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PDBsum entry 1smg
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Calcium-binding protein
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PDB id
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1smg
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Contents |
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* Residue conservation analysis
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DOI no:
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Biochemistry
36:4386-4392
(1997)
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PubMed id:
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Mechanism of direct coupling between binding and induced structural change in regulatory calcium binding proteins.
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S.M.Gagné,
M.X.Li,
B.D.Sykes.
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ABSTRACT
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The structural transition in troponin C induced by the binding of two calcium
ions involves an "opening" of the structure, an event that triggers skeletal
muscle contraction. We have solved the solution structure of a mutant (E41A) of
the regulatory domain of skeletal troponin C wherein one bidentate ligand to the
calcium in site I is missing. This structure remains "closed" upon calcium
binding, indicating that the linkage between calcium binding and the induced
conformational change has been broken. This provides a snapshot of skeletal
troponin C between the off and on state and thereby valuable insight into the
mechanism of regulation within skeletal TnC. Although several factors contribute
to the triggering mechanism, the opening of the troponin C structure is
ultimately dependent on one amino acid, Glu41. Insights into the structure of
cardiac troponin C can also be derived from this skeletal mutant.
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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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L.Santamaria-Kisiel,
and
G.S.Shaw
(2011).
Identification of regions responsible for the open conformation of S100A10 using chimaeric S100A11-S100A10 proteins.
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Biochem J,
434,
37-48.
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Z.Grabarek
(2011).
Insights into modulation of calcium signaling by magnesium in calmodulin, troponin C and related EF-hand proteins.
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Biochim Biophys Acta,
1813,
913-921.
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L.W.Xiong,
Q.K.Kleerekoper,
X.Wang,
and
J.A.Putkey
(2010).
Intra- and interdomain effects due to mutation of calcium-binding sites in calmodulin.
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J Biol Chem,
285,
8094-8103.
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R.M.Hoffman,
and
B.D.Sykes
(2009).
Structure of the inhibitor W7 bound to the regulatory domain of cardiac troponin C.
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Biochemistry,
48,
5541-5552.
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PDB code:
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S.L.Shirran,
and
P.E.Barran
(2009).
The use of ESI-MS to probe the binding of divalent cations to calmodulin.
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J Am Soc Mass Spectrom,
20,
1159-1171.
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C.N.Chi,
L.Elfström,
Y.Shi,
T.Snäll,
A.Engström,
and
P.Jemth
(2008).
Reassessing a sparse energetic network within a single protein domain.
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Proc Natl Acad Sci U S A,
105,
4679-4684.
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M.C.Suarez,
C.B.Rocha,
M.M.Sorenson,
J.L.Silva,
and
D.Foguel
(2008).
Free-energy linkage between folding and calcium binding in EF-hand proteins.
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Biophys J,
95,
4820-4828.
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F.Capozzi,
F.Casadei,
and
C.Luchinat
(2006).
EF-hand protein dynamics and evolution of calcium signal transduction: an NMR view.
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J Biol Inorg Chem,
11,
949-962.
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T.M.Blumenschein,
D.B.Stone,
R.J.Fletterick,
R.A.Mendelson,
and
B.D.Sykes
(2005).
Calcium-dependent changes in the flexibility of the regulatory domain of troponin C in the troponin complex.
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J Biol Chem,
280,
21924-21932.
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I.Marcotte,
F.Separovic,
M.Auger,
and
S.M.Gagné
(2004).
A multidimensional 1H NMR investigation of the conformation of methionine-enkephalin in fast-tumbling bicelles.
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Biophys J,
86,
1587-1600.
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PDB codes:
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D.A.Lindhout,
and
B.D.Sykes
(2003).
Structure and dynamics of the C-domain of human cardiac troponin C in complex with the inhibitory region of human cardiac troponin I.
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J Biol Chem,
278,
27024-27034.
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PDB code:
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F.F.Valencia,
A.A.Paulucci,
R.B.Quaggio,
A.C.Da Silva,
C.S.Farah,
and
F.C.Reinach
(2003).
Parallel measurement of Ca2+ binding and fluorescence emission upon Ca2+ titration of recombinant skeletal muscle troponin C. Measurement of sequential calcium binding to the regulatory sites.
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J Biol Chem,
278,
11007-11014.
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F.Pitici
(2003).
Structural preference for changes in the direction of the Ca2+-induced transition: a study of the regulatory domain of skeletal troponin-C.
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Biophys J,
84,
82.
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S.B.Tikunova,
J.A.Rall,
and
J.P.Davis
(2002).
Effect of hydrophobic residue substitutions with glutamine on Ca(2+) binding and exchange with the N-domain of troponin C.
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Biochemistry,
41,
6697-6705.
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X.Wang,
M.X.Li,
and
B.D.Sykes
(2002).
Structure of the regulatory N-domain of human cardiac troponin C in complex with human cardiac troponin I147-163 and bepridil.
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J Biol Chem,
277,
31124-31133.
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PDB code:
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A.Ababou,
and
J.R.Desjarlais
(2001).
Solvation energetics and conformational change in EF-hand proteins.
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Protein Sci,
10,
301-312.
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B.V.Reddy,
W.W.Li,
I.N.Shindyalov,
and
P.E.Bourne
(2001).
Conserved key amino acid positions (CKAAPs) derived from the analysis of common substructures in proteins.
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Proteins,
42,
148-163.
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T.Kesvatera,
B.Jönsson,
E.Thulin,
and
S.Linse
(2001).
Focusing of the electrostatic potential at EF-hands of calbindin D(9k): titration of acidic residues.
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Proteins,
45,
129-135.
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D.H.MacLennan
(2000).
Ca2+ signalling and muscle disease.
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Eur J Biochem,
267,
5291-5297.
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R.Oliva,
L.Falcigno,
G.D'Auria,
M.Saviano,
L.Paolillo,
G.Ansanelli,
and
G.Zanotti
(2000).
Bicyclic peptides as models of calcium binding sites: synthesis and conformation of a homodetic undecapeptide.
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Biopolymers,
53,
581-595.
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Y.Li,
M.L.Love,
J.A.Putkey,
and
C.Cohen
(2000).
Bepridil opens the regulatory N-terminal lobe of cardiac troponin C.
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Proc Natl Acad Sci U S A,
97,
5140-5145.
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PDB code:
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B.Whitehead,
M.Tessari,
A.Carotenuto,
P.M.van Bergen en Henegouwen,
and
G.W.Vuister
(1999).
The EH1 domain of Eps15 is structurally classified as a member of the S100 subclass of EF-hand-containing proteins.
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Biochemistry,
38,
11271-11277.
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PDB code:
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W.J.Dong,
J.Xing,
M.Villain,
M.Hellinger,
J.M.Robinson,
M.Chandra,
R.J.Solaro,
P.K.Umeda,
and
H.C.Cheung
(1999).
Conformation of the regulatory domain of cardiac muscle troponin C in its complex with cardiac troponin I.
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J Biol Chem,
274,
31382-31390.
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A.Malmendal,
J.Evenäs,
E.Thulin,
G.P.Gippert,
T.Drakenberg,
and
S.Forsén
(1998).
When size is important. Accommodation of magnesium in a calcium binding regulatory domain.
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J Biol Chem,
273,
28994-29001.
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J.Evenäs,
A.Malmendal,
E.Thulin,
G.Carlström,
and
S.Forsén
(1998).
Ca2+ binding and conformational changes in a calmodulin domain.
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Biochemistry,
37,
13744-13754.
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J.Evenäs,
A.Malmendal,
and
S.Forsén
(1998).
Calcium.
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Curr Opin Chem Biol,
2,
293-302.
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K.Julenius,
E.Thulin,
S.Linse,
and
B.E.Finn
(1998).
Hydrophobic core substitutions in calbindin D9k: effects on stability and structure.
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Biochemistry,
37,
8915-8925.
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K.Pääkkönen,
A.Annila,
T.Sorsa,
P.Pollesello,
C.Tilgmann,
I.Kilpeläinen,
P.Karisola,
I.Ulmanen,
and
T.Drakenberg
(1998).
Solution structure and main chain dynamics of the regulatory domain (Residues 1-91) of human cardiac troponin C.
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J Biol Chem,
273,
15633-15638.
|
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L.Spyracopoulos,
S.M.Gagné,
M.X.Li,
and
B.D.Sykes
(1998).
Dynamics and thermodynamics of the regulatory domain of human cardiac troponin C in the apo- and calcium-saturated states.
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Biochemistry,
37,
18032-18044.
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M.R.Nelson,
and
W.J.Chazin
(1998).
An interaction-based analysis of calcium-induced conformational changes in Ca2+ sensor proteins.
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Protein Sci,
7,
270-282.
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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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R.T.McKay,
J.R.Pearlstone,
D.C.Corson,
S.M.Gagné,
L.B.Smillie,
and
B.D.Sykes
(1998).
Structure and interaction site of the regulatory domain of troponin-C when complexed with the 96-148 region of troponin-I.
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Biochemistry,
37,
12419-12430.
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PDB code:
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S.P.Smith,
and
G.S.Shaw
(1998).
A novel calcium-sensitive switch revealed by the structure of human S100B in the calcium-bound form.
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Structure,
6,
211-222.
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PDB code:
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Y.Ohizumi,
K.Matsunaga,
K.Nakatani,
and
J.Kobayashi
(1998).
The powerful stimulatory action of 6-O-acetyl-9-methyl-7-bromoeudistomin D on the contractile protein system of rabbit skeletal muscle.
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Jpn J Pharmacol,
76,
113-116.
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L.Spyracopoulos,
M.X.Li,
S.K.Sia,
S.M.Gagné,
M.Chandra,
R.J.Solaro,
and
B.D.Sykes
(1997).
Calcium-induced structural transition in the regulatory domain of human cardiac troponin C.
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Biochemistry,
36,
12138-12146.
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PDB codes:
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S.K.Sia,
M.X.Li,
L.Spyracopoulos,
S.M.Gagné,
W.Liu,
J.A.Putkey,
and
B.D.Sykes
(1997).
Structure of cardiac muscle troponin C unexpectedly reveals a closed regulatory domain.
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J Biol Chem,
272,
18216-18221.
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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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