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UNC7_CAEEL
ID   UNC7_CAEEL              Reviewed;         522 AA.
AC   Q03412;
DT   01-OCT-1993, integrated into UniProtKB/Swiss-Prot.
DT   01-OCT-1993, sequence version 1.
DT   03-AUG-2022, entry version 127.
DE   RecName: Full=Innexin unc-7;
DE   AltName: Full=Uncoordinated protein 7;
GN   Name=unc-7 {ECO:0000312|WormBase:R07D5.1a};
GN   Synonyms=unc-12 {ECO:0000312|WormBase:R07D5.1a},
GN   unc-124 {ECO:0000312|WormBase:R07D5.1a};
GN   ORFNames=R07D5.1 {ECO:0000312|WormBase:R07D5.1a};
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 [GENOMIC DNA], AND FUNCTION.
RC   STRAIN=Bristol N2;
RX   PubMed=7681023; DOI=10.1093/genetics/133.3.527;
RA   Starich T.A., Herman R.K., Shaw J.E.;
RT   "Molecular and genetic analysis of unc-7, a Caenorhabditis elegans gene
RT   required for coordinated locomotion.";
RL   Genetics 133:527-541(1993).
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 DISRUPTION PHENOTYPE.
RX   PubMed=17891142; DOI=10.1038/nn1981;
RA   Van Buskirk C., Sternberg P.W.;
RT   "Epidermal growth factor signaling induces behavioral quiescence in
RT   Caenorhabditis elegans.";
RL   Nat. Neurosci. 10:1300-1307(2007).
RN   [4]
RP   FUNCTION, TISSUE SPECIFICITY, AND MUTAGENESIS OF ALA-59; 216-GLN--ASP-522;
RP   PRO-224 AND CYS-238.
RX   PubMed=26156999; DOI=10.1523/jneurosci.0940-15.2015;
RA   Correa P.A., Gruninger T., Garcia L.R.;
RT   "DOP-2 D2-Like Receptor Regulates UNC-7 Innexins to Attenuate Recurrent
RT   Sensory Motor Neurons during C. elegans Copulation.";
RL   J. Neurosci. 35:9990-10004(2015).
CC   -!- FUNCTION: Structural component of the gap junctions (By similarity).
CC       Required for coordinated locomotion (PubMed:7681023). Probably by
CC       regulating neuronal transmission downstream of lin-3 and receptor lin-
CC       23 and phospholipase plc-3 in ALA neurons, involved in the decrease in
CC       pharyngeal pumping during the quiescent state that precedes each larval
CC       molt (PubMed:17891142). Plays a role in regulating male mating behavior
CC       by positively regulating inhibitory neuronal signaling transduction
CC       between chemosensory and mechanosensory neurons, and thus ensuring
CC       spicule insertion attempts are confined to the hermaphrodite vulva
CC       during copulation (PubMed:26156999). {ECO:0000250|UniProtKB:O61715,
CC       ECO:0000269|PubMed:17891142, ECO:0000269|PubMed:26156999,
CC       ECO:0000269|PubMed:7681023}.
CC   -!- SUBUNIT: Heterooligomer of unc-7 and unc-9. {ECO:0000305}.
CC   -!- SUBCELLULAR LOCATION: Cell membrane {ECO:0000305}; Multi-pass membrane
CC       protein {ECO:0000255|PROSITE-ProRule:PRU00351}. Cell junction, gap
CC       junction.
CC   -!- TISSUE SPECIFICITY: In hermaphrodites, expressed in all premotor and
CC       motor neurons, and in tail neurons (PubMed:26156999). In males,
CC       expressed in the anal depressor, gubernacular erector, gubernacular
CC       retractor and anterior oblique muscles, SPC, PCA, PCB, HOA, ray, head
CC       ganglion and ventral cord neurons (PubMed:26156999).
CC       {ECO:0000269|PubMed:26156999}.
CC   -!- DEVELOPMENTAL STAGE: Present in all developmental stages but most
CC       abundant in L1-L3 larvae.
CC   -!- DISRUPTION PHENOTYPE: Restores pharyngeal pumping but not impaired
CC       locomotion in 33 percent of animals overexpressing lin-3.
CC       {ECO:0000269|PubMed:17891142}.
CC   -!- SIMILARITY: Belongs to the pannexin family. {ECO:0000255|PROSITE-
CC       ProRule:PRU00351}.
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DR   EMBL; Z19122; CAA79529.1; -; Transcribed_RNA.
DR   EMBL; BX284606; CAA94607.1; -; Genomic_DNA.
DR   PIR; T24027; T24027.
DR   RefSeq; NP_001257255.1; NM_001270326.1.
DR   AlphaFoldDB; Q03412; -.
DR   SMR; Q03412; -.
DR   BioGRID; 46505; 2.
DR   STRING; 6239.R07D5.1a; -.
DR   TCDB; 1.A.25.1.2; the gap junction-forming innexin (innexin) family.
DR   EPD; Q03412; -.
DR   PaxDb; Q03412; -.
DR   EnsemblMetazoa; R07D5.1a.1; R07D5.1a.1; WBGene00006747.
DR   EnsemblMetazoa; R07D5.1a.2; R07D5.1a.2; WBGene00006747.
DR   GeneID; 181608; -.
DR   UCSC; R07D5.1; c. elegans.
DR   CTD; 181608; -.
DR   WormBase; R07D5.1a; CE06279; WBGene00006747; unc-7.
DR   eggNOG; ENOG502QVJ2; Eukaryota.
DR   InParanoid; Q03412; -.
DR   OMA; WHSGINL; -.
DR   PhylomeDB; Q03412; -.
DR   PRO; PR:Q03412; -.
DR   Proteomes; UP000001940; Chromosome X.
DR   Bgee; WBGene00006747; Expressed in pharyngeal muscle cell (C elegans) and 3 other tissues.
DR   ExpressionAtlas; Q03412; baseline and differential.
DR   GO; GO:0005911; C:cell-cell junction; IDA:WormBase.
DR   GO; GO:0005921; C:gap junction; IMP:UniProtKB.
DR   GO; GO:0016021; C:integral component of membrane; NAS:UniProtKB.
DR   GO; GO:0032589; C:neuron projection membrane; IDA:WormBase.
DR   GO; GO:0005886; C:plasma membrane; IDA:WormBase.
DR   GO; GO:0005243; F:gap junction channel activity; IDA:WormBase.
DR   GO; GO:0055077; F:gap junction hemi-channel activity; ISS:UniProtKB.
DR   GO; GO:1903351; P:cellular response to dopamine; IMP:UniProtKB.
DR   GO; GO:0016264; P:gap junction assembly; TAS:WormBase.
DR   GO; GO:0034220; P:ion transmembrane transport; IDA:WormBase.
DR   GO; GO:0040011; P:locomotion; IMP:UniProtKB.
DR   GO; GO:0018991; P:oviposition; IMP:WormBase.
DR   GO; GO:0090325; P:regulation of locomotion involved in locomotory behavior; IMP:UniProtKB.
DR   GO; GO:1902435; P:regulation of male mating behavior; IMP:UniProtKB.
DR   GO; GO:1902847; P:regulation of neuronal signal transduction; IMP:UniProtKB.
DR   GO; GO:0043051; P:regulation of pharyngeal pumping; IMP:WormBase.
DR   GO; GO:0072347; P:response to anesthetic; IGI:WormBase.
DR   GO; GO:0034609; P:spicule insertion; IMP:UniProtKB.
DR   InterPro; IPR000990; Innexin.
DR   PANTHER; PTHR11893; PTHR11893; 1.
DR   Pfam; PF00876; Innexin; 1.
DR   PRINTS; PR01262; INNEXIN.
DR   PROSITE; PS51013; PANNEXIN; 1.
PE   1: Evidence at protein level;
KW   Cell junction; Cell membrane; Gap junction; Ion channel; Ion transport;
KW   Membrane; Reference proteome; Transmembrane; Transmembrane helix;
KW   Transport.
FT   CHAIN           1..522
FT                   /note="Innexin unc-7"
FT                   /id="PRO_0000208517"
FT   TRANSMEM        151..171
FT                   /note="Helical"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00351"
FT   TRANSMEM        221..241
FT                   /note="Helical"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00351"
FT   TRANSMEM        320..340
FT                   /note="Helical"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00351"
FT   TRANSMEM        405..425
FT                   /note="Helical"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00351"
FT   REGION          1..67
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        14..30
FT                   /note="Pro residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        45..67
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   MUTAGEN         59
FT                   /note="A->T: In rg396; increases backwards movements.
FT                   Defects in male mating behavior with spicule protrusion
FT                   impairments. Impairs dopamine signaling."
FT                   /evidence="ECO:0000269|PubMed:26156999"
FT   MUTAGEN         216..522
FT                   /note="Missing: In e5; defects in male mating behavior with
FT                   spicule protrusion impairments. Impairs dopamine
FT                   signaling."
FT                   /evidence="ECO:0000269|PubMed:26156999"
FT   MUTAGEN         224
FT                   /note="P->L: In hs9; defects in male mating behavior with
FT                   spicule protrusion impairments. Impairs dopamine
FT                   signaling."
FT                   /evidence="ECO:0000269|PubMed:26156999"
FT   MUTAGEN         238
FT                   /note="C->Y: In hs10; defects in male mating behavior with
FT                   spicule protrusion impairments. Impairs dopamine
FT                   signaling."
FT                   /evidence="ECO:0000269|PubMed:26156999"
SQ   SEQUENCE   522 AA;  60121 MW;  950D7AFBA9F61120 CRC64;
     MLGSSSNPEP PLLSRIIGVP PPPPPRAPTT ALVLRVPTVD SPSKKKQQPD TRNKYQETAL
     RDKKTRTPLE KARHLDNLPS YQAQKLLDGS HQLRIDSHHV GSAGHGAGQG HGHKKEFGPA
     MILYYLASAF RALYPRLDDD FVDKLNYYYT TTILASFALL VSAKQYVGFP IQCWVPATFT
     DAMEQYTENY CWVQNTYWVP MQEDIPREIY SRRNRQIGYY QWVPFILAIE ALLFYVPCIL
     WRGLLYWHSG INLQGLVQMA CDARLMDSEI KTRTVYTMAR HMQDEVQLTN IDRQGHSRSC
     FSNLQLGANC GRHCGCYVTM LYIGIKVLYS ANVLLQFFLL NHLLGSNDLA YGFSLLKDLM
     HAIEWEQTGM FPRVTLCDFE VRVLGNIHRH TVQCVLMINM FNEKIFLFLW FWFLTCGIVT
     VCNTMYWILI MFIPSQGMSF VRKYLRVLPD HPAKPIADDV TLRKFTNNFL RKDGVFMLRM
     ISTHAGELMS SELILALWQD FNNVDRSPTQ FWDAEHGQGT ID
 
 
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