scholarly article | Q13442814 |
P50 | author | Michelle D Leach | Q55743461 |
Alistair J P Brown | Q30502927 | ||
P2093 | author name string | A. J. P. Brown | |
M. D. Leach | |||
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Catabolite degradation of fructose-1,6-bisphosphatase in the yeast Saccharomyces cerevisiae: a genome-wide screen identifies eight novel GID genes and indicates the existence of two degradation pathways | Q27933074 | ||
Modification of yeast Cdc53p by the ubiquitin-related protein rub1p affects function of the SCFCdc4 complex | Q27933259 | ||
Ubc8p functions in catabolite degradation of fructose-1, 6-bisphosphatase in yeast | Q27933816 | ||
An essential function of Grr1 for the degradation of Cln2 is to act as a binding core that links Cln2 to Skp1. | Q27934791 | ||
Rtt109 acetylates histone H3 lysine 56 and functions in DNA replication | Q27935707 | ||
Pds5p regulates the maintenance of sister chromatid cohesion and is sumoylated to promote the dissolution of cohesion | Q27936246 | ||
The septins: roles in cytokinesis and other processes | Q27936270 | ||
Cell cycle-regulated attachment of the ubiquitin-related protein SUMO to the yeast septins | Q27936336 | ||
Cryptococcus neoformans mating and virulence are regulated by the G-protein α subunit GPA1 and cAMP | Q35197981 | ||
Increased ubiquitin-dependent degradation can replace the essential requirement for heat shock protein induction | Q35208828 | ||
Roles of Ras1 membrane localization during Candida albicans hyphal growth and farnesol response | Q35530373 | ||
Proteasomes and molecular chaperones: cellular machinery responsible for folding and destruction of unfolded proteins | Q35544930 | ||
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How to activate a damage-tolerant polymerase: consequences of PCNA modifications by ubiquitin and SUMO. | Q35601065 | ||
Role of protein O-mannosyltransferase Pmt4 in the morphogenesis and virulence of Cryptococcus neoformans | Q35636471 | ||
Regulation of apoptosis proteins in cancer cells by ubiquitin | Q35691538 | ||
On the mechanism of protein palmitoylation | Q35936412 | ||
Protein arginine methylation in Candida albicans: role in nuclear transport | Q35947027 | ||
Post-translational modifications influence transcription factor activity: a view from the ETS superfamily | Q36043735 | ||
Mitogen-activated protein kinase pathways and fungal pathogenesis | Q36095378 | ||
Septins may form a ubiquitous family of cytoskeletal filaments | Q36237412 | ||
Lingering mysteries of ubiquitin-chain assembly | Q36368593 | ||
Two-component signal transduction in human fungal pathogens | Q36399917 | ||
SUMO-targeted ubiquitin ligases in genome stability. | Q36439087 | ||
Ubiquitination | Q36467132 | ||
Co-ordinated covalent modification of G-protein coupled receptors | Q36483090 | ||
Comprehensive analysis of glycosylphosphatidylinositol-anchored proteins in Candida albicans | Q36692630 | ||
Regulation of histone H3 lysine 56 acetylation in Schizosaccharomyces pombe | Q43852300 | ||
The small ubiquitin-like modifier (SUMO) protein modification system in Arabidopsis. Accumulation of SUMO1 and -2 conjugates is increased by stress. | Q44249813 | ||
Multiple Functions of Pmt1p-mediated ProteinO-Mannosylation in the Fungal Pathogen Candida albicans | Q44822932 | ||
A tandem affinity tag for two-step purification under fully denaturing conditions: application in ubiquitin profiling and protein complex identification combined with in vivocross-linking | Q46181926 | ||
Disulfide bond structure and domain organization of yeast beta(1,3)-glucanosyltransferases involved in cell wall biogenesis. | Q46603180 | ||
The NED-8 conjugating system in Caenorhabditis elegans is required for embryogenesis and terminal differentiation of the hypodermis | Q47068910 | ||
Rad6p represses yeast-hypha morphogenesis in the human fungal pathogen Candida albicans | Q47878543 | ||
Molecular characterization of ubiquitin genes from Aspergillus nidulans: mRNA expression on different stress and growth conditions | Q47883191 | ||
Catalytic isoforms Tpk1 and Tpk2 of Candida albicans PKA have non-redundant roles in stress response and glycogen storage. | Q47949543 | ||
The Drosophila semushi mutation blocks nuclear import of bicoid during embryogenesis | Q48007223 | ||
A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae | Q48017973 | ||
Structure of the ubiquitin-encoding genes of cryptococcus neoformans | Q48071504 | ||
The Aspergillus nidulans F-box protein GrrA links SCF activity to meiosis. | Q48086255 | ||
Structure of a yeast pheromone gene (MF alpha): a putative alpha-factor precursor contains four tandem copies of mature alpha-factor | Q48402745 | ||
SUMO modification of septin-interacting proteins in Candida albicans | Q50797640 | ||
TheCandida albicans UBI3gene encoding a hybrid ubiquitin fusion protein involved in ribosome biogenesis is essential for growth | Q52550234 | ||
Outer chain N-glycans are required for cell wall integrity and virulence of Candida albicans | Q52566975 | ||
Members of protein O-mannosyltransferase family in Aspergillus fumigatus differentially affect growth, morphogenesis and viability | Q52599841 | ||
Granulocytes govern the transcriptional response, morphology and proliferation of Candida albicans in human blood | Q52939255 | ||
The F-box protein Grr1 regulates the stability of Ccn1, Cln3 and Hof1 and cell morphogenesis in Candida albicans | Q53598156 | ||
PMT family of Candida albicans: five protein mannosyltransferase isoforms affect growth, morphogenesis and antifungal resistance | Q53873705 | ||
Systematic study of protein sumoylation: Development of a site-specific predictor of SUMOsp 2.0 | Q56526462 | ||
Sequence differences between glycosylated and non-glycosylated Asn-X-Thr/Ser acceptor sites: implications for protein engineering | Q57381679 | ||
Molecular characterization of ubiquitin genes from Aspergillus nidulans: mRNA expression on different stress and growth conditions | Q60894858 | ||
Structure of Saccharomyces cerevisiae mating hormone a-factor. Identification of S-farnesyl cysteine as a structural component | Q70226827 | ||
Catabolite inactivation of fructose-1,6-bisphosphatase of Saccharomyces cerevisiae. Degradation occurs via the ubiquitin pathway | Q71823930 | ||
Catabolite inactivation of fructose-1,6-bisphosphatase in yeast is mediated by the proteasome | Q72107005 | ||
Depletion of polyubiquitin encoded by the UBI4 gene confers pleiotropic phenotype to Candida albicans cells | Q73383057 | ||
Ubiquitination and degradation of the substrate recognition subunits of SCF ubiquitin-protein ligases | Q77652490 | ||
Distinct and redundant roles of the two protein kinase A isoforms Tpk1p and Tpk2p in morphogenesis and growth of Candida albicans | Q77748392 | ||
Multistep disulfide bond formation in Yap1 is required for sensing and transduction of H2O2 stress signal | Q80813947 | ||
Folding and quality control of the VHL tumor suppressor proceed through distinct chaperone pathways | Q81813867 | ||
Genes involved in sister chromatid separation and segregation in the budding yeast Saccharomyces cerevisiae. | Q27936977 | ||
Nuclear-specific degradation of Far1 is controlled by the localization of the F-box protein Cdc4. | Q27937931 | ||
A novel protein modification pathway related to the ubiquitin system | Q27938072 | ||
Histone chaperone Asf1 is required for histone H3 lysine 56 acetylation, a modification associated with S phase in mitosis and meiosis | Q27938401 | ||
A new protease required for cell-cycle progression in yeast | Q27938681 | ||
Proteolytic activation of Rim1p, a positive regulator of yeast sporulation and invasive growth | Q27939291 | ||
The tails of ubiquitin precursors are ribosomal proteins whose fusion to ubiquitin facilitates ribosome biogenesis | Q27939801 | ||
Regulation of heat shock transcription factor 1 by stress-induced SUMO-1 modification | Q28116002 | ||
An E3-like factor that promotes SUMO conjugation to the yeast septins | Q28188846 | ||
Themes and variations on ubiquitylation | Q28206411 | ||
Multisite phosphorylation of a CDK inhibitor sets a threshold for the onset of DNA replication | Q28209282 | ||
SUMO: a history of modification | Q28243325 | ||
Protein disulfide isomerase | Q28263008 | ||
Palmitoylation of intracellular signaling proteins: regulation and function | Q28266189 | ||
Characterization of a Second Member of the Sentrin Family of Ubiquitin-like Proteins | Q28268631 | ||
All ras proteins are polyisoprenylated but only some are palmitoylated | Q28270312 | ||
Protein prenyltransferases | Q28277579 | ||
SUMO and ubiquitin in the nucleus: different functions, similar mechanisms? | Q28280175 | ||
SUMO-1 modification of IkappaBalpha inhibits NF-kappaB activation | Q28282094 | ||
Proteasome-independent functions of ubiquitin in endocytosis and signaling | Q28282959 | ||
The Set3/Hos2 histone deacetylase complex attenuates cAMP/PKA signaling to regulate morphogenesis and virulence of Candida albicans | Q28473928 | ||
Gene annotation and drug target discovery in Candida albicans with a tagged transposon mutant collection | Q28475711 | ||
Functional genomic analysis of C. elegans chromosome I by systematic RNA interference | Q29547812 | ||
Protein modification by SUMO | Q29547919 | ||
The diverse functions of histone lysine methylation | Q29614523 | ||
The yeast polyubiquitin gene is essential for resistance to high temperatures, starvation, and other stresses | Q29616169 | ||
Mechanisms of specificity in protein phosphorylation | Q29617541 | ||
Building ubiquitin chains: E2 enzymes at work | Q29619578 | ||
Morphogenesis in the yeast cell cycle: regulation by Cdc28 and cyclins | Q29620238 | ||
Multiple monoubiquitination of RTKs is sufficient for their endocytosis and degradation | Q29622825 | ||
Reading protein modifications with interaction domains | Q29622877 | ||
Identification of a multifunctional binding site on Ubc9p required for Smt3p conjugation | Q30857842 | ||
Molecular cloning and characterization of the Candida albicans UBI3 gene coding for a ubiquitin-hybrid protein | Q30952180 | ||
Cell cycle- and chaperone-mediated regulation of H3K56ac incorporation in yeast | Q33386002 | ||
GRR1 of Saccharomyces cerevisiae is required for glucose repression and encodes a protein with leucine-rich repeats | Q36736572 | ||
Chromatin challenges during DNA replication and repair | Q36744476 | ||
Thematic review series: lipid posttranslational modifications. GPI anchoring of protein in yeast and mammalian cells, or: how we learned to stop worrying and love glycophospholipids. | Q36759924 | ||
Inactivation of the phospholipase B gene PLB5 in wild-type Candida albicans reduces cell-associated phospholipase A2 activity and attenuates virulence | Q36787424 | ||
Methylation of proteins involved in translation | Q36870123 | ||
Function and regulation of protein neddylation. 'Protein modifications: beyond the usual suspects' review series | Q36946992 | ||
Lipid remodeling of GPI-anchored proteins and its function | Q36959266 | ||
Protein-O-mannosyltransferases in virulence and development | Q36988163 | ||
Stationary phase in the yeast Saccharomyces cerevisiae | Q37059288 | ||
Subcellular localization directs signaling specificity of the Cryptococcus neoformans Ras1 protein. | Q37099390 | ||
Remodeling of global transcription patterns of Cryptococcus neoformans genes mediated by the stress-activated HOG signaling pathways | Q37301922 | ||
Comparative genomics of MAP kinase and calcium-calcineurin signalling components in plant and human pathogenic fungi. | Q37537816 | ||
Tasting the fungal cell wall | Q37756214 | ||
Fine regulation of Saccharomyces cerevisiae MAPK pathways by post-translational modifications. | Q37773859 | ||
Sumoylation of Arabidopsis heat shock factor A2 (HsfA2) modifies its activity during acquired thermotholerance | Q38343560 | ||
Characterization of a fission yeast SUMO-1 homologue, pmt3p, required for multiple nuclear events, including the control of telomere length and chromosome segregation | Q39449792 | ||
HWP1 functions in the morphological development of Candida albicans downstream of EFG1, TUP1, and RBF1. | Q39497122 | ||
Morphogenesis, adhesive properties, and antifungal resistance depend on the Pmt6 protein mannosyltransferase in the fungal pathogen candida albicans | Q39499662 | ||
Survival defects of Cryptococcus neoformans mutants exposed to human cerebrospinal fluid result in attenuated virulence in an experimental model of meningitis | Q39669355 | ||
NEDD8 recruits E2-ubiquitin to SCF E3 ligase. | Q39731260 | ||
Proteinases, proteolysis and biological control in the yeast Saccharomyces cerevisiae | Q39845149 | ||
Grr1-dependent inactivation of Mth1 mediates glucose-induced dissociation of Rgt1 from HXT gene promoters | Q39855161 | ||
Identification and characterization of a Candida albicans mating pheromone | Q40172519 | ||
Covalent modifier NEDD8 is essential for SCF ubiquitin-ligase in fission yeast | Q40430046 | ||
Ubc9 is essential for viability of higher eukaryotic cells | Q40692747 | ||
The role of heat-shock proteins in thermotolerance | Q40709983 | ||
Acetylation of MyoD directed by PCAF is necessary for the execution of the muscle program | Q40908837 | ||
The PMT gene family: protein O-glycosylation in Saccharomyces cerevisiae is vital | Q41077782 | ||
The DOA pathway: studies on the functions and mechanisms of ubiquitin-dependent protein degradation in the yeast Saccharomyces cerevisiae | Q41125176 | ||
Acetylation of general transcription factors by histone acetyltransferases | Q41586010 | ||
Identification of sumoylation targets, combined with inactivation of SMT3, reveals the impact of sumoylation upon growth, morphology, and stress resistance in the pathogen Candida albicans. | Q41864652 | ||
Conserved function of RNF4 family proteins in eukaryotes: targeting a ubiquitin ligase to SUMOylated proteins | Q41943542 | ||
Global roles of Ssn6 in Tup1- and Nrg1-dependent gene regulation in the fungal pathogen, Candida albicans | Q42074010 | ||
Role of the heat shock transcription factor, Hsf1, in a major fungal pathogen that is obligately associated with warm-blooded animals. | Q42144146 | ||
Global analysis of protein sumoylation in Saccharomyces cerevisiae | Q42466529 | ||
Polyubiquitin gene expression contributes to oxidative stress resistance in respiratory yeast (Saccharomyces cerevisiae). | Q42501196 | ||
Saccharomyces cerevisiae ubiquitin-like protein Rub1 conjugates to cullin proteins Rtt101 and Cul3 in vivo. | Q42609853 | ||
Glucose promotes stress resistance in the fungal pathogen Candida albicans. | Q42636549 | ||
Defining the SUMO-modified proteome by multiple approaches in Saccharomyces cerevisiae | Q42642323 | ||
In silicio identification of glycosyl-phosphatidylinositol-anchored plasma-membrane and cell wall proteins of Saccharomyces cerevisiae | Q42670968 | ||
Histone H3-K56 acetylation is catalyzed by histone chaperone-dependent complexes | Q42850451 | ||
Global analyses of sumoylated proteins in Saccharomyces cerevisiae. Induction of protein sumoylation by cellular stresses | Q42931443 | ||
The Hsp70 chaperone Ssa1 is essential for catabolite induced degradation of the gluconeogenic enzyme fructose-1,6-bisphosphatase | Q43049904 | ||
Integration of transcriptional and posttranslational regulation in a glucose signal transduction pathway in Saccharomyces cerevisiae | Q43196958 | ||
Characterization of the PMT gene family in Cryptococcus neoformans | Q33487159 | ||
Candida albicans RIM101 pH response pathway is required for host-pathogen interactions | Q33592905 | ||
Ras signaling is required for serum-induced hyphal differentiation in Candida albicans. | Q33637947 | ||
How the cyclin became a cyclin: regulated proteolysis in the cell cycle | Q33641413 | ||
Histone acetyltransferase Rtt109 is required for Candida albicans pathogenesis. | Q33667782 | ||
Regulation of DNA-dependent activities by the functional motifs of the high-mobility-group chromosomal proteins | Q33689010 | ||
Regulatory networks controlling Candida albicans morphogenesis | Q33702252 | ||
Septins: cytoskeletal polymers or signalling GTPases? | Q33730378 | ||
A multifunctional mannosyltransferase family in Candida albicans determines cell wall mannan structure and host-fungus interactions. | Q33782528 | ||
Functional specialization and differential regulation of short-chain carboxylic acid transporters in the pathogen Candida albicans | Q33808815 | ||
Proteolysis and the cell cycle: with this RING I do thee destroy | Q33840470 | ||
Role for the SCFCDC4 ubiquitin ligase in Candida albicans morphogenesis | Q33841398 | ||
Recent advances in the study of prenylated proteins | Q33889074 | ||
Septin function in Candida albicans morphogenesis. | Q33902950 | ||
Ubiquitin-mediated proteolysis: biological regulation via destruction | Q33910576 | ||
The regulation of protein function by multisite phosphorylation--a 25 year update | Q33928103 | ||
Virulence of the fungal pathogen Candida albicans requires the five isoforms of protein mannosyltransferases | Q33946702 | ||
The histone deacetylase genes HDA1 and RPD3 play distinct roles in regulation of high-frequency phenotypic switching in Candida albicans | Q33996677 | ||
Nalpha -terminal acetylation of eukaryotic proteins | Q34050317 | ||
Cryptococcus neoformans histone acetyltransferase Gcn5 regulates fungal adaptation to the host | Q34055174 | ||
Regulation of gene expression by transcription factor acetylation | Q34058501 | ||
The Ulp1 SUMO isopeptidase: distinct domains required for viability, nuclear envelope localization, and substrate specificity | Q34185745 | ||
Histone acetylation and deacetylation in yeast | Q34187792 | ||
The ALS gene family of Candida albicans | Q34207790 | ||
Transferable domain in the G(1) cyclin Cln2 sufficient to switch degradation of Sic1 from the E3 ubiquitin ligase SCF(Cdc4) to SCF(Grr1). | Q34282128 | ||
Ubiquitin enters the new millennium | Q34388963 | ||
A role for cell-cycle-regulated histone H3 lysine 56 acetylation in the DNA damage response. | Q34433751 | ||
Sumoylation in Aspergillus nidulans: sumO inactivation, overexpression and live-cell imaging | Q34454789 | ||
Molecular organization of the cell wall of Candida albicans | Q34500159 | ||
Activation of the heat shock transcription factor Hsf1 is essential for the full virulence of the fungal pathogen Candida albicans | Q34544362 | ||
Molecular and proteomic analyses highlight the importance of ubiquitination for the stress resistance, metabolic adaptation, morphogenetic regulation and virulence of Candida albicans | Q34886777 | ||
Protein O-mannosylation: conserved from bacteria to humans | Q34980261 | ||
Proteolysis and the cell cycle | Q34995618 | ||
The F-Box Protein Fbp1 Regulates Sexual Reproduction and Virulence in Cryptococcus neoformans | Q35080879 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | SCF E3 ubiquitin ligase complex F-box protein grrA | Q62652120 |
P304 | page(s) | 98-108 | |
P577 | publication date | 2011-12-09 | |
P1433 | published in | Eukaryotic Cell | Q5408685 |
P1476 | title | Posttranslational modifications of proteins in the pathobiology of medically relevant fungi | |
P478 | volume | 11 |
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