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* Residue conservation analysis
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Enzyme class:
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E.C.3.2.1.17
- Lysozyme.
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Reaction:
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Hydrolysis of the 1,4-beta-linkages between N-acetyl-D-glucosamine and N-acetylmuramic acid in peptidoglycan heteropolymers of the prokaryotes cell walls.
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Gene Ontology (GO) functional annotation
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Cellular component
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extracellular region
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2 terms
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Biological process
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metabolic process
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4 terms
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Biochemical function
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catalytic activity
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5 terms
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DOI no:
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Acta Crystallogr D Biol Crystallogr
54:899-904
(1998)
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PubMed id:
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Locations of bromide ions in tetragonal lysozyme crystals.
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K.Lim,
A.Nadarajah,
E.L.Forsythe,
M.L.Pusey.
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ABSTRACT
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Anions have been shown to play a dominant role in the crystallization of chicken
egg-white lysozyme from salt solutions. Previous studies employing X-ray
crystallography have found one chloride ion binding site in the tetragonal
crystal form of the protein and four nitrate ion binding sites in the monoclinic
form. In this study the anion positions in the tetragonal form were determined
from the difference Fourier map obtained from lysozyme crystals grown in bromide
and chloride solutions. Five possible anion-binding sites were found in this
manner. Some of these sites were in pockets containing basic residues while
others were near neutral, but polar, residues. The sole chloride ion binding
site found in previous studies was confirmed, while four further sites were
found which corresponded to the four binding sites found for nitrate ions in
monoclinic crystals. The study suggests that most of the anion-binding sites in
lysozyme remain unchanged even when different anions and different crystal forms
of lysozyme are employed.
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Selected figure(s)
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Figure 3.
Fig. 3. Stereo image of the Hal5 site. Given its relatively small peak in the electron-density difference map (~5a), the location of a bromide ion
here is not certain and is assigned to a water molecule in the refined structure. However, other evidence suggests that this is indeed a valid
anion-binding sitc for lysozyme (see text).
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The above figure is
reprinted
by permission from the IUCr:
Acta Crystallogr D Biol Crystallogr
(1998,
54,
899-904)
copyright 1998.
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Figure was
selected
by an automated process.
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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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Y.R.Gokarn,
R.M.Fesinmeyer,
A.Saluja,
V.Razinkov,
S.F.Chase,
T.M.Laue,
and
D.N.Brems
(2011).
Effective charge measurements reveal selective and preferential accumulation of anions, but not cations, at the protein surface in dilute salt solutions.
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Protein Sci, 20,
580-587.
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B.R.Donald,
and
J.Martin
(2009).
Automated NMR Assignment and Protein Structure Determination using Sparse Dipolar Coupling Constraints.
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Prog Nucl Magn Reson Spectrosc, 55,
101-127.
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T.Yamamoto,
T.Matsuda,
T.Inoue,
H.Matsumura,
M.Morikawa,
S.Kanaya,
and
Y.Kai
(2006).
Crystal structure of TBP-interacting protein (Tk-TIP26) and implications for its inhibition mechanism of the interaction between TBP and TATA-DNA.
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Protein Sci, 15,
152-161.
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PDB code:
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C.J.Langmead,
A.Yan,
R.Lilien,
L.Wang,
and
B.R.Donald
(2004).
A polynomial-time nuclear vector replacement algorithm for automated NMR resonance assignments.
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J Comput Biol, 11,
277-298.
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V.A.Higman,
J.Boyd,
L.J.Smith,
and
C.Redfield
(2004).
Asparagine and glutamine side-chain conformation in solution and crystal: a comparison for hen egg-white lysozyme using residual dipolar couplings.
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J Biomol NMR, 30,
327-346.
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S.Majeed,
G.Ofek,
A.Belachew,
C.C.Huang,
T.Zhou,
and
P.D.Kwong
(2003).
Enhancing protein crystallization through precipitant synergy.
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Structure, 11,
1061-1070.
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PDB code:
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Z.Dauter,
and
M.Dauter
(2001).
Entering a new phase: using solvent halide ions in protein structure determination.
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Structure, 9,
R21-R26.
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T.I.Zarembinski,
L.W.Hung,
H.J.Mueller-Dieckmann,
K.K.Kim,
H.Yokota,
R.Kim,
and
S.H.Kim
(1998).
Structure-based assignment of the biochemical function of a hypothetical protein: a test case of structural genomics.
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Proc Natl Acad Sci U S A, 95,
15189-15193.
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PDB code:
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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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