 |
PDBsum entry 1txb
|
|
|
|
 |
Contents |
 |
|
|
|
|
|
|
|
* Residue conservation analysis
|
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
| |
|
DOI no:
|
J Biol Chem
272:7817-7823
(1997)
|
|
PubMed id:
|
|
|
|
|
| |
|
Solution structure of toxin b, a long neurotoxin from the venom of the king cobra (Ophiophagus hannah).
|
|
S.S.Peng,
T.K.Kumar,
G.Jayaraman,
C.C.Chang,
C.Yu.
|
|
|
|
| |
ABSTRACT
|
|
|
| |
|
The solution structure of toxin b, a long neurotoxin (73 amino acids and 5
disulfides) from the venom of Ophiophagus hannah (king cobra), has been
determined using 1H NMR and dynamical simulated annealing techniques. The
structures were calculated using 485 distance constraints and 52 dihedral angle
restraints. The 21 structures that were obtained satisfy the experimental
restraints and possess good nonbonded contacts. Analysis of the converged
structures revealed that the protein consists of a core region from which three
finger-like loops extend outwards. The regular secondary structure in toxin b
includes a double and a triple stranded antiparallel beta sheet. Comparison with
the solution structures of other long neurotoxins reveals that although the
structure of toxin b is similar to those of previously reported long
neurotoxins, clear local structural differences are observed in regions proposed
to be involved in binding to the acetylcholine receptor. A positively charged
cluster is found in the C-terminal tail, in Loop III, and in the tip of Loop II.
This cationic cluster could be crucial for the binding of the long neurotoxins
to the acetylcholine receptor.
|
|
|
|
|
| |
Selected figure(s)
|
|
|
| |
 |
 |
|
 |
|
 |
Figure 4.
Fig. 4. Sequence distribution of the NOE constraints used in
the calculation of solution structures of Oh-8. The various NOE^
constraints used in the structure calculation include
intra-residual (hatched), sequential (white), medium range
(dotted), and long range (black).
|
 |
Figure 9.
Fig. 9. GRASP representation of the distribution of the
positively (blue) and negatively (red) charged residues of toxin
b. The positively charged cluster constituted from cationic
residues in the C-terminal tail, Loop III, and Loop II is
involved in the^ binding of the toxin to the acetylcholine
receptor.
|
 |
|
|
|
| |
The above figures are
reprinted
by permission from the ASBMB:
J Biol Chem
(1997,
272,
7817-7823)
copyright 1997.
|
|
| |
Figures were
selected
by an automated process.
|
|
|
|
|
 |
 |
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
Literature references that cite this PDB file's key reference
|
|
 |
| |
PubMed id
|
 |
Reference
|
 |
|
|
|
 |
L.Bracci,
A.Pini,
L.Lozzi,
B.Lelli,
P.Battestin,
A.Spreafico,
A.Bernini,
N.Niccolai,
and
P.Neri
(2001).
Mimicking the nicotinic receptor binding site by a single chain Fv selected by competitive panning from a synthetic phage library.
|
| |
J Neurochem,
78,
24-31.
|
 |
|
|
|
|
 |
E.J.Ackermann,
and
P.Taylor
(1997).
Nonidentity of the alpha-neurotoxin binding sites on the nicotinic acetylcholine receptor revealed by modification in alpha-neurotoxin and receptor structures.
|
| |
Biochemistry,
36,
12836-12844.
|
 |
|
 |
 |
|
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.
|
');
}
}
 |