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PDBsum entry 1ikc
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* Residue conservation analysis
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DOI no:
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Biochemistry
41:1457-1463
(2002)
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PubMed id:
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NMR structure of alpha-bungarotoxin free and bound to a mimotope of the nicotinic acetylcholine receptor.
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M.Scarselli,
O.Spiga,
A.Ciutti,
A.Bernini,
L.Bracci,
B.Lelli,
L.Lozzi,
D.Calamandrei,
D.Di Maro,
S.Klein,
N.Niccolai.
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ABSTRACT
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A combinatorial library approach was used to produce synthetic peptides
mimicking the snake neurotoxin binding site of nicotinic receptors. Among the
sequences, which inhibited binding of alpha-bungarotoxin to muscle and neuronal
nicotinic receptors, HRYYESSLPWYPD, a 14-amino acid peptide with considerably
higher toxin-binding affinity than the other synthesized peptides, was selected,
and the structure of its complex with the toxin was analyzed by NMR. Comparison
of the solution structure of the free toxin and its complex with this peptide
indicated that complex formation induced extensive conformational rearrangements
mainly at finger II and the carboxy terminus of the protein. The peptidyl
residues P10 and Y4 seemed to be critical for peptide folding and complex
stability, respectively. The latter residue of the peptide strongly interacted
with the protein by entering a small pocket delimited by D30, C33, S34, R36, and
V39 toxin side chains.
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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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A.O.Samson,
J.H.Chill,
and
J.Anglister
(2005).
Two-dimensional measurement of proton T1rho relaxation in unlabeled proteins: mobility changes in alpha-bungarotoxin upon binding of an acetylcholine receptor peptide.
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Biochemistry,
44,
10926-10934.
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M.Talebzadeh-Farooji,
M.Amininasab,
M.M.Elmi,
H.Naderi-Manesh,
and
M.N.Sarbolouki
(2004).
Solution structure of long neurotoxin NTX-1 from the venom of Naja naja oxiana by 2D-NMR spectroscopy.
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Eur J Biochem,
271,
4950-4957.
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PDB code:
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H.S.Young,
L.G.Herbette,
and
V.Skita
(2003).
Alpha-bungarotoxin binding to acetylcholine receptor membranes studied by low angle X-ray diffraction.
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Biophys J,
85,
943-953.
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L.Lozzi,
B.Lelli,
Y.Runci,
S.Scali,
A.Bernini,
C.Falciani,
A.Pini,
N.Niccolai,
P.Neri,
and
L.Bracci
(2003).
Rational design and molecular diversity for the construction of anti-alpha-bungarotoxin antidotes with high affinity and in vivo efficiency.
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Chem Biol,
10,
411-417.
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S.W.Chi,
K.H.Park,
J.E.Suk,
B.M.Olivera,
J.M.McIntosh,
and
K.H.Han
(2003).
Solution conformation of alphaA-conotoxin EIVA, a potent neuromuscular nicotinic acetylcholine receptor antagonist from Conus ermineus.
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J Biol Chem,
278,
42208-42213.
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PDB code:
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A.Samson,
T.Scherf,
M.Eisenstein,
J.Chill,
and
J.Anglister
(2002).
The mechanism for acetylcholine receptor inhibition by alpha-neurotoxins and species-specific resistance to alpha-bungarotoxin revealed by NMR.
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Neuron,
35,
319-332.
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PDB codes:
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F.Teixeira-Clerc,
A.Ménez,
and
P.Kessler
(2002).
How do short neurotoxins bind to a muscular-type nicotinic acetylcholine receptor?
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J Biol Chem,
277,
25741-25747.
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L.Bracci,
L.Lozzi,
A.Pini,
B.Lelli,
C.Falciani,
N.Niccolai,
A.Bernini,
A.Spreafico,
P.Soldani,
and
P.Neri
(2002).
A branched peptide mimotope of the nicotinic receptor binding site is a potent synthetic antidote against the snake neurotoxin alpha-bungarotoxin.
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Biochemistry,
41,
10194-10199.
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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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