| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Maria Miller | |
| P2860 | cites work | The role of human MBF1 as a transcriptional coactivator | Q22010815 |
| Intrinsically unstructured proteins and their functions | Q22061731 | ||
| Prediction and Functional Analysis of Native Disorder in Proteins from the Three Kingdoms of Life | Q22061741 | ||
| A practical overview of protein disorder prediction methods | Q22061753 | ||
| Divergent hTAFII31-binding motifs hidden in activation domains | Q22254120 | ||
| TORCs: transducers of regulated CREB activity | Q24297430 | ||
| The BRCT Domain Is a Phospho-Protein Binding Domain | Q24298428 | ||
| The proto-oncogene HLF and the related basic leucine zipper protein TEF display highly similar DNA-binding and transcriptional regulatory properties | Q24313204 | ||
| Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain | Q24314763 | ||
| Structural basis for recruitment of CBP/p300 by hypoxia-inducible factor-1 alpha | Q24534120 | ||
| CCAAT/enhancer-binding proteins: structure, function and regulation | Q24534323 | ||
| Classification of human B-ZIP proteins based on dimerization properties | Q24540084 | ||
| Alternative splicing in concert with protein intrinsic disorder enables increased functional diversity in multicellular organisms | Q24548466 | ||
| c-Fos-induced activation of a TATA-box-containing promoter involves direct contact with TATA-box-binding protein | Q24609940 | ||
| ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins | Q24672414 | ||
| JunB potentiates function of BRCA1 activation domain 1 (AD1) through a coiled-coil-mediated interaction | Q24675100 | ||
| Analysis of the structural properties of cAMP-responsive element-binding protein (CREB) and phosphorylated CREB | Q71142960 | ||
| Dynamic contributions to the DNA binding entropy of the EcoRI and EcoRV restriction endonucleases | Q71903639 | ||
| Structural and functional analysis of the NF-kappa B p65 C terminus. An acidic and modular transactivation domain with the potential to adopt an alpha-helical conformation | Q72724356 | ||
| Certain bZIP peptides bind DNA sequentially as monomers and dimerize on the DNA | Q73074187 | ||
| Long range interaction of cis-DNA elements mediated by architectural transcription factor Bach1 | Q73321794 | ||
| The role of helix formation in the folding of a fully alpha-helical coiled coil | Q73365490 | ||
| Preformed secondary structure drives the association reaction of GCN4-p1, a model coiled-coil system | Q73472065 | ||
| Energy landscape theory, funnels, specificity, and optimal criterion of biomolecular binding | Q73478247 | ||
| How transcriptional activators bind target proteins | Q74404396 | ||
| Diffusion-controlled DNA recognition by an unfolded, monomeric bZIP transcription factor | Q74440413 | ||
| Temperature dependence of intramolecular dynamics of the basic leucine zipper of GCN4: implications for the entropy of association with DNA | Q77928344 | ||
| Role of intrinsic disorder in transient interactions of hub proteins | Q79416219 | ||
| Activated signal transduction kinases frequently occupy target genes | Q80011658 | ||
| Exploring the mechanism of flexible biomolecular recognition with single molecule dynamics | Q80331900 | ||
| Prediction of unfolded segments in a protein sequence based on amino acid composition | Q81289447 | ||
| Repression and coactivation of CCAAT/enhancer-binding protein epsilon by sumoylation and protein inhibitor of activated STATx proteins | Q81300131 | ||
| Intrinsic unstructuredness and abundance of PEST motifs in eukaryotic proteomes | Q81507965 | ||
| Structurally distinct modes of recognition of the KIX domain of CBP by Jun and CREB. | Q55239673 | ||
| Structural Basis for Cooperative Transcription Factor Binding to the CBP Coactivator | Q57078210 | ||
| A shortcut to peptides to modulate platelets | Q57881034 | ||
| Latent and active p53 are identical in conformation | Q58002479 | ||
| DNA-induced increase in the .alpha.-helical content of C/EBP and GCN4 | Q58450838 | ||
| C/EBP proteins contain nuclear localization signals imbedded in their basic regions | Q58707964 | ||
| Folding transition in the DMA-binding domain of GCN4 on specific binding to DNA | Q59067060 | ||
| Acid blobs and negative noodles | Q59070926 | ||
| Negative effect of the transcriptional activator GAL4 | Q59072863 | ||
| Kinetic Studies of Fos·Jun·DNA Complex Formation: DNA Binding Prior to Dimerization† | Q62516312 | ||
| Sequence patterns associated with disordered regions in proteins | Q62660449 | ||
| Human transcription factors contain a high fraction of intrinsically disordered regions essential for transcriptional regulation | Q64111661 | ||
| Intrinsically disordered loops inserted into the structural domains of human proteins | Q64111735 | ||
| Intrinsically unstructured N-terminal domain of bZIP transcription factor HY5. | Q65000375 | ||
| Dimerization specificity of the leucine zipper-containing bZIP motif on DNA binding: prediction and rational design | Q70744379 | ||
| Predicting specificity in bZIP coiled-coil protein interactions | Q24807107 | ||
| Systematic discovery of new recognition peptides mediating protein interaction networks | Q24817114 | ||
| Solution structure of the transactivation domain of ATF-2 comprising a zinc finger-like subdomain and a flexible subdomain | Q27617761 | ||
| Structural basis of recognition of monopartite and bipartite nuclear localization sequences by mammalian importin-alpha | Q27622214 | ||
| The structure of a CREB bZIP.somatostatin CRE complex reveals the basis for selective dimerization and divalent cation-enhanced DNA binding | Q27626640 | ||
| Structural basis for the diversity of DNA recognition by bZIP transcription factors | Q27627308 | ||
| Crystal structure of the CCAAT box/enhancer-binding protein beta activating transcription factor-4 basic leucine zipper heterodimer in the absence of DNA | Q27627331 | ||
| Structures of HIV-1 gp120 envelope glycoproteins from laboratory-adapted and primary isolates | Q27629806 | ||
| Mechanism of c-Myb-C/EBP beta cooperation from separated sites on a promoter | Q27637335 | ||
| Solution structure of the DNA-binding domain of MafG | Q27638137 | ||
| Structural basis for DNA recognition by the basic region leucine zipper transcription factor CCAAT/enhancer-binding protein alpha | Q27640476 | ||
| The structure of importin-beta bound to SREBP-2: nuclear import of a transcription factor | Q27642661 | ||
| The GCN4 basic region leucine zipper binds DNA as a dimer of uninterrupted alpha helices: crystal structure of the protein-DNA complex | Q27642986 | ||
| Crystal structure of the heterodimeric bZIP transcription factor c-Fos-c-Jun bound to DNA | Q27730317 | ||
| Crystal structure of a p53 tumor suppressor-DNA complex: understanding tumorigenic mutations | Q27730815 | ||
| A switch between two-, three-, and four-stranded coiled coils in GCN4 leucine zipper mutants | Q27731470 | ||
| Solution Structure of the KIX Domain of CBP Bound to the Transactivation Domain of CREB: A Model for Activator:Coactivator Interactions | Q27748755 | ||
| Structure of the DNA-binding domains from NFAT, Fos and Jun bound specifically to DNA | Q27748936 | ||
| The Pfam protein families database | Q27860470 | ||
| The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins | Q27860587 | ||
| The atomic structure of protein-protein recognition sites | Q27861113 | ||
| CBP/p300 in cell growth, transformation, and development | Q28140313 | ||
| Comprehensive identification of human bZIP interactions with coiled-coil arrays | Q28178993 | ||
| CCAAT/enhancer-binding protein family members recruit the coactivator CREB-binding protein and trigger its phosphorylation | Q28186842 | ||
| Transcriptional coactivator complexes | Q28200751 | ||
| AP-1--Introductory remarks | Q28201502 | ||
| HMGI/Y proteins: flexible regulators of transcription and chromatin structure | Q28201754 | ||
| Enhanceosomes | Q28204862 | ||
| Extended disordered proteins: targeting function with less scaffold | Q28208096 | ||
| BRCT Repeats As Phosphopeptide-Binding Modules Involved in Protein Targeting | Q28212263 | ||
| Induced alpha helix in the VP16 activation domain upon binding to a human TAF | Q28247311 | ||
| Analysis of molecular recognition features (MoRFs) | Q28260253 | ||
| CREB is a regulatory target for the protein kinase Akt/PKB | Q28289946 | ||
| Roles of partly unfolded conformations in macromolecular self-assembly | Q34135691 | ||
| Recognition between flexible protein molecules: induced and assisted folding | Q34141716 | ||
| Site-specific thermodynamics and kinetics of a coiled-coil transition by spin inversion transfer NMR. | Q34168189 | ||
| C/EBP family transcription factors are degraded by the proteasome but stabilized by forming dimer | Q34181499 | ||
| The multiple nuclear functions of BRCA1: transcription, ubiquitination and DNA repair | Q34203060 | ||
| Nucleocytoplasmic transport enters the atomic age. | Q34245364 | ||
| Close encounters of many kinds: Fos-Jun interactions that mediate transcription regulatory specificity. | Q34279362 | ||
| CBP, a transcriptional coactivator and acetyltransferase | Q34316264 | ||
| DisProt: a database of protein disorder | Q34341031 | ||
| The mammalian Mediator complex and its role in transcriptional regulation | Q34419211 | ||
| FoldIndex: a simple tool to predict whether a given protein sequence is intrinsically unfolded | Q34426417 | ||
| The Maf transcription factors: regulators of differentiation | Q34449145 | ||
| Recognition of specific DNA sequences. | Q34462035 | ||
| Deciphering B-ZIP transcription factor interactions in vitro and in vivo | Q34507956 | ||
| One billion years of bZIP transcription factor evolution: conservation and change in dimerization and DNA-binding site specificity | Q34595874 | ||
| Simulating disorder-order transitions in molecular recognition of unstructured proteins: where folding meets binding | Q34982184 | ||
| Heat capacity and entropy changes in processes involving proteins | Q35063139 | ||
| Eukaryotic transcriptional regulatory complexes: cooperativity from near and afar | Q35064520 | ||
| Differential gene regulation by selective association of transcriptional coactivators and bZIP DNA-binding domains | Q35071079 | ||
| Speeding molecular recognition by using the folding funnel: the fly-casting mechanism | Q35189399 | ||
| NORSp: Predictions of long regions without regular secondary structure | Q35207504 | ||
| Dimerization specificity of all 67 B-ZIP motifs in Arabidopsis thaliana: a comparison to Homo sapiens B-ZIP motifs | Q35618162 | ||
| Energy transfer analysis of Fos-Jun dimerization and DNA binding | Q35631538 | ||
| Intrinsic disorder and functional proteomics | Q35632957 | ||
| DNA specificity enhanced by sequential binding of protein monomers. | Q35707608 | ||
| Optimal specificity and function for flexible biomolecular recognition | Q35812281 | ||
| Intrinsic disorder as a mechanism to optimize allosteric coupling in proteins | Q35850129 | ||
| Unfolded proteins and protein folding studied by NMR. | Q35860163 | ||
| Natively unfolded proteins | Q36046424 | ||
| Showing your ID: intrinsic disorder as an ID for recognition, regulation and cell signaling | Q36226283 | ||
| Can you hear me now? Regulating transcriptional activators by phosphorylation | Q36256383 | ||
| Assessing protein disorder and induced folding | Q36312787 | ||
| Structure of the leucine zipper | Q36354797 | ||
| Multisite and hierarchal protein phosphorylation. | Q36407163 | ||
| BRCA1-mediated ubiquitylation | Q36544363 | ||
| The role of helix stabilizing residues in GCN4 basic region folding and DNA binding | Q36639578 | ||
| Comparing function and structure between entire proteomes | Q36640722 | ||
| Posttranslational modifications and subcellular localization signals: indicators of sequence regions without inherent 3D structure? | Q36789780 | ||
| Conservation of intrinsic disorder in protein domains and families: II. functions of conserved disorder | Q36869604 | ||
| Intrinsic disorder in transcription factors | Q36882145 | ||
| The C/EBP family of transcription factors: a paradigm for interaction between gene expression and proliferation control | Q36893970 | ||
| Diversity and specificity in transcriptional regulation: the benefits of heterotypic dimerization | Q36924764 | ||
| Transmembrane bZIP transcription factors in ER stress signaling and the unfolded protein response | Q36948672 | ||
| A specific lysine in c-Jun is required for transcriptional repression by E1A and is acetylated by p300 | Q28363091 | ||
| Nuclear export of phosphorylated C/EBPbeta mediates the inhibition of albumin expression by TNF-alpha | Q28365498 | ||
| The importance of intrinsic disorder for protein phosphorylation | Q28776125 | ||
| Intrinsic structural disorder of the C-terminal activation domain from the bZIP transcription factor Fos | Q28910425 | ||
| Recent improvements to the SMART domain-based sequence annotation resource | Q29614230 | ||
| Evidence for dynamically organized modularity in the yeast protein-protein interaction network | Q29614449 | ||
| Cooperation between complexes that regulate chromatin structure and transcription | Q29614769 | ||
| Intrinsically unstructured proteins | Q29614784 | ||
| A unified theory of gene expression | Q29615022 | ||
| Transcriptional activation by recruitment | Q29615048 | ||
| GlobPlot: Exploring protein sequences for globularity and disorder | Q29615737 | ||
| Why are "natively unfolded" proteins unstructured under physiologic conditions? | Q29615739 | ||
| Intrinsically unstructured proteins: re-assessing the protein structure-function paradigm | Q29615865 | ||
| Intrinsic disorder and protein function | Q29616415 | ||
| Natively unfolded proteins: a point where biology waits for physics | Q29616416 | ||
| Coupling of folding and binding for unstructured proteins | Q29616417 | ||
| Sequence complexity of disordered protein | Q29616420 | ||
| Coupling of local folding to site-specific binding of proteins to DNA | Q29616464 | ||
| Integration and diversity of the regulatory network composed of Maf and CNC families of transcription factors | Q29616505 | ||
| Transcription regulation and animal diversity | Q29618752 | ||
| Comparing and combining predictors of mostly disordered proteins. | Q30350136 | ||
| The interplay between structure and function in intrinsically unstructured proteins. | Q30350853 | ||
| Flexible nets. The roles of intrinsic disorder in protein interaction networks. | Q30351593 | ||
| Predicting protein disorder and induced folding: from theoretical principles to practical applications. | Q30361055 | ||
| A thermodynamic scale for leucine zipper stability and dimerization specificity: e and g interhelical interactions | Q30420444 | ||
| Discovering high mobility group A molecular partners in tumour cells | Q30780691 | ||
| B-ZIP proteins encoded by the Drosophila genome: evaluation of potential dimerization partners | Q30842837 | ||
| Single-molecule dynamics reveals cooperative binding-folding in protein recognition | Q33250076 | ||
| Inferring function using patterns of native disorder in proteins | Q33295214 | ||
| Multiprotein-DNA complexes in transcriptional regulation | Q33689910 | ||
| Fundamentally different logic of gene regulation in eukaryotes and prokaryotes | Q33691046 | ||
| D-site binding protein transactivation requires the proline- and acid-rich domain and involves the coactivator p300. | Q33864495 | ||
| Deciphering genetic regulatory codes: a challenge for functional genomics | Q33893968 | ||
| Genome-wide analysis of cAMP-response element binding protein occupancy, phosphorylation, and target gene activation in human tissues | Q33934262 | ||
| Docking domains and substrate-specificity determination for MAP kinases | Q34023280 | ||
| Transcription factors 1: bZIP proteins. | Q34059000 | ||
| The molecular biology and nomenclature of the activating transcription factor/cAMP responsive element binding family of transcription factors: activating transcription factor proteins and homeostasis | Q34085639 | ||
| A transcriptional switch mediated by cofactor methylation | Q34101080 | ||
| Modular structure of transcription factors: implications for gene regulation | Q34110705 | ||
| Cell cycle-dependent phosphorylation of C/EBPbeta mediates oncogenic cooperativity between C/EBPbeta and H-RasV12. | Q37349767 | ||
| Degradation of nuclear oncoproteins by the ubiquitin system in vitro | Q37361143 | ||
| Kinetic profiles of p300 occupancy in vivo predict common features of promoter structure and coactivator recruitment | Q37415446 | ||
| Coactivator MBF1 preserves the redox-dependent AP-1 activity during oxidative stress in Drosophila | Q37513758 | ||
| Crystal structure of ATF-2/c-Jun and IRF-3 bound to the interferon-beta enhancer | Q37605234 | ||
| CRP2 (C/EBP beta) contains a bipartite regulatory domain that controls transcriptional activation, DNA binding and cell specificity | Q37619789 | ||
| Extending dimerization interfaces: the bZIP basic region can form a coiled coil. | Q37624408 | ||
| CCAAT/enhancer binding protein-alpha amino acid motifs with dual TBP and TFIIB binding ability co-operate to activate transcription in both yeast and mammalian cells | Q38292246 | ||
| Cell signaling. Protein kinases seek close encounters with active genes | Q38311110 | ||
| Dimerization of a specific DNA-binding protein on the DNA. | Q38331100 | ||
| bZIPDB: a database of regulatory information for human bZIP transcription factors | Q38516119 | ||
| Recruitment of p300 by C/EBPbeta triggers phosphorylation of p300 and modulates coactivator activity | Q39714611 | ||
| The interaction of C-Rel with C/EBPbeta enhances C/EBPbeta binding to the C-reactive protein gene promoter | Q40163728 | ||
| Coregulated ataxia telangiectasia-mutated and casein kinase sites modulate cAMP-response element-binding protein-coactivator interactions in response to DNA damage | Q40185672 | ||
| Phospho-dependent protein recognition motifs contained in C/EBP family of transcription factors: in silico studies. | Q40208829 | ||
| Mechanism of coupled folding and binding of an intrinsically disordered protein | Q40210194 | ||
| Regulation of the transcriptional activity of c-Fos by ERK. A novel role for the prolyl isomerase PIN1. | Q40381392 | ||
| Structure and function of transcriptional activation domains | Q40445589 | ||
| Phosphorylation of the c-Fos and c-Jun HOB1 motif stimulates its activation capacity | Q40523051 | ||
| Transcriptional regulation by extracellular signals: mechanisms and specificity | Q40579098 | ||
| Regulation of CCAAT/enhancer-binding protein (C/EBP) activator proteins by heterodimerization with C/EBPgamma (Ig/EBP). | Q40735316 | ||
| cAMP response element-binding protein monomers cooperatively assemble to form dimers on DNA. | Q41018786 | ||
| Identification of transcriptional activation and repression domains in human CCAAT/enhancer-binding protein epsilon | Q41034641 | ||
| The DNA binding domain of the rat liver nuclear protein C/EBP is bipartite | Q41260447 | ||
| Probing the partly folded states of proteins by limited proteolysis | Q41458691 | ||
| Win some, lose some: enthalpy-entropy compensation in weak intermolecular interactions | Q41651485 | ||
| The basic leucine zipper domain of c-Jun functions in transcriptional activation through interaction with the N terminus of human TATA-binding protein-associated factor-1 (human TAF(II)250). | Q42460323 | ||
| Transcriptional repression of peroxisome proliferator-activated receptor beta/delta in murine keratinocytes by CCAAT/enhancer-binding proteins | Q42484044 | ||
| CCAAT/enhancer-binding protein (C/EBP) beta is acetylated at multiple lysines: acetylation of C/EBPbeta at lysine 39 modulates its ability to activate transcription | Q42833598 | ||
| In vitro DNA binding activity of Fos/Jun and BZLF1 but not C/EBP is affected by redox changes | Q43503907 | ||
| Molecular shapes of transcription factors TFIIB and VP16 in solution: implications for recognition | Q43616285 | ||
| Unfolding of a leucine zipper is not a simple two-state transition | Q44121897 | ||
| Solution structure of the KIX domain of CBP bound to the transactivation domain of c-Myb | Q44799099 | ||
| Characterization of segments from the central region of BRCA1: an intrinsically disordered scaffold for multiple protein-protein and protein-DNA interactions? | Q45168174 | ||
| N and C-terminal sub-regions in the c-Myc transactivation region and their joint role in creating versatility in folding and binding | Q45233314 | ||
| Primary contact sites in intrinsically unstructured proteins: the case of calpastatin and microtubule-associated protein 2. | Q45307728 | ||
| Structural studies of the acidic transactivation domain of the Vmw65 protein of herpes simplex virus using 1H NMR | Q45879786 | ||
| Structure-based design of a dimeric zinc finger protein. | Q45885544 | ||
| Structure-based prediction of bZIP partnering specificity. | Q45966174 | ||
| A survey of flexible protein binding mechanisms and their transition states using native topology based energy landscapes | Q46212322 | ||
| Preformed structural elements feature in partner recognition by intrinsically unstructured proteins | Q47692263 | ||
| Flavors of protein disorder | Q47700031 | ||
| Accessory factor-bZIP-DNA interactions | Q47829676 | ||
| Identification of novel glycogen synthase kinase-3beta substrate-interacting residues suggests a common mechanism for substrate recognition | Q47843402 | ||
| Regulation of nuclear import by phosphorylation adjacent to nuclear localization signals | Q48004807 | ||
| Importins and exportins: how to get in and out of the nucleus | Q48014918 | ||
| Coupled folding and binding with alpha-helix-forming molecular recognition elements | Q48122045 | ||
| The protein trinity--linking function and disorder. | Q52055900 | ||
| Thermodynamic characterization of the structural stability of the coiled-coil region of the bZIP transcription factor GCN4. | Q52395143 | ||
| DNA binding and phosphorylation induce conformational alterations in the kinase-inducible domain of CREB. Implications for the mechanism of transcription function. | Q52679677 | ||
| Cell biology: brief encounters bolster contacts. | Q55042605 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 244-269 | |
| P577 | publication date | 2009-06-01 | |
| P1433 | published in | Current Protein and Peptide Science | Q15745198 |
| P1476 | title | The importance of being flexible: the case of basic region leucine zipper transcriptional regulators | |
| P478 | volume | 10 |
| Q33796245 | A multiprotein binding interface in an intrinsically disordered region of the tumor suppressor protein interferon regulatory factor-1 |
| Q90023588 | Analysis of NMR Spin-Relaxation Data Using an Inverse Gaussian Distribution Function |
| Q36389392 | Basic leucine zipper transcription factor Hac1 binds DNA in two distinct modes as revealed by microfluidic analyses |
| Q37699087 | Combinatorial bZIP dimers display complex DNA-binding specificity landscapes. |
| Q34500405 | Complex modulation of the Aedes aegypti transcriptome in response to dengue virus infection |
| Q41853245 | Conformational Dynamics of the Partially Disordered Yeast Transcription Factor GCN4 |
| Q30962241 | Conformational ensembles explored dynamically from disordered peptides targeting chemokine receptor CXCR4. |
| Q34682232 | Conserved structural domains in FoxD4L1, a neural forkhead box transcription factor, are required to repress or activate target genes |
| Q27332088 | Cryptocephal, the Drosophila melanogaster ATF4, is a specific coactivator for ecdysone receptor isoform B2 |
| Q34943653 | Cryptococcus neoformans Yap1 is required for normal fluconazole and oxidative stress resistance |
| Q41544212 | Deciphering the combinatorial DNA-binding code of the CCAAT-binding complex and the iron-regulatory basic region leucine zipper (bZIP) transcription factor HapX. |
| Q36971798 | Dynamics of GCN4 facilitate DNA interaction: a model-free analysis of an intrinsically disordered region |
| Q36137308 | ERK5 protein promotes, whereas MEK1 protein differentially regulates, the Toll-like receptor 2 protein-dependent activation of human endothelial cells and monocytes |
| Q34197530 | Expanding the proteome: disordered and alternatively folded proteins |
| Q51438298 | Exploring c-Met kinase flexibility by sampling and clustering its conformational space. |
| Q91706583 | Low-Affinity Binding Sites and the Transcription Factor Specificity Paradox in Eukaryotes |
| Q27011309 | Mechanisms of apoptosis by the tumor suppressor Par-4 |
| Q27008904 | Molecular mechanisms of prolactin and its receptor |
| Q59138244 | Nach Is a Novel Subgroup at an Early Evolutionary Stage of the CNC-bZIP Subfamily Transcription Factors from the Marine Bacteria to Humans |
| Q45053036 | Nuclear localization of a putative Phytophthora sojae bZIP1 transcription factor is mediated by multiple targeting motifs. |
| Q39183210 | OsbZIP71, a bZIP transcription factor, confers salinity and drought tolerance in rice |
| Q94503735 | Pathogenicity-associated protein domains: The fiercely-conserved evolutionary signatures |
| Q37863055 | Plant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network |
| Q34152667 | Polyglutamine repeats are associated to specific sequence biases that are conserved among eukaryotes. |
| Q93132974 | Polymer effects modulate binding affinities in disordered proteins |
| Q38725653 | Quantitative Analysis of the DNA Methylation Sensitivity of Transcription Factor Complexes |
| Q96432548 | Self-assembly of the bZIP transcription factor ΔFosB |
| Q35351996 | The N terminus of pro-endothelial monocyte-activating polypeptide II (EMAP II) regulates its binding with the C terminus, arginyl-tRNA synthetase, and neurofilament light protein |
| Q58780328 | The Unfolded Protein Response Pathway in the Yeast . A Comparative View among Yeast Species |
| Q35910684 | The diversification of the basic leucine zipper family in eukaryotes correlates with the evolution of multicellularity |
| Q39412639 | The effect of Zhangfei on the unfolded protein response and growth of cells derived from canine and human osteosarcomas. |
| Q50914408 | The intrinsically disordered C-terminal region of Arabidopsis thaliana TCP8 transcription factor acts both as a transactivation and self-assembly domain. |
| Q34961642 | Viral proteins originated de novo by overprinting can be identified by codon usage: application to the "gene nursery" of Deltaretroviruses |
| Q37263599 | bZIP transcription factors in the oomycete phytophthora infestans with novel DNA-binding domains are involved in defense against oxidative stress |
| Q38211021 | bZIPs and WRKYs: two large transcription factor families executing two different functional strategies |
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