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PDBsum entry 3cln
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Calcium binding protein
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PDB id
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3cln
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References listed in PDB file
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Key reference
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Title
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Structure of calmodulin refined at 2.2 a resolution.
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Authors
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Y.S.Babu,
C.E.Bugg,
W.J.Cook.
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Ref.
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J Mol Biol, 1988,
204,
191-204.
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PubMed id
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Abstract
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The crystal structure of mammalian calmodulin has been refined at 2.2 A (1 A =
0.1 nm) resolution using a restrained least-squares method. The final
crystallographic R-factor, based on 6685 reflections in the range 2.2 A less
than or equal to d less than or equal to 5.0 A with intensities exceeding 2.5
sigma, is 0.175. Bond lengths and bond angles in the molecule have
root-mean-square deviations from ideal values of 0.016 A and 1.7 degrees,
respectively. The refined model includes residues 5 to 147, four Ca2+ and 69
water molecules per molecule of calmodulin. The electron density for residues 1
to 4 and 148 is poorly defined, and they are not included in the model. The
molecule is shaped somewhat like a dumbbell, with an overall length of 65 A; the
two lobes are connected by a seven-turn alpha-helix. Prominent secondary
structural features include seven alpha-helices, four Ca2+-binding loops, and
two short, double-stranded antiparallel beta-sheets between pairs of adjacent
Ca2+-binding loops. The four Ca2+-binding domains in calmodulin have a typical
EF hand conformation (helix-loop-helix) and are similar to those described in
other Ca2+-binding proteins. The X-ray structure determination of calmodulin
shows a large hydrophobic cleft in each half of the molecule. These hydrophobic
regions probably represent the sites of interaction with many of the
pharmacological agents known to bind to calmodulin.
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Secondary reference #1
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Title
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Three-Dimensional structure of calmodulin.
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Authors
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Y.S.Babu,
J.S.Sack,
T.J.Greenhough,
C.E.Bugg,
A.R.Means,
W.J.Cook.
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Ref.
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Nature, 1985,
315,
37-40.
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PubMed id
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Secondary reference #2
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Title
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Preparation of calmodulin crystals.
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Authors
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W.J.Cook,
J.S.Sack.
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Ref.
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Methods Enzymol, 1983,
102,
143-147.
[DOI no: ]
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PubMed id
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Secondary reference #3
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Title
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Chicken calmodulin genes. A species comparison of cdna sequences and isolation of a genomic clone.
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Authors
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J.A.Putkey,
K.F.Ts'Ui,
T.Tanaka,
L.Lagacé,
J.P.Stein,
E.C.Lai,
A.R.Means.
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Ref.
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J Biol Chem, 1983,
258,
11864-11870.
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PubMed id
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Secondary reference #4
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Title
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Crystallization and preliminary X-Ray investigation of calmodulin.
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Authors
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W.J.Cook,
J.R.Dedman,
A.R.Means,
C.E.Bugg.
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Ref.
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J Biol Chem, 1980,
255,
8152-8153.
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PubMed id
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