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PDBsum entry 1tgx
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* Residue conservation analysis
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J Mol Biol
239:122-136
(1994)
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PubMed id:
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X-ray structure at 1.55 A of toxin gamma, a cardiotoxin from Naja nigricollis venom. Crystal packing reveals a model for insertion into membranes.
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A.Bilwes,
B.Rees,
D.Moras,
R.Ménez,
A.Ménez.
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ABSTRACT
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The crystal structure of toxin gamma from Naja nigricollis has been solved and
refined to 1.55 A resolution. The final R-factor, computed with all X-ray data
available, is 17.9%. The three-dimensional structure is characterized by a core
formed by two beta-sheets organized in three extended loops. It is similar to
that of cardiotoxin V4II from Naja mossambica mossambica, with the exception of
the hydrophobic loop I. The flexibility and variability of the loops contrast
sharply with the rigidity of the molecular core and its high degree of
structural conservation among the cardiotoxin family. The most flexible loop II
adopts different conformations in the three monomers forming the crystal
asymmetric unit. These monomers form a trimer around an approximate 3-fold axis,
with conserved hydrophobic side-chains on the outside and hydrophilic residues
in the central channel or involved in interactions with the other molecules. The
trimer thus resembles a membrane protein with a central channel that could allow
the passage of small ions. It is proposed as a model for the insertion of
cardiotoxin into a membrane.
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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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S.S.Hasson,
A.A.Al-Jabri,
T.A.Sallam,
M.S.Al-Balushi,
and
R.A.Mothana
(2010).
Antisnake Venom Activity of Hibiscus aethiopicus L. against Echis ocellatus and Naja n. nigricollis.
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J Toxicol,
2010,
837864.
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R.Doley,
S.P.Mackessy,
and
R.M.Kini
(2009).
Role of accelerated segment switch in exons to alter targeting (ASSET) in the molecular evolution of snake venom proteins.
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BMC Evol Biol,
9,
146.
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A.Galat,
G.Gross,
P.Drevet,
A.Sato,
and
A.Ménez
(2008).
Conserved structural determinants in three-fingered protein domains.
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FEBS J,
275,
3207-3225.
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A.V.Osipov,
I.E.Kasheverov,
Y.V.Makarova,
V.G.Starkov,
O.V.Vorontsova,
R.K.h.Ziganshin,
T.V.Andreeva,
M.V.Serebryakova,
A.Benoit,
R.C.Hogg,
D.Bertrand,
V.I.Tsetlin,
and
Y.N.Utkin
(2008).
Naturally occurring disulfide-bound dimers of three-fingered toxins: a paradigm for biological activity diversification.
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J Biol Chem,
283,
14571-14580.
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I.Hudáky,
and
A.Perczel
(2008).
Prolylproline unit in model peptides and in fragments from databases.
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Proteins,
70,
1389-1407.
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R.Mir,
M.Sinha,
S.Sharma,
N.Singh,
P.Kaur,
A.Srinivasan,
and
T.P.Singh
(2008).
Isolation, purification, crystallization and preliminary crystallographic studies of sagitoxin, an oligomeric cardiotoxin from the venom of Naja naja saggitifera.
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Acta Crystallogr Sect F Struct Biol Cryst Commun,
64,
545-547.
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S.C.Lee,
H.H.Guan,
C.H.Wang,
W.N.Huang,
S.C.Tjong,
C.J.Chen,
and
W.G.Wu
(2005).
Structural basis of citrate-dependent and heparan sulfate-mediated cell surface retention of cobra cardiotoxin A3.
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J Biol Chem,
280,
9567-9577.
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PDB code:
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F.Forouhar,
W.N.Huang,
J.H.Liu,
K.Y.Chien,
W.G.Wu,
and
C.D.Hsiao
(2003).
Structural basis of membrane-induced cardiotoxin A3 oligomerization.
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J Biol Chem,
278,
21980-21988.
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PDB code:
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P.Paaventhan,
J.S.Joseph,
S.Nirthanan,
G.Rajaseger,
P.Gopalakrishnakone,
M.R.Kini,
and
P.R.Kolatkar
(2003).
Crystallization and preliminary X-ray analysis of candoxin, a novel reversible neurotoxin from the Malayan krait Bungarus candidus.
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Acta Crystallogr D Biol Crystallogr,
59,
584-586.
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P.V.Dubovskii,
D.M.Lesovoy,
M.A.Dubinnyi,
Y.N.Utkin,
and
A.S.Arseniev
(2003).
Interaction of the P-type cardiotoxin with phospholipid membranes.
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Eur J Biochem,
270,
2038-2046.
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L.Watanabe,
S.Nirthanan,
G.Rajaseger,
I.Polikarpov,
R.M.Kini,
and
R.K.Arni
(2002).
Crystallization and preliminary X-ray analysis of bucain, a novel toxin from the Malayan krait Bungarus candidus.
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Acta Crystallogr D Biol Crystallogr,
58,
1879-1881.
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S.Nirthanan,
E.Charpantier,
P.Gopalakrishnakone,
M.C.Gwee,
H.E.Khoo,
L.S.Cheah,
D.Bertrand,
and
R.M.Kini
(2002).
Candoxin, a novel toxin from Bungarus candidus, is a reversible antagonist of muscle (alphabetagammadelta ) but a poorly reversible antagonist of neuronal alpha 7 nicotinic acetylcholine receptors.
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J Biol Chem,
277,
17811-17820.
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J.F.Gaucher,
R.Ménez,
B.Arnoux,
J.Pusset,
and
A.Ducruix
(2000).
High resolution x-ray analysis of two mutants of a curaremimetic snake toxin.
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Eur J Biochem,
267,
1323-1329.
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PDB codes:
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D.V.Dementieva,
E.V.Bocharov,
and
A.S.Arseniev
(1999).
Two forms of cytotoxin II (cardiotoxin) from Naja naja oxiana in aqueous solution: spatial structures with tightly bound water molecules.
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Eur J Biochem,
263,
152-162.
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PDB codes:
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J.D.Pédelacq,
L.Maveyraud,
G.Prévost,
L.Baba-Moussa,
A.González,
E.Courcelle,
W.Shepard,
H.Monteil,
J.P.Samama,
and
L.Mourey
(1999).
The structure of a Staphylococcus aureus leucocidin component (LukF-PV) reveals the fold of the water-soluble species of a family of transmembrane pore-forming toxins.
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Structure,
7,
277-287.
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PDB code:
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N.Li,
M.Erman,
W.Pangborn,
W.L.Duax,
C.M.Park,
J.Bruenn,
and
D.Ghosh
(1999).
Structure of Ustilago maydis killer toxin KP6 alpha-subunit. A multimeric assembly with a central pore.
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J Biol Chem,
274,
20425-20431.
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PDB code:
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V.Tsetlin
(1999).
Snake venom alpha-neurotoxins and other 'three-finger' proteins.
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Eur J Biochem,
264,
281-286.
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H.V.Patel,
A.A.Vyas,
K.A.Vyas,
Y.S.Liu,
C.M.Chiang,
L.M.Chi,
and
W.Wu
(1997).
Heparin and heparan sulfate bind to snake cardiotoxin. Sulfated oligosaccharides as a potential target for cardiotoxin action.
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J Biol Chem,
272,
1484-1492.
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P.R.Mittl,
S.Di Marco,
G.Fendrich,
G.Pohlig,
J.Heim,
C.Sommerhoff,
H.Fritz,
J.P.Priestle,
and
M.G.Grütter
(1997).
A new structural class of serine protease inhibitors revealed by the structure of the hirustasin-kallikrein complex.
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Structure,
5,
253-264.
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PDB code:
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S.C.Sue,
P.K.Rajan,
T.S.Chen,
C.H.Hsieh,
and
W.Wu
(1997).
Action of Taiwan cobra cardiotoxin on membranes: binding modes of a beta-sheet polypeptide with phosphatidylcholine bilayers.
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Biochemistry,
36,
9826-9836.
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Y.J.Sun,
W.G.Wu,
C.M.Chiang,
A.Y.Hsin,
and
C.D.Hsiao
(1997).
Crystal structure of cardiotoxin V from Taiwan cobra venom: pH-dependent conformational change and a novel membrane-binding motif identified in the three-finger loops of P-type cardiotoxin.
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Biochemistry,
36,
2403-2413.
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PDB code:
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C.M.Chiang,
K.Y.Chien,
H.J.Lin,
J.F.Lin,
H.C.Yeh,
P.L.Ho,
and
W.G.Wu
(1996).
Conformational change and inactivation of membrane phospholipid-related activity of cardiotoxin V from Taiwan cobra venom at acidic pH.
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Biochemistry,
35,
9167-9176.
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C.M.Chiang,
S.L.Chang,
H.J.Lin,
and
W.G.Wu
(1996).
The role of acidic amino acid residues in the structural stability of snake cardiotoxins.
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Biochemistry,
35,
9177-9186.
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M.Dauplais,
J.M.Neumann,
S.Pinkasfeld,
A.Ménez,
and
C.Roumestand
(1995).
An NMR study of the interaction of cardiotoxin gamma from Naja nigricollis with perdeuterated dodecylphosphocholine micelles.
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Eur J Biochem,
230,
213-220.
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M.Jolkkonen,
P.L.Van Giersbergen,
U.Hellman,
C.Wernstedt,
A.Oras,
N.Satyapan,
A.Adem,
and
E.Karlsson
(1995).
Muscarinic toxins from the black mamba Dendroaspis polylepis.
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Eur J Biochem,
234,
579-585.
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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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