3SA5A_NAJSP
ID 3SA5A_NAJSP Reviewed; 81 AA.
AC O73857;
DT 02-FEB-2004, integrated into UniProtKB/Swiss-Prot.
DT 02-FEB-2004, sequence version 2.
DT 03-AUG-2022, entry version 83.
DE RecName: Full=Cytotoxin 5a;
DE AltName: Full=Cardiotoxin 5a;
DE Short=CTX-5a;
DE Short=Ctx5a;
DE Flags: Precursor;
OS Naja sputatrix (Malayan spitting cobra) (Naja naja sputatrix).
OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
OC Lepidosauria; Squamata; Bifurcata; Unidentata; Episquamata; Toxicofera;
OC Serpentes; Colubroidea; Elapidae; Elapinae; Naja.
OX NCBI_TaxID=33626;
RN [1]
RP NUCLEOTIDE SEQUENCE [MRNA], PROTEIN SEQUENCE OF 22-71, AND SUBCELLULAR
RP LOCATION.
RC TISSUE=Venom, and Venom gland;
RX PubMed=9565688; DOI=10.1016/s0304-4165(97)00143-8;
RA Jeyaseelan K., Armugam A., Lachumanan R., Tan C.H., Tan N.H.;
RT "Six isoforms of cardiotoxin in malayan spitting cobra (Naja naja
RT sputatrix) venom: cloning and characterization of cDNAs.";
RL Biochim. Biophys. Acta 1380:209-222(1998).
RN [2]
RP NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 20-81.
RC TISSUE=Liver;
RX PubMed=9738945; DOI=10.1016/s0014-5793(98)00894-1;
RA Lachumanan R., Armugam A., Tan C.H., Jeyaseelan K.;
RT "Structure and organization of the cardiotoxin genes in Naja naja
RT sputatrix.";
RL FEBS Lett. 433:119-124(1998).
CC -!- FUNCTION: Shows cytolytic activity on many different cells by forming
CC pore in lipid membranes. In vivo, increases heart rate or kills the
CC animal by cardiac arrest. In addition, it binds to heparin with high
CC affinity, interacts with Kv channel-interacting protein 1 (KCNIP1) in a
CC calcium-independent manner, and binds to integrin alpha-V/beta-3
CC (ITGAV/ITGB3) with moderate affinity. {ECO:0000250|UniProtKB:P60301,
CC ECO:0000250|UniProtKB:P60304}.
CC -!- SUBUNIT: Monomer in solution; Homodimer and oligomer in the presence of
CC negatively charged lipids forming a pore with a size ranging between 20
CC and 30 Angstroms. {ECO:0000250|UniProtKB:P60301}.
CC -!- SUBCELLULAR LOCATION: Secreted {ECO:0000269|PubMed:9565688}. Target
CC cell membrane {ECO:0000250|UniProtKB:P60301}.
CC -!- TISSUE SPECIFICITY: Expressed by the venom gland. {ECO:0000305}.
CC -!- MISCELLANEOUS: Is classified as a S-type cytotoxin, since a serine
CC residue stands at position 49 (Ser-29 in standard classification).
CC {ECO:0000305}.
CC -!- SIMILARITY: Belongs to the snake three-finger toxin family. Short-chain
CC subfamily. Type IA cytotoxin sub-subfamily. {ECO:0000305}.
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DR EMBL; U86596; AAC27691.1; -; mRNA.
DR EMBL; AF064099; AAC61317.1; -; Genomic_DNA.
DR AlphaFoldDB; O73857; -.
DR SMR; O73857; -.
DR PRIDE; O73857; -.
DR GO; GO:0005576; C:extracellular region; IEA:UniProtKB-SubCell.
DR GO; GO:0016020; C:membrane; IEA:UniProtKB-KW.
DR GO; GO:0090729; F:toxin activity; IEA:UniProtKB-KW.
DR GO; GO:0019835; P:cytolysis; IEA:UniProtKB-KW.
DR CDD; cd00206; snake_toxin; 1.
DR Gene3D; 2.10.60.10; -; 1.
DR InterPro; IPR003572; Cytotoxin_Cobra.
DR InterPro; IPR003571; Snake_3FTx.
DR InterPro; IPR045860; Snake_toxin-like_sf.
DR InterPro; IPR018354; Snake_toxin_con_site.
DR PRINTS; PR00282; CYTOTOXIN.
DR SUPFAM; SSF57302; SSF57302; 1.
DR PROSITE; PS00272; SNAKE_TOXIN; 1.
PE 1: Evidence at protein level;
KW Cardiotoxin; Cytolysis; Direct protein sequencing; Disulfide bond;
KW Membrane; Secreted; Signal; Target cell membrane; Target membrane; Toxin.
FT SIGNAL 1..21
FT /evidence="ECO:0000269|PubMed:9565688"
FT CHAIN 22..81
FT /note="Cytotoxin 5a"
FT /evidence="ECO:0000305|PubMed:9565688"
FT /id="PRO_0000035400"
FT DISULFID 24..42
FT /evidence="ECO:0000250|UniProtKB:P60301"
FT DISULFID 35..59
FT /evidence="ECO:0000250|UniProtKB:P60301"
FT DISULFID 63..74
FT /evidence="ECO:0000250|UniProtKB:P60301"
FT DISULFID 75..80
FT /evidence="ECO:0000250|UniProtKB:P60301"
SQ SEQUENCE 81 AA; 9041 MW; 182274E2FAD949BA CRC64;
MKTLLLTLVV VTIVCLDLGY TLKCNKLVPL FYKTCPAGKN LCYKMFMVSN LTVPVKRGCI
DVCPKNSALV KYVCCNTDRC N