Biological function and site II Ca2+-induced opening of the regulatory domain of skeletal troponin C are impaired by invariant site I or II Glu mutations.
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Calcium induced regulation of skeletal troponin--computational insights from molecular dynamics simulationsGenetically encoded indicators of cellular calcium dynamics based on troponin C and green fluorescent proteinTroponin C isoform composition determines differences in Sr(2+)-activation characteristics between rat diaphragm fibersMicrotiter plate monoclonal antibody epitope analysis of Ca2+- and Mg2+-induced conformational changes in troponin C.Predicting cardiomyopathic phenotypes by altering Ca2+ affinity of cardiac troponin C.Measurement of calcium dissociation rates from troponin C in rigor skeletal myofibrils.Structural and functional consequences of the cardiac troponin C L48Q Ca(2+)-sensitizing mutation.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.The structural and functional effects of the familial hypertrophic cardiomyopathy-linked cardiac troponin C mutation, L29QEffects of Phe-to-Trp mutation and fluorotryptophan incorporation on the solution structure of cardiac troponin C, and analysis of its suitability as a potential probe for in situ NMR studiesThe Dictyostelium class I myosin, MyoD, contains a novel light chain that lacks high-affinity calcium-binding sites.
P2860
Q27335224-E6D5BE8A-8AFC-4AB4-93EE-2BA151627EE7Q28240511-4299C4FE-55F4-4FDD-A14E-9FCE4587ECF0Q28566228-71AD4C7E-9C54-4488-A68D-35E6E875347AQ30363923-D2692746-06B1-435F-8D95-92D330F186A3Q34107285-1E16E1CE-CAAC-4456-AB6F-C507F732A5AFQ35302171-8254DA75-3767-4AA1-B912-2DF7E0DEE7F7Q36219998-7F5FFBB5-DC2A-420A-A059-F66D56F30CF3Q38358578-3F8F7004-8865-4213-B714-07B244D5AA61Q40572286-C638C69A-643F-4F86-BA36-2A4BC03FFD91Q42137052-A69B7745-1F00-4AFC-B3BA-88C4689B1C3EQ42157088-B63B56AD-C3AA-4B29-A371-AAD46C957DC7
P2860
Biological function and site II Ca2+-induced opening of the regulatory domain of skeletal troponin C are impaired by invariant site I or II Glu mutations.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Biological function and site I ...... nt site I or II Glu mutations.
@en
Biological function and site I ...... nt site I or II Glu mutations.
@nl
type
label
Biological function and site I ...... nt site I or II Glu mutations.
@en
Biological function and site I ...... nt site I or II Glu mutations.
@nl
prefLabel
Biological function and site I ...... nt site I or II Glu mutations.
@en
Biological function and site I ...... nt site I or II Glu mutations.
@nl
P2093
P2860
P356
P1476
Biological function and site I ...... nt site I or II Glu mutations.
@en
P2093
Pearlstone JR
Smillie LB
Sorenson MM
P2860
P304
35106-35115
P356
10.1074/JBC.M001000200
P407
P577
2000-11-01T00:00:00Z