WormBase.
DR   GO; GO:0033563; P:dorsal/ventral axon guidance; IGI:WormBase.
DR   GO; GO:0040011; P:locomotion; IMP:WormBase.
PE   1: Evidence at protein level;
KW   Alternative splicing; Nucleus; Reference proteome.
FT   CHAIN           1..672
FT                   /note="Protein seu-1"
FT                   /id="PRO_0000453731"
FT   REGION          1..463
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          576..672
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        59..84
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        85..106
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        107..140
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        190..272
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        287..305
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        324..339
FT                   /note="Acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        340..358
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        370..449
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        609..660
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VAR_SEQ         1..180
FT                   /note="Missing (in isoform c and isoform e)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_061192"
FT   VAR_SEQ         88..132
FT                   /note="Missing (in isoform b)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_061193"
FT   VAR_SEQ         461..576
FT                   /note="Missing (in isoform a, isoform b and isoform c)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_061194"
FT   VAR_SEQ         665..672
FT                   /note="VSLSLKHL -> RRRPSPPRGRPGEKVVQSYRNGV (in isoform a,
FT                   isoform b, isoform c and isoform e)"
FT                   /evidence="ECO:0000305"
FT                   /id="VSP_061195"
FT   MUTAGEN         191..672
FT                   /note="Missing: In ev520; mild uncoordinated phenotype.
FT                   Causes no axon guidance defects or distal tip cell
FT                   migrations and gonad morphology defects. Enhances the
FT                   distal tip cell migration defects of unc-5 ev585, unc-5 e53
FT                   or unc-6 ev400 mutants. Suppresses the anterior touch
FT                   neuron axon guidance defects in an unc-5 over-expression
FT                   mutant background."
FT                   /evidence="ECO:0000269|PubMed:17716643,
FT                   ECO:0000269|PubMed:9473333"
FT   MUTAGEN         630..672
FT                   /note="Missing: In ev529; causes no distal tip cell
FT                   migrations and gonad morphology defects. Enhances the
FT                   distal tip cell migration defects of the unc-5 ev585, unc-5
FT                   e53 or unc-6 ev400 mutants."
FT                   /evidence="ECO:0000269|PubMed:17716643"
SQ   SEQUENCE   672 AA;  75388 MW;  E69F422D91F7C5A8 CRC64;
     MSSIRNQNDN RRPTFRDHRT PQFSGRGGSG GGGRRLQNPA HYPQRRDMSP IRRSSAISPV
     RRSQDHRQRS PEVRRHRSPE KESKDAVVTS TGSSRGATSA SVTSSSRRHE SGERHRETHR
     REDKEKKPEK STDRDADRSN NIAARIQAPV VSSSTHHHHS NRHENRKSTA VKRPAADNRP
     MTYSTDVSVS RHSENRRKSS SDVSRRHGDK EKRDRKREDV KKKSNGERSS SSGRRREEDH
     KRKSESSRKE KKDEDVKEKV VDENKVEDEA VEMQGLVEVD CCEEEETIEQ AKEHGSDEPE
     RPESHQSAHS AAVSNASHHS DSEEELDYEE DDIDVDLDGD IDVETMKMAA RGDLKVDDTT
     DEDEINDVKD ETMEEQKEDG EPEKKKPRTS ENDDKDKKHH GSSSSNSHRR REDDKDRRQS
     SDHHKERRRS PATRQRATDH KESRRSEGTS TRVESAASAA GTEIQRIPSL LTMRIAAPPG
     IKKLETLYHS GSGGSSSSSS HSSEMIIVGE TFSNRWCQCS CAHHLPTTSS AAAAAGSLDA
     SPASSSSSSS NSDASVSRIP SLMSLRTPFN NSCLFLAPPP PPSSSSSSKR SHEAAARIRA
     PSPPRRSFGD RGNRSDEHHG GSRHMDVGPQ RRRLQDHRVR DDGRRVSSFE DRKRPERGFQ
     DSGRVSLSLK HL
 
 
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