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PDBsum entry 1fi5

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protein metals links
Contractile protein PDB id
1fi5

 

 

 

 

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Contents
Protein chain
81 a.a. *
Metals
_CA ×2
* Residue conservation analysis
PDB id:
1fi5
Name: Contractile protein
Title: Nmr structure of thE C terminal domain of cardiac troponin c bound to the n terminal domain of cardiac troponin i.
Structure: Protein (troponin c). Chain: a. Fragment: residues 81 - 161. Engineered: yes
Source: Gallus gallus. Chicken. Organism_taxid: 9031. Organ: heart. Tissue: muscle. Cell: myocyte. Cellular_location: thin filament. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008.
NMR struc: 20 models
Authors: G.M.Gasmi-Seabrook,J.W.Howarth,N.Finley,E.Abusamhadneh,V.Gaponenko, R.M.Brito,R.J.Solaro,P.R.Rosevear
Key ref:
G.M.Gasmi-Seabrook et al. (1999). Solution structures of the C-terminal domain of cardiac troponin C free and bound to the N-terminal domain of cardiac troponin I. Biochemistry, 38, 8313-8322. PubMed id: 10387077 DOI: 10.1021/bi9902642
Date:
03-Aug-00     Release date:   23-Aug-00    
Supersedes: 1ggs
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P09860  (TNNC1_CHICK) -  Troponin C, slow skeletal and cardiac muscles from Gallus gallus
Seq:
Struc:
161 a.a.
81 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
DOI no: 10.1021/bi9902642 Biochemistry 38:8313-8322 (1999)
PubMed id: 10387077  
 
 
Solution structures of the C-terminal domain of cardiac troponin C free and bound to the N-terminal domain of cardiac troponin I.
G.M.Gasmi-Seabrook, J.W.Howarth, N.Finley, E.Abusamhadneh, V.Gaponenko, R.M.Brito, R.J.Solaro, P.R.Rosevear.
 
  ABSTRACT  
 
The N-terminal domain of cardiac troponin I (cTnI) comprising residues 33-80 and lacking the cardiac-specific amino terminus forms a stable binary complex with the C-terminal domain of cardiac troponin C (cTnC) comprising residues 81-161. We have utilized heteronuclear multidimensional NMR to assign the backbone and side-chain resonances of Ca2+-saturated cTnC(81-161) both free and bound to cTnI(33-80). No significant differences were observed between secondary structural elements determined for free and cTnI(33-80)-bound cTnC(81-161). We have determined solution structures of Ca2+-saturated cTnC(81-161) free and bound to cTnI(33-80). While the tertiary structure of cTnC(81-161) is qualitatively similar to that observed free in solution, the binding of cTnI(33-80) results mainly in an opening of the structure and movement of the loop region between helices F and G. Together, these movements provide the binding site for the N-terminal domain of cTnI. The putative binding site for cTnI(33-80) was determined by mapping amide proton and nitrogen chemical shift changes, induced by the binding of cTnI(33-80), onto the C-terminal cTnC structure. The binding interface for cTnI(33-80), as suggested from chemical shift changes, involves predominantly hydrophobic interactions located in the expanded hydrophobic pocket. The largest chemical shift changes were observed in the loop region connecting helices F and G. Inspection of available TnC sequences reveals that these residues are highly conserved, suggesting a common binding motif for the Ca2+/Mg2+-dependent interaction site in the TnC/TnI complex.
 

Literature references that cite this PDB file's key reference

  PubMed id Reference
19542563 I.M.Robertson, M.X.Li, and B.D.Sykes (2009).
Solution structure of human cardiac troponin C in complex with the green tea polyphenol, (-)-epigallocatechin 3-gallate.
  J Biol Chem, 284, 23012-23023.
PDB code: 2kdh
18162171 M.X.Li, I.M.Robertson, and B.D.Sykes (2008).
Interaction of cardiac troponin with cardiotonic drugs: a structural perspective.
  Biochem Biophys Res Commun, 369, 88-99.  
17099250 P.L.Engel, T.Kobayashi, B.Biesiadecki, J.Davis, S.Tikunova, S.Wu, and R.J.Solaro (2007).
Identification of a region of troponin I important in signaling cross-bridge-dependent activation of cardiac myofilaments.
  J Biol Chem, 282, 183-193.  
16080151 H.Chen, and H.X.Zhou (2005).
Prediction of interface residues in protein-protein complexes by a consensus neural network method: test against NMR data.
  Proteins, 61, 21-35.  
15711886 M.X.Li, X.Wang, and B.D.Sykes (2004).
Structural based insights into the role of troponin in cardiac muscle pathophysiology.
  J Muscle Res Cell Motil, 25, 559-579.  
15485824 N.L.Finley, and P.R.Rosevear (2004).
Introduction of negative charge mimicking protein kinase C phosphorylation of cardiac troponin I. Effects on cardiac troponin C.
  J Biol Chem, 279, 54833-54840.  
12840750 S.Takeda, A.Yamashita, K.Maeda, and Y.Maéda (2003).
Structure of the core domain of human cardiac troponin in the Ca(2+)-saturated form.
  Nature, 424, 35-41.
PDB codes: 1j1d 1j1e
12147696 A.Dvoretsky, E.M.Abusamhadneh, J.W.Howarth, and P.R.Rosevear (2002).
Solution structure of calcium-saturated cardiac troponin C bound to cardiac troponin I.
  J Biol Chem, 277, 38565-38570.
PDB code: 1la0
12207022 D.G.Ward, M.P.Cornes, and I.P.Trayer (2002).
Structural consequences of cardiac troponin I phosphorylation.
  J Biol Chem, 277, 41795-41801.  
11352734 M.B.Abbott, W.J.Dong, A.Dvoretsky, B.DaGue, R.M.Caprioli, H.C.Cheung, and P.R.Rosevear (2001).
Modulation of cardiac troponin C-cardiac troponin I regulatory interactions by the amino-terminus of cardiac troponin I.
  Biochemistry, 40, 5992-6001.  
10913289 M.X.Li, L.Spyracopoulos, N.Beier, J.A.Putkey, and B.D.Sykes (2000).
Interaction of cardiac troponin C with Ca(2+) sensitizer EMD 57033 and cardiac troponin I inhibitory peptide.
  Biochemistry, 39, 8782-8790.  
10715110 P.Mercier, M.X.Li, and B.D.Sykes (2000).
Role of the structural domain of troponin C in muscle regulation: NMR studies of Ca2+ binding and subsequent interactions with regions 1-40 and 96-115 of troponin I.
  Biochemistry, 39, 2902-2911.  
10792039 Y.Li, M.L.Love, J.A.Putkey, and C.Cohen (2000).
Bepridil opens the regulatory N-terminal lobe of cardiac troponin C.
  Proc Natl Acad Sci U S A, 97, 5140-5145.
PDB code: 1dtl
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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