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PDBsum entry 1of4
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Hydrolase/carbohydrate binding
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PDB id
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1of4
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Contents |
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* Residue conservation analysis
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DOI no:
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Structure
11:665-675
(2003)
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PubMed id:
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Structural and thermodynamic dissection of specific mannan recognition by a carbohydrate binding module, TmCBM27.
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A.B.Boraston,
T.J.Revett,
C.M.Boraston,
D.Nurizzo,
G.J.Davies.
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ABSTRACT
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The C-terminal 176 amino acids of a Thermotoga maritima mannanase (Man5)
constitute a carbohydrate binding module (CBM) that has been classified into CBM
family 27. The isolated CBM27 domain, named TmCBM27, binds tightly (K(a)s
10(5)-10(6) M(-1)) to beta-1, 4-mannooligosaccharides, carob galactomannan, and
konjac glucomannan, but not to cellulose (insoluble and soluble) or soluble
birchwood xylan. The X-ray crystal structures of native TmCBM27, a
TmCBM27-mannohexaose complex, and a
TmCBM27-6(3),6(4)-alpha-D-galactosyl-mannopentaose complex at 2.0 A, 1.6 A, and
1.35 A, respectively, reveal the basis of TmCBM27's specificity for mannans. In
particular, the latter complex, which is the first structure of a CBM in complex
with a branched plant cell wall polysaccharide, illustrates how the architecture
of the binding site can influence the recognition of naturally substituted
polysaccharides.
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Selected figure(s)
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Figure 7.
Figure 7. A Schematic Showing the Interactions of TmCBM27
with G[2]M[5] (A) and Mannohexaose (B)Hydrogen bonds, dashed
lines; water molecules, filled circles. Binding subsites
referred to in the text are shown underneath the schematics with
brackets.
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The above figure is
reprinted
by permission from Cell Press:
Structure
(2003,
11,
665-675)
copyright 2003.
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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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N.S.Pannu,
W.J.Waterreus,
P.Skubák,
I.Sikharulidze,
J.P.Abrahams,
and
R.A.de Graaff
(2011).
Recent advances in the CRANK software suite for experimental phasing.
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Acta Crystallogr D Biol Crystallogr,
67,
331-337.
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P.Skubák,
W.J.Waterreus,
and
N.S.Pannu
(2010).
Multivariate phase combination improves automated crystallographic model building.
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Acta Crystallogr D Biol Crystallogr,
66,
783-788.
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S.E.Marcus,
A.W.Blake,
T.A.Benians,
K.J.Lee,
C.Poyser,
L.Donaldson,
O.Leroux,
A.Rogowski,
H.L.Petersen,
A.Boraston,
H.J.Gilbert,
W.G.Willats,
and
J.P.Knox
(2010).
Restricted access of proteins to mannan polysaccharides in intact plant cell walls.
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Plant J,
64,
191-203.
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M.Tanaka,
Y.Umemoto,
H.Okamura,
D.Nakano,
Y.Tamaru,
and
T.Araki
(2009).
Cloning and characterization of a beta-1,4-mannanase 5C possessing a family 27 carbohydrate-binding module from a marine bacterium, Vibrio sp. strain MA-138.
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Biosci Biotechnol Biochem,
73,
109-116.
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N.Forsgren,
R.J.Lamont,
and
K.Persson
(2009).
Crystal structure of the variable domain of the Streptococcus gordonii surface protein SspB.
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Protein Sci,
18,
1896-1905.
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PDB code:
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J.Henshaw,
A.Horne-Bitschy,
A.L.van Bueren,
V.A.Money,
D.N.Bolam,
M.Czjzek,
N.A.Ekborg,
R.M.Weiner,
S.W.Hutcheson,
G.J.Davies,
A.B.Boraston,
and
H.J.Gilbert
(2006).
Family 6 carbohydrate binding modules in beta-agarases display exquisite selectivity for the non-reducing termini of agarose chains.
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J Biol Chem,
281,
17099-17107.
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PDB codes:
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S.Najmudin,
C.I.Guerreiro,
A.L.Carvalho,
J.A.Prates,
M.A.Correia,
V.D.Alves,
L.M.Ferreira,
M.J.Romão,
H.J.Gilbert,
D.N.Bolam,
and
C.M.Fontes
(2006).
Xyloglucan is recognized by carbohydrate-binding modules that interact with beta-glucan chains.
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J Biol Chem,
281,
8815-8828.
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PDB codes:
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J.Flint,
D.N.Bolam,
D.Nurizzo,
E.J.Taylor,
M.P.Williamson,
C.Walters,
G.J.Davies,
and
H.J.Gilbert
(2005).
Probing the mechanism of ligand recognition in family 29 carbohydrate-binding modules.
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J Biol Chem,
280,
23718-23726.
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PDB codes:
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P.Skubák,
S.Ness,
and
N.S.Pannu
(2005).
Extending the resolution and phase-quality limits in automated model building with iterative refinement.
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Acta Crystallogr D Biol Crystallogr,
61,
1626-1635.
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S.B.Conners,
C.I.Montero,
D.A.Comfort,
K.R.Shockley,
M.R.Johnson,
S.R.Chhabra,
and
R.M.Kelly
(2005).
An expression-driven approach to the prediction of carbohydrate transport and utilization regulons in the hyperthermophilic bacterium Thermotoga maritima.
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J Bacteriol,
187,
7267-7282.
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Y.Hatada,
N.Takeda,
K.Hirasawa,
Y.Ohta,
R.Usami,
Y.Yoshida,
W.D.Grant,
S.Ito,
and
K.Horikoshi
(2005).
Sequence of the gene for a high-alkaline mannanase from an alkaliphilic Bacillus sp. strain JAMB-750, its expression in Bacillus subtilis and characterization of the recombinant enzyme.
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Extremophiles,
9,
497-500.
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A.L.Carvalho,
A.Goyal,
J.A.Prates,
D.N.Bolam,
H.J.Gilbert,
V.M.Pires,
L.M.Ferreira,
A.Planas,
M.J.Romão,
and
C.M.Fontes
(2004).
The family 11 carbohydrate-binding module of Clostridium thermocellum Lic26A-Cel5E accommodates beta-1,4- and beta-1,3-1,4-mixed linked glucans at a single binding site.
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J Biol Chem,
279,
34785-34793.
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PDB code:
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D.N.Bolam,
H.Xie,
G.Pell,
D.Hogg,
G.Galbraith,
B.Henrissat,
and
H.J.Gilbert
(2004).
X4 modules represent a new family of carbohydrate-binding modules that display novel properties.
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J Biol Chem,
279,
22953-22963.
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F.M.Dias,
F.Vincent,
G.Pell,
J.A.Prates,
M.S.Centeno,
L.E.Tailford,
L.M.Ferreira,
C.M.Fontes,
G.J.Davies,
and
H.J.Gilbert
(2004).
Insights into the molecular determinants of substrate specificity in glycoside hydrolase family 5 revealed by the crystal structure and kinetics of Cellvibrio mixtus mannosidase 5A.
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J Biol Chem,
279,
25517-25526.
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PDB code:
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J.L.Henshaw,
D.N.Bolam,
V.M.Pires,
M.Czjzek,
B.Henrissat,
L.M.Ferreira,
C.M.Fontes,
and
H.J.Gilbert
(2004).
The family 6 carbohydrate binding module CmCBM6-2 contains two ligand-binding sites with distinct specificities.
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J Biol Chem,
279,
21552-21559.
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Z.Fujimoto,
S.Kaneko,
A.Kuno,
H.Kobayashi,
I.Kusakabe,
and
H.Mizuno
(2004).
Crystal structures of decorated xylooligosaccharides bound to a family 10 xylanase from Streptomyces olivaceoviridis E-86.
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J Biol Chem,
279,
9606-9614.
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PDB codes:
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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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