A unique structure at the carboxyl terminus of the largest subunit of eukaryotic RNA polymerase II.
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A serine/arginine-rich nuclear matrix cyclophilin interacts with the C-terminal domain of RNA polymerase IIFunctional studies of the carboxy-terminal repeat domain of Drosophila RNA polymerase II in vivoSplicing and transcription-associated proteins PSF and p54nrb/nonO bind to the RNA polymerase II CTDCerebellar degeneration-related antigen: a highly conserved neuroectodermal marker mapped to chromosomes X in human and mouseRole of the C-terminal domain of RNA polymerase II in U2 snRNA transcription and 3' processingCloning of a brain protein identified by autoantibodies from a patient with paraneoplastic cerebellar degenerationThe translocation (6;9), associated with a specific subtype of acute myeloid leukemia, results in the fusion of two genes, dek and can, and the expression of a chimeric, leukemia-specific dek-can mRNAA protein kinase that phosphorylates the C-terminal repeat domain of the largest subunit of RNA polymerase IIA human primary T-lymphocyte-derived human immunodeficiency virus type 1 Tat-associated kinase phosphorylates the C-terminal domain of RNA polymerase II and induces CAK activityLentivirus Tat proteins specifically associate with a cellular protein kinase, TAK, that hyperphosphorylates the carboxyl-terminal domain of the large subunit of RNA polymerase II: candidate for a Tat cofactorComparative genomics of cyclin-dependent kinases suggest co-evolution of the RNAP II C-terminal domain and CTD-directed CDKsTransition from initiation to promoter proximal pausing requires the CTD of RNA polymerase IIDeterminants for Dephosphorylation of the RNA Polymerase II C-Terminal Domain by Scp1Structural genomics of protein phosphatasesThe transcriptional coactivator PC4/Sub1 has multiple functions in RNA polymerase II transcription.Bur1 kinase is required for efficient transcription elongation by RNA polymerase II.The ESS1 prolyl isomerase and its suppressor BYE1 interact with RNA pol II to inhibit transcription elongation in Saccharomyces cerevisiae.Intragenic and extragenic suppressors of mutations in the heptapeptide repeat domain of Saccharomyces cerevisiae RNA polymerase IICTD kinase large subunit is encoded by CTK1, a gene required for normal growth of Saccharomyces cerevisiae.A motif shared by TFIIF and TFIIB mediates their interaction with the RNA polymerase II carboxy-terminal domain phosphatase Fcp1p in Saccharomyces cerevisiaeYeast RPO41 gene product is required for transcription and maintenance of the mitochondrial genomeFcp1 directly recognizes the C-terminal domain (CTD) and interacts with a site on RNA polymerase II distinct from the CTD.KIN28 encodes a C-terminal domain kinase that controls mRNA transcription in Saccharomyces cerevisiae but lacks cyclin-dependent kinase-activating kinase (CAK) activity.Kin28, the TFIIH-associated carboxy-terminal domain kinase, facilitates the recruitment of mRNA processing machinery to RNA polymerase II.Transcription elongation factor SII interacts with a domain of the large subunit of human RNA polymerase IICyclin C/CDK8 and cyclin H/CDK7/p36 are biochemically distinct CTD kinasesTranscriptional activators control splicing and 3'-end cleavage levelsA nuclear matrix protein interacts with the phosphorylated C-terminal domain of RNA polymerase II.The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteinsAffinity purification of mammalian RNA polymerase I. Identification of an associated kinase5'-Capping enzymes are targeted to pre-mRNA by binding to the phosphorylated carboxy-terminal domain of RNA polymerase IISelective constraint and the evolution of the RNA polymerase II C-Terminal DomainRNA Polymerase II C-Terminal Domain: Tethering Transcription to Transcript and TemplateTwo novel genes expressed in Xenopus germ line: characteristic features of putative protein structures, their gene expression profiles and their possible roles in gametogenesis and embryogenesis.Phosphorylation-regulated binding of RNA polymerase II to fibrous polymers of low-complexity domains.The Trypanosoma cruzi neuraminidase contains sequences similar to bacterial neuraminidases, YWTD repeats of the low density lipoprotein receptor, and type III modules of fibronectinThe non-canonical CTD of RNAP-II is essential for productive RNA synthesis in Trypanosoma brucei.Yeast upstream activator protein GCN4 can stimulate transcription when its binding site replaces the TATA elementThe C-terminal repeat domain of RNA polymerase II largest subunit is essential in vivo but is not required for accurate transcription initiation in vitroTwo mouse genes encoding potential transcription factors with identical DNA-binding domains are activated by growth factors in cultured cells.
P2860
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P2860
A unique structure at the carboxyl terminus of the largest subunit of eukaryotic RNA polymerase II.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 1985
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@en
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@nl
type
label
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@en
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@nl
prefLabel
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@en
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@nl
P2093
P2860
P356
P1476
A unique structure at the carb ...... eukaryotic RNA polymerase II.
@en
P2093
D L Cadena
J L Corden
J M Ahearn
M E Dahmus
P2860
P304
P356
10.1073/PNAS.82.23.7934
P407
P577
1985-12-01T00:00:00Z