Troponin C type 1

Troponin C type 1 (slow), also known as TNNC1, is a human gene.cite web | title = Entrez Gene: TNNC1 troponin C type 1 (slow)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7134| accessdate = ]

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References

Further reading

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*cite journal | author=Gomes AV, Potter JD |title=Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene. |journal=Mol. Cell. Biochem. |volume=263 |issue= 1-2 |pages= 99–114 |year= 2005 |pmid= 15524171 |doi=
*cite journal | author=Tomasselli AG, Hui JO, Adams L, "et al." |title=Actin, troponin C, Alzheimer amyloid precursor protein and pro-interleukin 1 beta as substrates of the protease from human immunodeficiency virus. |journal=J. Biol. Chem. |volume=266 |issue= 22 |pages= 14548–53 |year= 1991 |pmid= 1907279 |doi=
*cite journal | author=Schreier T, Kedes L, Gahlmann R |title=Cloning, structural analysis, and expression of the human slow twitch skeletal muscle/cardiac troponin C gene. |journal=J. Biol. Chem. |volume=265 |issue= 34 |pages= 21247–53 |year= 1991 |pmid= 2250022 |doi=
*cite journal | author=Gahlmann R, Wade R, Gunning P, Kedes L |title=Differential expression of slow and fast skeletal muscle troponin C. Slow skeletal muscle troponin C is expressed in human fibroblasts. |journal=J. Mol. Biol. |volume=201 |issue= 2 |pages= 379–91 |year= 1988 |pmid= 3166492 |doi=
*cite journal | author=Roher A, Lieska N, Spitz W |title=The amino acid sequence of human cardiac troponin-C. |journal=Muscle Nerve |volume=9 |issue= 1 |pages= 73–7 |year= 1986 |pmid= 3951483 |doi= 10.1002/mus.880090112
*cite journal | author=Grand RJ, Levine BA, Perry SV |title=Proton-magnetic-resonance studies on the interaction of rabbit skeletal-muscle troponin I with troponin C and actin. |journal=Biochem. J. |volume=203 |issue= 1 |pages= 61–8 |year= 1982 |pmid= 7103951 |doi=
*cite journal | author=Thierfelder L, Watkins H, MacRae C, "et al." |title=Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. |journal=Cell |volume=77 |issue= 5 |pages= 701–12 |year= 1994 |pmid= 8205619 |doi=
*cite journal | author=Jha PK, Leavis PC, Sarkar S |title=Interaction of deletion mutants of troponins I and T: COOH-terminal truncation of troponin T abolishes troponin I binding and reduces Ca2+ sensitivity of the reconstituted regulatory system. |journal=Biochemistry |volume=35 |issue= 51 |pages= 16573–80 |year= 1997 |pmid= 8987992 |doi= 10.1021/bi9622433
*cite journal | author=Song WJ, Van Keuren ML, Drabkin HA, "et al." |title=Assignment of the human slow twitch skeletal muscle/cardiac troponin C gene (TNNC1) to human chromosome 3p21.3-->3p14.3 using somatic cell hybrids. |journal=Cytogenet. Cell Genet. |volume=75 |issue= 1 |pages= 36–7 |year= 1997 |pmid= 8995486 |doi=
*cite journal | author=Takeda S, Kobayashi T, Taniguchi H, "et al." |title=Structural and functional domains of the troponin complex revealed by limited digestion. |journal=Eur. J. Biochem. |volume=246 |issue= 3 |pages= 611–7 |year= 1997 |pmid= 9219516 |doi=
*cite journal | author=Spyracopoulos L, Li MX, Sia SK, "et al." |title=Calcium-induced structural transition in the regulatory domain of human cardiac troponin C. |journal=Biochemistry |volume=36 |issue= 40 |pages= 12138–46 |year= 1997 |pmid= 9315850 |doi= 10.1021/bi971223d
*cite journal | author=Keane NE, Quirk PG, Gao Y, "et al." |title=The ordered phosphorylation of cardiac troponin I by the cAMP-dependent protein kinase--structural consequences and functional implications. |journal=Eur. J. Biochem. |volume=248 |issue= 2 |pages= 329–37 |year= 1997 |pmid= 9346285 |doi=
*cite journal | author=Stefancsik R, Jha PK, Sarkar S |title=Identification and mutagenesis of a highly conserved domain in troponin T responsible for troponin I binding: potential role for coiled coil interaction. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 3 |pages= 957–62 |year= 1998 |pmid= 9448267 |doi=
*cite journal | author=Vassylyev DG, Takeda S, Wakatsuki S, "et al." |title=Crystal structure of troponin C in complex with troponin I fragment at 2.3-A resolution. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 9 |pages= 4847–52 |year= 1998 |pmid= 9560191 |doi=
*cite journal | author=Redwood C, Lohmann K, Bing W, "et al." |title=Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein. |journal=Circ. Res. |volume=86 |issue= 11 |pages= 1146–52 |year= 2000 |pmid= 10850966 |doi=
*cite journal | author=Hoffmann B, Schmidt-Traub H, Perrot A, "et al." |title=First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy. |journal=Hum. Mutat. |volume=17 |issue= 6 |pages= 524 |year= 2001 |pmid= 11385718 |doi= 10.1002/humu.1143
*cite journal | author=Schmidtmann A, Lohmann K, Jaquet K |title=The interaction of the bisphosphorylated N-terminal arm of cardiac troponin I-A 31P-NMR study. |journal=FEBS Lett. |volume=513 |issue= 2-3 |pages= 289–93 |year= 2002 |pmid= 11904166 |doi=
*cite journal | author=Lindhout DA, Li MX, Schieve D, Sykes BD |title=Effects of T142 phosphorylation and mutation R145G on the interaction of the inhibitory region of human cardiac troponin I with the C-domain of human cardiac troponin C. |journal=Biochemistry |volume=41 |issue= 23 |pages= 7267–74 |year= 2002 |pmid= 12044157 |doi=
*cite journal | author=Wang X, Li MX, Sykes BD |title=Structure of the regulatory N-domain of human cardiac troponin C in complex with human cardiac troponin I147-163 and bepridil. |journal=J. Biol. Chem. |volume=277 |issue= 34 |pages= 31124–33 |year= 2002 |pmid= 12060657 |doi= 10.1074/jbc.M203896200
*cite journal | author=Li MX, Saude EJ, Wang X, "et al." |title=Kinetic studies of calcium and cardiac troponin I peptide binding to human cardiac troponin C using NMR spectroscopy. |journal=Eur. Biophys. J. |volume=31 |issue= 4 |pages= 245–56 |year= 2003 |pmid= 12122471 |doi= 10.1007/s00249-002-0227-1

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