Mutations that define the optimal half-site for binding yeast GCN4 activator protein and identify an ATF/CREB-like repressor that recognizes similar DNA sites
about
The structure of a CREB bZIP.somatostatin CRE complex reveals the basis for selective dimerization and divalent cation-enhanced DNA bindingThe Sko1p repressor and Gcn4p activator antagonistically modulate stress-regulated transcription in Saccharomyces cerevisiaeACR1, a yeast ATF/CREB repressor.Yap, a novel family of eight bZIP proteins in Saccharomyces cerevisiae with distinct biological functionsYeast SKO1 gene encodes a bZIP protein that binds to the CRE motif and acts as a repressor of transcription.Aca1 and Aca2, ATF/CREB activators in Saccharomyces cerevisiae, are important for carbon source utilization but not the response to stress.Stabilization of bzip peptides through incorporation of fluorinated aliphatic residues.Consensus and variant cAMP-regulated enhancers have distinct CREB-binding properties.Gcn4p, a master regulator of gene expression, is controlled at multiple levels by diverse signals of starvation and stress.Identification of cell cycle-regulated genes in fission yeastElectrostatic control of half-site spacing preferences by the cyclic AMP response element-binding protein CREB.Binding sites of different geometries for the 16-3 phage repressor.Curated collection of yeast transcription factor DNA binding specificity data reveals novel structural and gene regulatory insights.The role of a basic amino acid cluster in target site selection and non-specific binding of bZIP peptides to DNA.Determinants of half-site spacing preferences that distinguish AP-1 and ATF/CREB bZIP domainsUracil interference, a rapid and general method for defining protein-DNA interactions involving the 5-methyl group of thymines: the GCN4-DNA complex.Modeling DNA affinity landscape through two-round support vector regression with weighted degree kernels.Interaction of calicheamicin gamma1(I) and its related carbohydrates with DNA-protein complexes.Characterization of the ATF/CREB site and its complex with GCN4.Role of the conserved leucines in the leucine zipper dimerization motif of yeast GCN4.Design of a metallo-bZIP protein that discriminates between CRE and AP1 target sites: selection against AP1Adaptability at the protein-DNA interface is an important aspect of sequence recognition by bZIP proteins.DNA-binding specificity of the PAR basic leucine zipper protein VBP partially overlaps those of the C/EBP and CREB/ATF families and is influenced by domains that flank the core basic regionThe role of helix stabilizing residues in GCN4 basic region folding and DNA binding.Yeast intragenic transcriptional control: activation and repression sites within the coding region of the Saccharomyces cerevisiae LPD1 gene.Interspersion of an unusual GCN4 activation site with a complex transcriptional repression site in Ty2 elements of Saccharomyces cerevisiae.Identification of base and backbone contacts used for DNA sequence recognition and high-affinity binding by LAC9, a transcription activator containing a C6 zinc finger.Pheromone response elements are necessary and sufficient for basal and pheromone-induced transcription of the FUS1 gene of Saccharomyces cerevisiae.DNA binding specificity of the wheat bZIP protein EmBP-1Highly conserved residues in the bZIP domain of yeast GCN4 are not essential for DNA bindingIdentification of C/EBP basic region residues involved in DNA sequence recognition and half-site spacing preferenceMutations in the bZIP domain of yeast GCN4 that alter DNA-binding specificity.Three protein binding sites form an enhancer that regulates sex- and fat body-specific transcription of Drosophila yolk protein genes.Two distinct yeast transcriptional activators require the function of the GCN5 protein to promote normal levels of transcriptionGenetic analysis of the Tn21 mer operator-promoter.The human T-cell leukemia virus-1 transcriptional activator Tax enhances cAMP-responsive element-binding protein (CREB) binding activity through interactions with the DNA minor groove.PNA zipper as a dimerization tool: development of a bZip mimic.Design of a C/EBP-specific, dominant-negative bZIP protein with both inhibitory and gain-of-function properties.Sequence-specific recognition of DNA by hydrophobic, alanine-rich mutants of the basic region/leucine zipper motif investigated by fluorescence anisotropy.Metal-ion-regulated miniature DNA-binding proteins based on GCN4 and non-native regulation sites.
P2860
Q27626640-08CD11BF-6A95-48EC-A451-C15DD1B7CE9DQ27932201-D0D3E674-42C8-4EE7-B4F9-27A5A50ABD6EQ27932635-E347E370-C7C6-48F7-AD39-A121A6BB4B9FQ27932694-65C2DC92-DCAF-447F-92F6-08AB5E92CFEFQ27936314-FED2FE02-BDE2-41B1-803F-11A74C6C20E0Q27936425-278237D1-1007-4513-AB75-7AC73A548E54Q30354827-A191713A-EF08-49E4-999D-ADE4E8EB7368Q31779561-D15D31E7-8F28-422B-8CFD-3DB8C678A60BQ33905702-6940C784-895F-49AB-B435-CA1ABFA63EF9Q33913568-394D1E35-FF08-4F20-A335-BC0C02865E08Q33941405-258301C5-743D-469E-A68F-22A854C87BD3Q34065961-F6184AFE-2363-4D3B-A89A-605C22EF4E5BQ34107923-A54778D3-B83D-4E36-B629-4FBE905BB311Q34633134-D5BDF572-F192-466C-A7CD-945699E18820Q34761102-D43D6960-CA0E-4E78-BF15-E40280D2ABB0Q35060086-197E3D41-8AEB-4902-A328-E1D04C3F77CCQ35545692-6CBFDAB7-F61C-42BC-AEA4-E48CFBF300D4Q35627787-0F9EE7AE-A5DA-4626-823F-3DCC1EDE071AQ35861327-998FEB71-A7CF-4FBA-8EA1-1B34909F41F6Q35922443-CAD60EBF-0759-4625-8258-D4909F44713FQ36093527-FACE3A99-E2F2-4E94-A768-AF5F43C0C7CAQ36302373-1CA2445F-4B3F-4D60-8EB6-3FDC9B4791D3Q36550283-9FB8E1F6-BC7A-4FF9-9FA8-7BA6AFDD1B4DQ36639578-DEB11374-914D-4F68-B01D-002D16EA080EQ36643139-95A555AC-8947-4237-9953-A3E2CDAAE0D5Q36677681-46365482-B3AB-4855-827E-F2F817727C7DQ36687052-3C787350-311B-4DAE-8941-CC4A11D63848Q36695111-4CF18CD8-492D-4D6F-8C24-AC694529E2FAQ36709983-573ABB2D-DE7C-4C11-8DD3-42214E2A9393Q36735327-8D32B5F3-8C77-4DBA-9409-F4F708BA6F6BQ36825593-DE312842-363E-40BE-BF6A-A974E869FBFBQ36874608-33E93F7D-8C8B-403B-937E-4B33F39B32F7Q37695186-75616719-932D-42A6-B992-F9D63F597EA7Q38324867-84710C1B-001E-4FB0-85C8-04D11DA48F5CQ38329797-ED55233E-74DE-452E-B6BD-15DC3B5B1F2AQ38335455-FDE83FE5-1B51-4C6E-A2EB-751D141D803EQ38348615-BB69AA34-916C-44A3-BB6C-2C0B9532E9D5Q38362528-B73F20BB-9986-4070-9597-2F082EAC1C60Q38363364-0EE0F71E-8503-4BC3-BFD0-AE8DC1A6E7F2Q39260495-3C76FD20-E506-4021-B3AC-9E633360F7D3
P2860
Mutations that define the optimal half-site for binding yeast GCN4 activator protein and identify an ATF/CREB-like repressor that recognizes similar DNA sites
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Mutations that define the opti ...... t recognizes similar DNA sites
@ast
Mutations that define the opti ...... t recognizes similar DNA sites
@en
Mutations that define the opti ...... recognizes similar DNA sites.
@nl
type
label
Mutations that define the opti ...... t recognizes similar DNA sites
@ast
Mutations that define the opti ...... t recognizes similar DNA sites
@en
Mutations that define the opti ...... recognizes similar DNA sites.
@nl
prefLabel
Mutations that define the opti ...... t recognizes similar DNA sites
@ast
Mutations that define the opti ...... t recognizes similar DNA sites
@en
Mutations that define the opti ...... recognizes similar DNA sites.
@nl
P2093
P2860
P356
P1476
Mutations that define the opti ...... t recognizes similar DNA sites
@en
P2093
A C Vincent
J W Sellers
P2860
P304
P356
10.1128/MCB.10.10.5077
P407
P577
1990-10-01T00:00:00Z