X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
about
Btf, a novel death-promoting transcriptional repressor that interacts with Bcl-2-related proteins.Bax oligomerization is required for channel-forming activity in liposomes and to trigger cytochrome c release from mitochondriaStructural basis of BFL-1 for its interaction with BAX and its anti-apoptotic action in mammalian and yeast cellstBID, a membrane-targeted death ligand, oligomerizes BAK to release cytochrome cMAP-1, a novel proapoptotic protein containing a BH3-like motif that associates with Bax through its Bcl-2 homology domainsBcl-rambo, a novel Bcl-2 homologue that induces apoptosis via its unique C-terminal extensionTumor necrosis factor-alpha induces Bax-Bak interaction and apoptosis, which is inhibited by adenovirus E1B 19KtBid undergoes multiple conformational changes at the membrane required for Bax activationc-Abl tyrosine kinase regulates the human Rad9 checkpoint protein in response to DNA damagePrevention of cytokine withdrawal-induced apoptosis by Mcl-1 requires interaction between Mcl-1 and BimFunctional and structural studies of the vaccinia virus virulence factor N1 reveal a Bcl-2-like anti-apoptotic proteinStructural changes in the BH3 domain of SOUL protein upon interaction with the anti-apoptotic protein Bcl-xLThe conserved N-terminal BH4 domain of Bcl-2 homologues is essential for inhibition of apoptosis and interaction with CED-4Dimerization properties of human BAD. Identification of a BH-3 domain and analysis of its binding to mutant BCL-2 and BCL-XL proteinsBAG-1 modulates the chaperone activity of Hsp70/Hsc70.A common binding site mediates heterodimerization and homodimerization of Bcl-2 family membersVaccinia virus N1L protein resembles a B cell lymphoma-2 (Bcl-2) family proteinVaccinia virus anti-apoptotic F1L is a novel Bcl-2-like domain-swapped dimer that binds a highly selective subset of BH3-containing death ligandsBcl-xL phosphorylation at Ser49 by polo kinase 3 during cell cycle progression and checkpointsMutation to Bax beyond the BH3 domain disrupts interactions with pro-survival proteins and promotes apoptosisIdentification of novel in vivo phosphorylation sites of the human proapoptotic protein BAD: pore-forming activity of BAD is regulated by phosphorylationMAP-1 is a mitochondrial effector of Bax.Bim: a novel member of the Bcl-2 family that promotes apoptosisEnforced dimerization of BAX results in its translocation, mitochondrial dysfunction and apoptosisConformation of the Bax C-terminus regulates subcellular location and cell deathActivation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix.Microtubule-targeting drugs induce Bcl-2 phosphorylation and association with Pin1Microtubule-targeting drugs induce bcl-2 phosphorylation and association with Pin1Structural analysis of an eIF3 subcomplex reveals conserved interactions required for a stable and proper translation pre-initiation complex assemblyBcl-2 inhibitors: targeting mitochondrial apoptotic pathways in cancer therapySmall-molecule Bcl-2 antagonists as targeted therapy in oncologyCytosol-to-membrane redistribution of Bax and Bcl-X(L) during apoptosisRationale for Bcl-xL/Bad peptide complex formation from structure, mutagenesis, and biophysical studiesProapoptotic BH3-only proteins trigger membrane integration of prosurvival Bcl-w and neutralize its activityBH4 domain of antiapoptotic Bcl-2 family members closes voltage-dependent anion channel and inhibits apoptotic mitochondrial changes and cell deathEvidence that membrane insertion of the cytosolic domain of Bcl-xL is governed by an electrostatic mechanismThe structure of Bcl-w reveals a role for the C-terminal residues in modulating biological activityA surface groove essential for viral Bcl-2 function during chronic infection in vivo.Asparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis)The role of BH3-mimetic drugs in the treatment of pediatric hepatoblastoma
P2860
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P2860
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
description
1996 nî lūn-bûn
@nan
1996 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@ast
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@en
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@nl
type
label
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@ast
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@en
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@nl
prefLabel
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@ast
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@en
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@nl
P2093
P3181
P356
P1433
P1476
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
@en
P2093
C B Thompson
D Nettesheim
J E Harlan
R P Meadows
P2888
P304
P3181
P356
10.1038/381335A0
P407
P577
1996-05-23T00:00:00Z
P6179
1003038902