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PDBsum entry 1cdp
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Calcium binding
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PDB id
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1cdp
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Contents |
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* Residue conservation analysis
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J Biol Chem
264:16620-16628
(1989)
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PubMed id:
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Restrained least squares refinement of native (calcium) and cadmium-substituted carp parvalbumin using X-ray crystallographic data at 1.6-A resolution.
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A.L.Swain,
R.H.Kretsinger,
E.L.Amma.
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ABSTRACT
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Carp parvalbumin coordinates calcium through one carbonyl oxygen atom and the
oxygen-containing side chains of 5 amino acid residues, or 4 residues and a
water molecule, in a helix-loop-helix structural motif. Other calcium-binding
proteins, including calmodulin and troponin C, also possess this unique
calcium-binding design, which is designated EF-hand or calmodulin fold.
Parvalbumin has two such sites, labeled CD and EF. Each of the calcium-binding
sites of refined structures of proteins belonging to this group has a 7-oxygen
coordination sphere except those of the structure of parvalbumin as it was
reported in 1975. This structure had been refined at 1.9 A using difference
Fourier techniques on film data. The CD site appeared to be 6-coordinate and the
EF site 8-coordinate. Results of NMR experiments using 113Cd-substituted
parvalbumin, however, indicate that the sites are similar to one another with
coordination number greater than 6. To resolve the inconsistency between
crystallographic and NMR results, 1.6 A area detector data was collected for
native and cadmium-substituted parvalbumin; the structures have been refined to
R factors of 18.7% and 16.4%, respectively, with acceptable geometry and low
errors in atomic coordinates. Differences between the parvalbumin structure
described in 1975 and the present structure are addressed, including the
discovery of 7-coordination for both the CD and EF sites.
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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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E.Papaleo,
and
G.Invernizzi
(2011).
Conformational plasticity of the calcium-binding pocket in the Burkholderia glumae lipase: Remodeling induced by mutation of calcium coordinating residues.
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Biopolymers,
95,
117-126.
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M.T.Henzl,
J.J.Tanner,
and
A.Tan
(2011).
Solution structures of chicken parvalbumin 3 in the Ca(2+) -free and Ca(2+) -bound states.
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Proteins,
79,
752-764.
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PDB codes:
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J.P.Schuermann,
A.Tan,
J.J.Tanner,
and
M.T.Henzl
(2010).
Structure of avian thymic hormone, a high-affinity avian beta-parvalbumin, in the Ca2+-free and Ca2+-bound states.
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J Mol Biol,
397,
991.
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PDB codes:
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M.Kirberger,
and
J.J.Yang
(2008).
Structural differences between Pb2+- and Ca2+-binding sites in proteins: implications with respect to toxicity.
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J Inorg Biochem,
102,
1901-1909.
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N.Juranić,
J.J.Dannenberg,
G.Cornilescu,
P.Salvador,
E.Atanasova,
H.C.Ahn,
S.Macura,
J.L.Markley,
and
F.G.Prendergast
(2008).
Structural dependencies of protein backbone 2JNC' couplings.
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Protein Sci,
17,
768-776.
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C.Charron,
B.Vitoux,
and
A.Aubry
(2002).
Comparative analysis of thermoadaptation within the archaeal glyceraldehyde-3-phosphate dehydrogenases from mesophilic Methanobacterium bryantii and thermophilic Methanothermus fervidus.
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Biopolymers,
65,
263-273.
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K.Truong,
and
M.Ikura
(2002).
Identification and characterization of subfamily-specific signatures in a large protein superfamily by a hidden Markov model approach.
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BMC Bioinformatics,
3,
1.
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M.S.Cates,
M.L.Teodoro,
and
G.N.Phillips
(2002).
Molecular mechanisms of calcium and magnesium binding to parvalbumin.
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Biophys J,
82,
1133-1146.
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S.L.Kazmirski,
R.L.Isaacson,
C.An,
A.Buckle,
C.M.Johnson,
V.Daggett,
and
A.R.Fersht
(2002).
Loss of a metal-binding site in gelsolin leads to familial amyloidosis-Finnish type.
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Nat Struct Biol,
9,
112-116.
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PDB code:
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W.Yang,
H.W.Lee,
H.Hellinga,
and
J.J.Yang
(2002).
Structural analysis, identification, and design of calcium-binding sites in proteins.
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Proteins,
47,
344-356.
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J.Jia,
N.Borregaard,
K.Lollike,
and
M.Cygler
(2001).
Structure of Ca(2+)-loaded human grancalcin.
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Acta Crystallogr D Biol Crystallogr,
57,
1843-1849.
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PDB codes:
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R.C.Richardson,
N.M.King,
D.J.Harrington,
H.Sun,
W.E.Royer,
and
D.J.Nelson
(2000).
X-Ray crystal structure and molecular dynamics simulations of silver hake parvalbumin (Isoform B).
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Protein Sci,
9,
73-82.
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PDB code:
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E.J.van Asselt,
A.J.Dijkstra,
K.H.Kalk,
B.Takacs,
W.Keck,
and
B.W.Dijkstra
(1999).
Crystal structure of Escherichia coli lytic transglycosylase Slt35 reveals a lysozyme-like catalytic domain with an EF-hand.
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Structure,
7,
1167-1180.
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PDB codes:
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J.P.Declercq,
C.Evrard,
V.Lamzin,
and
J.Parello
(1999).
Crystal structure of the EF-hand parvalbumin at atomic resolution (0.91 A) and at low temperature (100 K). Evidence for conformational multistates within the hydrophobic core.
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Protein Sci,
8,
2194-2204.
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PDB code:
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M.S.Cates,
M.B.Berry,
E.L.Ho,
Q.Li,
J.D.Potter,
and
G.N.Phillips
(1999).
Metal-ion affinity and specificity in EF-hand proteins: coordination geometry and domain plasticity in parvalbumin.
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Structure,
7,
1269-1278.
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PDB codes:
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H.Matsumura,
T.Shiba,
T.Inoue,
S.Harada,
and
Y.Kai
(1998).
A novel mode of target recognition suggested by the 2.0 A structure of holo S100B from bovine brain.
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Structure,
6,
233-241.
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PDB code:
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R.R.Biekofsky,
S.R.Martin,
J.P.Browne,
P.M.Bayley,
and
J.Feeney
(1998).
Ca2+ coordination to backbone carbonyl oxygen atoms in calmodulin and other EF-hand proteins: 15N chemical shifts as probes for monitoring individual-site Ca2+ coordination.
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Biochemistry,
37,
7617-7629.
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A.R.Khan,
K.A.Johnson,
J.Braam,
and
M.N.James
(1997).
Comparative modeling of the three-dimensional structure of the calmodulin-related TCH2 protein from Arabidopsis.
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Proteins,
27,
144-153.
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PDB code:
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G.S.Shaw,
and
B.D.Sykes
(1996).
NMR solution structure of a synthetic troponin C heterodimeric domain.
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Biochemistry,
35,
7429-7438.
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PDB code:
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L.Zhang,
and
J.Hermans
(1996).
Hydrophilicity of cavities in proteins.
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Proteins,
24,
433-438.
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C.Donaldson,
K.R.Barber,
C.M.Kay,
and
G.S.Shaw
(1995).
Human S100b protein: formation of a tetramer from synthetic calcium-binding site peptides.
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Protein Sci,
4,
765-772.
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N.N.Khechinashvili,
J.Janin,
and
F.Rodier
(1995).
Thermodynamics of the temperature-induced unfolding of globular proteins.
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Protein Sci,
4,
1315-1324.
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S.M.Gagné,
S.Tsuda,
M.X.Li,
L.B.Smillie,
and
B.D.Sykes
(1995).
Structures of the troponin C regulatory domains in the apo and calcium-saturated states.
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Nat Struct Biol,
2,
784-789.
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PDB codes:
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G.S.Shaw,
R.S.Hodges,
C.M.Kay,
and
B.D.Sykes
(1994).
Relative stabilities of synthetic peptide homo- and heterodimeric troponin-C domains.
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Protein Sci,
3,
1010-1019.
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J.J.Falke,
S.K.Drake,
A.L.Hazard,
and
O.B.Peersen
(1994).
Molecular tuning of ion binding to calcium signaling proteins.
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Q Rev Biophys,
27,
219-290.
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M.H.Zehfus
(1993).
Improved calculations of compactness and a reevaluation of continuous compact units.
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Proteins,
16,
293-300.
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S.T.Rao,
S.Wu,
K.A.Satyshur,
K.Y.Ling,
C.Kung,
and
M.Sundaralingam
(1993).
Structure of Paramecium tetraurelia calmodulin at 1.8 A resolution.
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Protein Sci,
2,
436-447.
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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
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Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
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