A component of excitation-contraction coupling triggered in the absence of the T671-L690 and L720-Q765 regions of the II-III loop of the dihydropyridine receptor alpha(1s) pore subunit.
about
Functional analysis of a frame-shift mutant of the dihydropyridine receptor pore subunit (alpha1S) expressing two complementary protein fragmentsCa(V)1.1: The atypical prototypical voltage-gated Ca²⁺ channelScorpion venom components that affect ion-channels functionLooking for answers to EC coupling's persistent questionsTruncation of the carboxyl terminus of the dihydropyridine receptor beta1a subunit promotes Ca2+ dependent excitation-contraction coupling in skeletal myotubes.Ca2+ current and charge movements in skeletal myotubes promoted by the beta-subunit of the dihydropyridine receptor in the absence of ryanodine receptor type 1.Ca2+-dependent excitation-contraction coupling triggered by the heterologous cardiac/brain DHPR beta2a-subunit in skeletal myotubesInvolvement of a heptad repeat in the carboxyl terminus of the dihydropyridine receptor beta1a subunit in the mechanism of excitation-contraction coupling in skeletal muscleFunctional interaction of CaV channel isoforms with ryanodine receptors studied in dysgenic myotubesInteraction between the dihydropyridine receptor Ca2+ channel beta-subunit and ryanodine receptor type 1 strengthens excitation-contraction couplingMultiple loops of the dihydropyridine receptor pore subunit are required for full-scale excitation-contraction coupling in skeletal muscle.Transient loss of voltage control of Ca2+ release in the presence of maurocalcine in skeletal muscle.Functional implications of modifying RyR-activating peptides for membrane permeability.Cyclization of the intrinsically disordered α1S dihydropyridine receptor II-III loop enhances secondary structure and in vitro function.Accessibility of targeted DHPR sites to streptavidin and functional effects of binding on EC coupling.Effects of inserting fluorescent proteins into the alpha1S II-III loop: insights into excitation-contraction coupling.Ryanoids and imperatoxin affect the modulation of cardiac ryanodine receptors by dihydropyridine receptor Peptide A.The IQ motif is crucial for Cav1.1 functionStructural requirements of the dihydropyridine receptor alpha1S II-III loop for skeletal-type excitation-contraction coupling.Effects of peptide C corresponding to the Glu724-Pro760 region of the II-III loop of the DHP (dihydropyridine) receptor alpha1 subunit on the domain- switch-mediated activation of RyR1 (ryanodine receptor 1) Ca2+ channels.The alpha(1S) III-IV loop influences 1,4-dihydropyridine receptor gating but is not directly involved in excitation-contraction coupling interactions with the type 1 ryanodine receptor.The recombinant dihydropyridine receptor II-III loop and partly structured 'C' region peptides modify cardiac ryanodine receptor activity.The random-coil 'C' fragment of the dihydropyridine receptor II-III loop can activate or inhibit native skeletal ryanodine receptors.Peptide fragments of the dihydropyridine receptor can modulate cardiac ryanodine receptor channel activity and sarcoplasmic reticulum Ca2+ release.Critical amino acid residues determine the binding affinity and the Ca2+ release efficacy of maurocalcine in skeletal muscle cells.Multiple actions of imperatoxin A on ryanodine receptors: interactions with the II-III loop "A" fragment.
P2860
Q24798316-2515D4D5-B0F8-46C0-97C3-C149CFB293B2Q26866428-12DFF1F1-7315-4490-84F3-56D6898F564AQ33871187-92991363-873C-41E5-BBAE-A7786BE03EB5Q33950677-2876AA78-E54A-425A-9214-DB0A6432FCA1Q34180090-730676EF-E9B1-468A-85B3-A7C89CF0A224Q34180386-0C8C1F67-76F7-4477-89B2-99D5F8852EAAQ34183948-80743749-0D50-4882-B62C-ED86DFC8F24CQ34186764-EEACFA47-896A-4B9C-AECD-B8EB758D0CCDQ34189364-D04FF021-9A18-4A9F-8A6B-1243313F7BF6Q34244881-AA55C625-8876-4ABB-AABA-50A24CC28F3DQ34350397-2AB12770-C27B-4E45-85C6-094B7326762DQ35012286-43AF20D9-F1DE-41BF-BFB1-3C81CDC8BA1CQ35048695-E7D32176-8D97-4DE6-9802-997BED93DE43Q35063164-657A546B-6208-422C-A0D0-F679A4576EFAQ36296090-A8C7B353-155E-425B-B1BB-DED1FE7114DDQ37267658-04276994-364C-4AC6-BB17-1680967EEC7EQ37334686-C7E558D6-BF60-45B0-94A5-6CDFF3B74C08Q39522381-ABC48004-3DD9-4DCA-BF10-B547AB55B248Q40615240-C81E8B2D-E369-4A12-9C20-86503D0BB136Q41806986-758171F9-0A7F-4A54-BBD0-6759BDDEA9B4Q41992939-71DE1D4E-6B08-45B9-A1B2-EB11FE4005F3Q42814147-E0D46C5D-8C4B-42D9-9D7F-788AED81E1BAQ43002889-D4769EEB-EBC9-44AC-97C6-50D02EC91852Q43003629-7B76F94B-CC91-4321-92A7-03C3DAFC6D1EQ44517508-DC16E83B-734A-44FD-865D-7C3A8AA3BA04Q44709105-857D4560-5D0A-4278-9D51-47B4B612983E
P2860
A component of excitation-contraction coupling triggered in the absence of the T671-L690 and L720-Q765 regions of the II-III loop of the dihydropyridine receptor alpha(1s) pore subunit.
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
A component of excitation-cont ...... eceptor alpha(1s) pore subunit
@nl
A component of excitation-cont ...... ceptor alpha(1s) pore subunit.
@ast
A component of excitation-cont ...... ceptor alpha(1s) pore subunit.
@en
type
label
A component of excitation-cont ...... eceptor alpha(1s) pore subunit
@nl
A component of excitation-cont ...... ceptor alpha(1s) pore subunit.
@ast
A component of excitation-cont ...... ceptor alpha(1s) pore subunit.
@en
prefLabel
A component of excitation-cont ...... eceptor alpha(1s) pore subunit
@nl
A component of excitation-cont ...... ceptor alpha(1s) pore subunit.
@ast
A component of excitation-cont ...... ceptor alpha(1s) pore subunit.
@en
P2093
P2860
P1433
P1476
A component of excitation-cont ...... eceptor alpha(1s) pore subunit
@en
P2093
D Bhattacharya
L Mortenson
R Coronado
P2860
P304
P356
10.1016/S0006-3495(01)75963-2
P407
P577
2001-12-01T00:00:00Z