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PDBsum entry 1umr
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Sugar binding protein
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PDB id
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1umr
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Contents |
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* Residue conservation analysis
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PDB id:
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Sugar binding protein
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Title:
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Crystal structure of the platelet activator convulxin, a disulfide linked a4b4 cyclic tetramer from the venom of crotalus durissus terrificus
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Structure:
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Convulxin alpha. Chain: a, b. Synonym: cvx alpha. Convulxin beta. Chain: c, d. Synonym: cvx beta
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Source:
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Crotalus durissus terrificus. South american rattlesnake. Organism_taxid: 8732. Tissue: venom gland. Tissue: venom gland
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Biol. unit:
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Octamer (from PDB file)
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Resolution:
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2.40Å
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R-factor:
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0.190
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R-free:
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0.264
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Authors:
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M.T.Murakami,S.P.Zela,L.M.Gava,S.Michelan-Duarte,A.C.O.Cintra, R.K.Arni
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Key ref:
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M.T.Murakami
et al.
(2003).
Crystal structure of the platelet activator convulxin, a disulfide-linked alpha4beta4 cyclic tetramer from the venom of Crotalus durissus terrificus.
Biochem Biophys Res Commun,
310,
478-482.
PubMed id:
DOI:
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Date:
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28-Aug-03
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Release date:
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21-Nov-03
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PROCHECK
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Headers
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References
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DOI no:
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Biochem Biophys Res Commun
310:478-482
(2003)
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PubMed id:
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Crystal structure of the platelet activator convulxin, a disulfide-linked alpha4beta4 cyclic tetramer from the venom of Crotalus durissus terrificus.
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M.T.Murakami,
S.P.Zela,
L.M.Gava,
S.Michelan-Duarte,
A.C.Cintra,
R.K.Arni.
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ABSTRACT
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Convulxin (CVX), a C-type lectin, isolated from the venom of the South American
rattlesnake Crotalus durissus terrificus, causes cardiovascular and respiratory
disturbances and is a potent platelet activator which binds to platelet
glycoprotein GPVI. The structure of CVX has been solved at 2.4A resolution to a
crystallographic residual of 18.6% (R(free)=26.4%). CVX is a disulfide linked
heterodimer consisting of homologous alpha and beta chains. The heterodimers are
additionally linked by disulfide bridges to form cyclic
alpha(4)beta(4)heterotetramers. These domains exhibit significant homology to
the carbohydrate-binding domains of C-type lectins, to the factor IX-binding
protein (IX-bp), and to flavocetin-A (Fl-A) but sequence and structural
differences are observed in both the domains in the putative Ca(2+)and
carbohydrate binding regions.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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T.Sajevic,
A.Leonardi,
and
I.Križaj
(2011).
Haemostatically active proteins in snake venoms.
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Toxicon,
57,
627-645.
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R.Doley,
and
R.M.Kini
(2009).
Protein complexes in snake venom.
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Cell Mol Life Sci,
66,
2851-2871.
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E.Hooley,
E.Papagrigoriou,
A.Navdaev,
A.V.Pandey,
J.M.Clemetson,
K.J.Clemetson,
and
J.Emsley
(2008).
The crystal structure of the platelet activator aggretin reveals a novel (alphabeta)2 dimeric structure.
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Biochemistry,
47,
7831-7837.
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PDB code:
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M.G.Tomlinson,
S.D.Calaminus,
O.Berlanga,
J.M.Auger,
T.Bori-Sanz,
L.Meyaard,
and
S.P.Watson
(2007).
Collagen promotes sustained glycoprotein VI signaling in platelets and cell lines.
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J Thromb Haemost,
5,
2274-2283.
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K.Kato,
K.Furihata,
Y.Cheli,
G.Radis-Baptista,
and
T.J.Kunicki
(2006).
Effect of multimer size and a natural dimorphism on the binding of convulxin to platelet glycoprotein (GP)VI.
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J Thromb Haemost,
4,
1107-1113.
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A.Bazaa,
N.Marrakchi,
M.El Ayeb,
L.Sanz,
and
J.J.Calvete
(2005).
Snake venomics: comparative analysis of the venom proteomes of the Tunisian snakes Cerastes cerastes, Cerastes vipera and Macrovipera lebetina.
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Proteomics,
5,
4223-4235.
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G.Xu,
Q.Huang,
M.Teng,
P.Liu,
Y.Dong,
and
L.Niu
(2005).
Crystallization and preliminary X-ray crystallographic analysis of agkicetin-C from Deinagkistrodon acutus venom.
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Acta Crystallogr Sect F Struct Biol Cryst Commun,
61,
75-78.
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G.Xu,
M.Teng,
L.Niu,
P.Liu,
Y.Dong,
Q.Liu,
Q.Huang,
and
Q.Hao
(2004).
Purification, characterization, crystallization and preliminary X-ray crystallographic analysis of two novel C-type lectin-like proteins: Aall-A and Aall-B from Deinagkistrodon acutus venom.
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Acta Crystallogr D Biol Crystallogr,
60,
2035-2037.
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T.Batuwangala,
M.Leduc,
J.M.Gibbins,
C.Bon,
and
E.Y.Jones
(2004).
Structure of the snake-venom toxin convulxin.
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Acta Crystallogr D Biol Crystallogr,
60,
46-53.
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PDB code:
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
code is
shown on the right.
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