XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations
about
SF1 and SF2 helicases: family mattersXeroderma pigmentosum and other diseases of human premature aging and DNA repair: molecules to patientsSubunit architecture of general transcription factor TFIIHThe helicase XPD unwinds bubble structures and is not stalled by DNA lesions removed by the nucleotide excision repair pathwayXeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulationMetals in biology: defining metalloproteomesDisease-causing missense mutations in human DNA helicase disordersDouble strand binding-single strand incision mechanism for human flap endonuclease: implications for the superfamilyNucleotide excision repair in eukaryotesStructure of an RNA polymerase II preinitiation complex.Taking a molecular motor for a spin: helicase mechanism studied by spin labeling and PELDOR.Emerging critical roles of Fe-S clusters in DNA replication and repair.Mre11 Dimers Coordinate DNA End Bridging and Nuclease Processing in Double-Strand-Break RepairSuperoxide dismutase from the eukaryotic thermophile Alvinella pompejana: structures, stability, mechanism, and insights into amyotrophic lateral sclerosisNbs1 Flexibly Tethers Ctp1 and Mre11-Rad50 to Coordinate DNA Double-Strand Break Processing and RepairInsights into eukaryotic DNA priming from the structure and functional interactions of the 4Fe-4S cluster domain of human DNA primaseFunctional and structural studies of the nucleotide excision repair helicase XPD suggest a polarity for DNA translocationEukaryotic Class II Cyclobutane Pyrimidine Dimer Photolyase Structure Reveals Basis for Improved Ultraviolet Tolerance in PlantsInsights into Chi recognition from the structure of an AddAB-type helicase-nuclease complexStructure of the C-terminal half of human XPB helicase and the impact of the disease-causing mutation XP11BEFunction of Conserved Topological Regions within the Saccharomyces cerevisiae Basal Transcription Factor TFIIHPlasmodium falciparum XPD translocates in 5' to 3' direction, is expressed throughout the blood stages, and interacts with p44Involvement of Iron-Containing Proteins in Genome Integrity in Arabidopsis ThalianaEnvisioning the dynamics and flexibility of Mre11-Rad50-Nbs1 complex to decipher its roles in DNA replication and repairNear-atomic resolution visualization of human transcription promoter opening.Physiological consequences of defects in ERCC1-XPF DNA repair endonucleaseDeveloping advanced X-ray scattering methods combined with crystallography and computationThe CIA Targeting Complex Is Highly Regulated and Provides Two Distinct Binding Sites for Client Iron-Sulfur Proteins.Actin dosage lethality screening in yeast mediated by selective ploidy ablation reveals links to urmylation/wobble codon recognition and chromosome stability.Single-molecule analysis reveals differential effect of ssDNA-binding proteins on DNA translocation by XPD helicaseImplementation and performance of SIBYLS: a dual endstation small-angle X-ray scattering and macromolecular crystallography beamline at the Advanced Light Source.Architecture of the Human and Yeast General Transcription and DNA Repair Factor TFIIHA unified model for the molecular basis of Xeroderma pigmentosum-Cockayne Syndrome.G quadruplexes are genomewide targets of transcriptional helicases XPB and XPD.Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients.Mechanistic and biological aspects of helicase action on damaged DNA.Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutationsBridging the solution divide: comprehensive structural analyses of dynamic RNA, DNA, and protein assemblies by small-angle X-ray scattering.Predicting protein-DNA interactions by full search computational docking.Fast protein folding kinetics
P2860
Q24596016-A82819A6-9B23-41A5-A5DE-2A89826A1A49Q24628121-9FA57192-7488-4844-9726-98844E19BBAEQ24633293-14BDB5C6-577D-4EEE-9453-7E6A3492D065Q24652700-6E20622E-7ECE-4A5A-8CF2-B3E1AD291744Q26777633-F5E0E98F-C341-4B39-81D1-82610B402521Q26822635-F038B6DD-872B-4A45-959E-A3B2927FEC71Q26828898-FA7CF28A-AF9F-4B84-9B1D-4ADA9394BBEDQ26850039-1FFA8DA8-91D4-4C97-B2EA-9E56DFF4C2C4Q26850656-BAB8CFF7-D536-4994-84F7-5B8D46BFD6F7Q27318217-676EB91C-4E0C-4C58-9FBC-E394413FD643Q27324828-082C0E2E-9330-4625-9CE6-038FC2875F43Q27332013-34E414ED-8E68-4B6C-89D1-1B896D26EA5BQ27652502-9F2E505F-F092-4ACF-A611-120E187A31E2Q27653085-127906BF-29FA-4E64-B230-7DBD4CA55795Q27657670-1F78A09C-62C4-47AB-B5C1-4F191C4168AEQ27663575-D71354E9-AA19-4400-A2A7-20A78D328F8FQ27675554-23CC6898-735C-491C-9784-FCC759170A66Q27676183-06CB4950-68D3-4253-AF10-7A7E8DFAFE7AQ27677071-6DD7B091-4B91-4345-89A5-13787197593FQ27683946-52686504-1F99-468D-894B-5B11C0E0BC14Q27930595-9A69A1FA-BDF2-438D-B090-70E4C212D25AQ27973474-F4D7C3B8-B059-4722-8606-7213C3EDF6CAQ28084415-89BB9F5F-40DD-4177-A84D-E5D18DDA7775Q28085622-E6ADE837-AFF6-4C34-A95D-C6DC83CC693AQ28114858-007E95BC-8844-4F30-8665-2009C5E4A71AQ28238547-AF738AF6-5F39-4A15-83D0-37783026F9B7Q28681355-5CBA8EB5-F5CB-4BC9-8EA0-24C8975E3E74Q29568899-166F13E0-1B6C-4076-83A6-007189210627Q30422154-CC84FACF-B8DE-4567-A12E-C0BBB7AF497BQ30491608-A4D81835-51AA-4B91-96D6-26D2B7C0D306Q30532509-27564B27-67FC-4C14-B596-1D1CEF770686Q33285675-4C1A4E94-2993-43D8-9E6B-7D83B4AB4BF6Q33361700-7FC7B3E2-287D-454A-9B6C-86E066C2F322Q33551414-8208BD55-CE5E-4D68-A7BA-1CE3C576D694Q33590419-5A495B47-B685-4C17-95A8-5567F40BF992Q33614603-98888352-160F-4511-A205-13E8B2516A08Q33675765-BC5DECC8-C20E-45EA-9ADF-4D67C838D330Q33693367-F0690576-5CBC-474E-892C-AEF1BBAD2CD9Q33712176-475795E9-DA43-47EE-A361-907FF019EBADQ33719314-2F357846-D8AA-4283-88B6-61CBBC31FFA8
P2860
XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
XPD helicase structures and ac ...... phenotypes from XPD mutations
@ast
XPD helicase structures and ac ...... phenotypes from XPD mutations
@en
XPD helicase structures and ac ...... phenotypes from XPD mutations
@nl
type
label
XPD helicase structures and ac ...... phenotypes from XPD mutations
@ast
XPD helicase structures and ac ...... phenotypes from XPD mutations
@en
XPD helicase structures and ac ...... phenotypes from XPD mutations
@nl
altLabel
XPD Helicase Structures and Ac ...... Phenotypes from XPD Mutations
@en
prefLabel
XPD helicase structures and ac ...... phenotypes from XPD mutations
@ast
XPD helicase structures and ac ...... phenotypes from XPD mutations
@en
XPD helicase structures and ac ...... phenotypes from XPD mutations
@nl
P2093
P2860
P3181
P1433
P1476
XPD helicase structures and ac ...... phenotypes from XPD mutations
@en
P2093
Andrew S Arvai
Jill O Fuss
John A Tainer
Priscilla K Cooper
Quen J Cheng
Victoria A Roberts
P2860
P304
P3181
P356
10.1016/J.CELL.2008.04.030
P407
P577
2008-05-30T00:00:00Z