... other Ab fragments, including full-
length Ab.
The two most abundant forms of < /b> Ab are the 40
and 42 residue peptides, Ab
1)40
and Ab
1)42
. Both
forms are capable of < /b> assembling into b- sheet fibrils.
However, ... [13–15].
The study of < /b> hydrogen–deuterium exchange mapping
of < /b> Ab using NMR revealed that the middle of < /b> Ab is
involved in a b structure < /b>...
... then it can be stated that the root
of < /b> every tree of < /b> the mentioned kind is
labelled by a symbol the lexical part of < /b>
which belongs to the word class of < /b> verbs.
The kinds (and to a certain part ... to be used for an-
other set of < /b> tasks, including the anal-
ysis of < /b> a broader set of < /b> input texts,
questions, etc.);
(b) linguistic meaning is ~...
... Increase
epi-Inositol b- Sheet No effect Inhibits Inhibits Inhibits
L-epi-1-Inosose Partial b- sheet No effect No effect No effect Increase
L-epi-2-Inosose Strong b- sheet < Control Inhibits Inhibits Inhibits
allo-Inositol ... that allo-inositol is a kinetic inhibitor of < /b> Ab42
fiber formation but is unable to fully inhibit fiber for-
mation. These results further suggest that allo-i...
... Grubb A (2004) Prevention
of < /b> domain swapping inhibits dimerization and amyloid
< /b> fibril formation of < /b> cystatin C: use of < /b> engineered disul-
fide bridges, antibodies, and carboxymethylpapain to
stabilize ... that the b- sheet spine in
amyloid < /b> fibrils of < /b> b
2
-microglobulin could be made
from amyloidogenic peptide sequences of < /b> the hinge
regions o...
... Tyr42 (in RNase T1) or an arginine (in
RNase Sa, barnase, and binase) has an important role
in closing the guanine-binding site [10,15–17]. How-
ever, although the interactions between guanine and
the ... molecules, guanosine formed the high-
est number of < /b> hydrogen bonds of < /b> all the bases, up to
five, and had the best fit into the base-binding site. In
addition, guanine under...
... by a two-step mechanism in which
the N-terminus of < /b> the inhibitor first binds to the
enzyme, displacing the occluding loop, followed by the
binding of < /b> another two loops of < /b> the inhibitor [24].
Besides ... FEBS
Friguet et al. [30] and was found to be 2.7 ± 1.8 nm,
depicting a strong interaction between 2A2 mAb and
cathepsin B.
Determination of < /b> the 2A2 mAb binding s...
... properties, thereby providing a broad binding speci-
ficity. In some proteins containing tandem homologous
domains, inter-domain interactions fix the relative ori-
entation of < /b> the domains in a specific ... and boxes (blue for the
N-terminal domain; red for the C-terminal
domain) indicate some of < /b> the perturbed
resonances.
M. Takeda et al. SAIL-NMR structure < /b> of < /b> a my...
... amount of < /b> substrate remaining was quantitated by
HPLC as described in the text and in the legend to Table 1.
286 G. V. B. Reddy et al. (Eur. J. Biochem. 270) Ó FEBS 2003
conducted in the absence of < /b> ... was oxidized. In addition, while about 30%
of < /b> the diarylpropane VI was oxidized in the presence of
< /b> Tween 80 during the 12 h incubation, in the absence...
... roteins as well as amastatin bound to LAP a s d iscu ssed in the text .
Ó FEBS 2002 Structure < /b> of < /b> peptidase T (Eur. J. Biochem. 269) 447
Substrate binding
Structural investigation of < /b> enzyme±ligand complexes ... substrate bindin g site has been m apped
based on our knowledge of < /b> the structures of < /b> leucine
aminopeptidase (LAP) and APP [18,19]. It has been point...
... homodimer of < /b> a single-transmembrane
polypeptide, each containing an extracellular ANP-
binding domain (ECD), a transmembrane domain, and
an intracellular domain consisting of < /b> an ATP-binding
regulatory ... juxta-
membrane domains in response to ANP binding. Looking down-
wards toward the cell membrane, ANP binding causes a translation
of < /b> the juxtamembrane domains from t...