CKNB_CONIM
ID CKNB_CONIM Reviewed; 73 AA.
AC D0PX85; A0A125S9E3;
DT 16-MAY-2012, integrated into UniProtKB/Swiss-Prot.
DT 15-DEC-2009, sequence version 1.
DT 25-MAY-2022, entry version 22.
DE RecName: Full=Conotoxin im23b {ECO:0000303|PubMed:22399292};
DE AltName: Full=Conopeptide im009 {ECO:0000303|PubMed:30893765, ECO:0000312|EMBL:AME17667.1};
DE AltName: Full=Im23.2 {ECO:0000303|PubMed:22399292};
DE AltName: Full=U1-CTX-Ci1b;
DE Flags: Precursor;
OS Conus imperialis (Imperial cone).
OC Eukaryota; Metazoa; Spiralia; Lophotrochozoa; Mollusca; Gastropoda;
OC Caenogastropoda; Neogastropoda; Conoidea; Conidae; Conus; Stephanoconus.
OX NCBI_TaxID=35631;
RN [1]
RP NUCLEOTIDE SEQUENCE [MRNA], PARTIAL PROTEIN SEQUENCE, FUNCTION, DISULFIDE
RP BONDS, MASS SPECTROMETRY, AND SUBCELLULAR LOCATION.
RC TISSUE=Venom, and Venom duct;
RX PubMed=22399292; DOI=10.1074/jbc.m111.334615;
RA Ye M., Khoo K.K., Xu S., Zhou M., Boonyalai N., Perugini M.A., Shao X.,
RA Chi C., Galea C.A., Wang C., Norton R.S.;
RT "A helical conotoxin from Conus imperialis has a novel cysteine framework
RT and defines a new superfamily.";
RL J. Biol. Chem. 287:14973-14983(2012).
RN [2]
RP NUCLEOTIDE SEQUENCE [MRNA], IDENTIFICATION BY MASS SPECTROMETRY, AND
RP SUBCELLULAR LOCATION.
RC TISSUE=Venom, and Venom duct;
RX PubMed=30893765; DOI=10.3390/md17030177;
RA Jin A.H., Dutertre S., Dutt M., Lavergne V., Jones A., Lewis R.J.,
RA Alewood P.F.;
RT "Transcriptomic-proteomic correlation in the predation-evoked venom of the
RT cone snail, Conus imperialis.";
RL Mar. Drugs 17:0-0(2019).
CC -!- FUNCTION: Neurotoxin that induces excitatory symptoms in mice following
CC intracranial administration. No symptoms are observed after
CC intraperitoneal and intravenous (tail vein) injections.
CC {ECO:0000269|PubMed:22399292}.
CC -!- SUBCELLULAR LOCATION: Secreted {ECO:0000269|PubMed:22399292,
CC ECO:0000269|PubMed:30893765}.
CC -!- TISSUE SPECIFICITY: Expressed by the venom duct.
CC {ECO:0000305|PubMed:22399292, ECO:0000305|PubMed:30893765}.
CC -!- DOMAIN: The cysteine framework is XXIII (C-C-C-CC-C). {ECO:0000305}.
CC -!- MASS SPECTROMETRY: Mass=4874.0; Method=Unknown;
CC Evidence={ECO:0000269|PubMed:22399292};
CC -!- MISCELLANEOUS: Does not affect (up to 50 uM) the Nav1.7/SCN9A channel,
CC Drosophila Shaker channel and rat KCa1.1/KCNMA1 channel expressed in
CC HEK293 cell, as well as on whole cell current of neurons from neonatal
CC rat hippocampus and prefrontal cortex. In addition, no detectable
CC effect is observed on either action potential amplitude and duration or
CC Na(+) and Ca(2+) current amplitude and kinetics when im23a is tested on
CC action potentials and depolarization-activated Na(+) and Ca(2+)
CC currents in rat DRG neurons (PubMed:22399292).
CC {ECO:0000305|PubMed:22399292}.
CC -!- SIMILARITY: Belongs to the conotoxin K superfamily. {ECO:0000305}.
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DR EMBL; FJ375239; ACQ65999.1; -; mRNA.
DR EMBL; KT377403; AME17667.1; -; mRNA.
DR AlphaFoldDB; D0PX85; -.
DR SMR; D0PX85; -.
DR GO; GO:0005576; C:extracellular region; IEA:UniProtKB-SubCell.
DR GO; GO:0090729; F:toxin activity; IEA:UniProtKB-KW.
PE 1: Evidence at protein level;
KW Cleavage on pair of basic residues; Direct protein sequencing;
KW Disulfide bond; Neurotoxin; Secreted; Signal; Toxin.
FT SIGNAL 1..22
FT /evidence="ECO:0000255"
FT PROPEP 23..28
FT /evidence="ECO:0000305|PubMed:22399292"
FT /id="PRO_0000417033"
FT CHAIN 31..73
FT /note="Conotoxin im23b"
FT /evidence="ECO:0000269|PubMed:22399292"
FT /id="PRO_5000825650"
FT DISULFID 34..41
FT /evidence="ECO:0000250|UniProtKB:D0PX84"
FT DISULFID 45..55
FT /evidence="ECO:0000250|UniProtKB:D0PX84"
FT DISULFID 56..71
FT /evidence="ECO:0000250|UniProtKB:D0PX84"
SQ SEQUENCE 73 AA; 8091 MW; C61962220B1065B2 CRC64;
MIMRMTLTLF VLVVMTAASA SGDALTEAKR IPYCGQTGAE CYSWCIKQDL SKDWCCDFVK
TIARLPPAHI CSQ