... Solution structure of E. coli DnaG- C
FEBS Journal 273 (2006) 4997–5009 ª 2006 The Authors Journal compilation ª 2006 FEBS 5009
Monomeric solution structure of the helicase-binding
domain of Escherichia ... residues 1–171 of E. coli DnaB helicase; DnaB-N, the N-terminal domain (residues 24–136) of E. coli DnaB helicase; DnaG- C,
the C-terminal doma...
... been
determined in solution. The overall fold and the structure of the b-strand
core of the protein in solution are similar to those found in the crystal
structure. The structure of the minidomain (residues ... faster exchange of
the amide proton of Gly337 with water. The second
A
BC
D
E
Fig. 3. The solution structure of the
C -domain. (A) Stereo...
... establish the preferred geometry of the
precursor. We now report the chemical synthesis, bio-
chemical production, and solution structure of preCbnB2,
and compare it with the structure of the mature
bacteriocin, ... Solution structure of preCbnB2 in 70% trifluoroethanol. The
positions of the N-terminus and C-terminus are indicated, as are
the residues at th...
... capable of discriminating between
Na
+
-channel isoforms of the same organism (e.g. the rat
brain isoform rNa
V
1.1 is 10-fold more sensitive to the action
of the a Na-ScTx Lqq5 than the cardiac isoform ... (E
Na
¼
)65). To determine the amplitude of the toxin-induced slow
inactivation, we subtracted the control traces from the traces
recorded in the presence of...
... Nerbonne (2006). In both of
these papers the identification of linguistic structure
in the aggregate analysis is based on the analysis of
the pronunciation of the vowels found in the data set.
In work ... the underlying linguistic structure, i.e.
the specific linguistic elements that contributed to
the differences between the dialects. This is very of-
ten seen...
... other proteins. The active site of enolase is present
at the C terminus of this barrel. The small or N-terminal
domain wraps around the outside of the main domain [8].
Most of the intersubunit ... between the small
domain of one monomer and the large domain of the other.
Kinetic experiments have demonstrated that binding of two
metal ions to each monome...
... A comparison of the structure of the unli-
ganded cathepsin B with the structure of the proenzyme, its complexes with
chagasin and stefin A shows that the magnitude of the shift of the occlud-
ing ... [20].
Although the structures of the mature native form
of cathepsin B clearly exposed the relevance of the
occluding loop for the exopeptidase activit...
... N-glycans
located on either the b-propeller of a
5
[55] or the I-like
domain of b
1
or b
3
[68] contribute to the regulation of
integrin function. Therefore, we speculate that modifi-
cation of particular ... Down-
regulation of the alpha-Gal epitope expression in N-gly-
cans of swine endothelial cells by transfection with the
N-acetylglucosaminyltransferase III gene. M...
... change the
preference of site utilization; and (c) promotion of the
dissociation of Chordin cysteine-rich (CR)-containing
fragments from the ligand. They suggest that the first
of these three is the ... transmembrane domain. Bind-
ing of the ligand to the receptor complex induces
the type II receptor to phosphorylate the type I
receptor, which then leads to activat...
... torque of 112 pNÆnm, the
arrows show the beginning (t ¼ 1ns)andtheend(t¼
23 ns) of the forced rotation. With 56 pNÆnm torque, the
relaxation of the system was calculated during the last 8 ns
of the ... during the f orced
molecular dynamics calculated with the torque of 56 pNÆnm. The
secondary structure of c is shown for the time of 1 ns (the end of ini...