Multipurpose vectors designed for the fast generation of N- or C-terminal epitope-tagged proteins.
about
Induction of sporulation in Saccharomyces cerevisiae leads to the formation of N6-methyladenosine in mRNA: a potential mechanism for the activity of the IME4 gene.Maf1p, a negative effector of RNA polymerase III in Saccharomyces cerevisiaeAnatomy of a proficient enzyme: The structure of orotidine 5'-monophosphate decarboxylase in the presence and absence of a potential transition state analogThe ARG11 gene of Saccharomyces cerevisiae encodes a mitochondrial integral membrane protein required for arginine biosynthesis.Yeast Vps55p, a functional homolog of human obesity receptor gene-related protein, is involved in late endosome to vacuole trafficking.CNS1 encodes an essential p60/Sti1 homolog in Saccharomyces cerevisiae that suppresses cyclophilin 40 mutations and interacts with Hsp90.STT4 is an essential phosphatidylinositol 4-kinase that is a target of wortmannin in Saccharomyces cerevisiae.Recruitment of the yeast MADS-box proteins, ArgRI and Mcm1 by the pleiotropic factor ArgRIII is required for their stability.Gpi19, the Saccharomyces cerevisiae homologue of mammalian PIG-P, is a subunit of the initial enzyme for glycosylphosphatidylinositol anchor biosynthesis.ArgRII, a component of the ArgR-Mcm1 complex involved in the control of arginine metabolism in Saccharomyces cerevisiae, is the sensor of arginine.A dual role for zinc fingers in both DNA binding and zinc sensing by the Zap1 transcriptional activator.Role of Saccharomyces cerevisiae ISA1 and ISA2 in iron homeostasisDisruption of YHC8, a member of the TSR1 gene family, reveals its direct involvement in yeast protein translocation.Functional interactions between Hsp90 and the co-chaperones Cns1 and Cpr7 in Saccharomyces cerevisiae.Functions of FKBP12 and mitochondrial cyclophilin active site residues in vitro and in vivo in Saccharomyces cerevisiaeA novel Ras inhibitor, Eri1, engages yeast Ras at the endoplasmic reticulum.Specific copper transfer from the Cox17 metallochaperone to both Sco1 and Cox11 in the assembly of yeast cytochrome C oxidase.Functional analysis of Rrp7p, an essential yeast protein involved in pre-rRNA processing and ribosome assembly.Yeast epiarginase regulation, an enzyme-enzyme activity control: identification of residues of ornithine carbamoyltransferase and arginase responsible for enzyme catalytic and regulatory activities.Screening for toxic amyloid in yeast exemplifies the role of alternative pathway responsible for cytotoxicityCloning and characterization of CAD1/AAF1, a gene from Candida albicans that induces adherence to endothelial cells after expression in Saccharomyces cerevisiae.Independent metalloregulation of Ace1 and Mac1 in Saccharomyces cerevisiaeThe [URE3] prion is not conserved among Saccharomyces speciesThe toxicity of an "artificial" amyloid is related to how it interacts with membranes.Similarities between the DNA replication initiators of Gram-negative bacteria plasmids (RepA) and eukaryotes (Orc4p)/archaea (Cdc6p)Split-ubiquitin two-hybrid assay to analyze protein-protein interactions at the endosome: application to Saccharomyces cerevisiae Bro1 interacting with ESCRT complexes, the Doa4 ubiquitin hydrolase, and the Rsp5 ubiquitin ligase.PCF11 encodes a third protein component of yeast cleavage and polyadenylation factor I.Transcriptional regulation of the Zrg17 zinc transporter of the yeast secretory pathway.The cellular concentration of the yeast Ure2p prion protein affects its propagation as a prionEngineered bacterial hydrophobic oligopeptide repeats in a synthetic yeast prion, [REP-PSI (+)].Conservation of the prion properties of Ure2p through evolution.The mechanisms of [URE3] prion elimination demonstrate that large aggregates of Ure2p are dead-end products.A yeast model for amyloid-β aggregation exemplifies the role of membrane trafficking and PICALM in cytotoxicity.A structure-toxicity study of Aß42 reveals a new anti-parallel aggregation pathway.A subcomplex of RNA polymerase III subunits involved in transcription termination and reinitiation.Probing the role of oligomerization in the high thermal stability of Pyrococcus furiosus ornithine carbamoyltransferase by site-specific mutants.Binding to Elongin C inhibits degradation of interacting proteins in yeast.Metabolic channeling of carbamoyl phosphate, a thermolabile intermediate: evidence for physical interaction between carbamate kinase-like carbamoyl-phosphate synthetase and ornithine carbamoyltransferase from the hyperthermophile Pyrococcus furiosusPrediction of the functional effect of novel SLC25A13 variants using a S. cerevisiae model of AGC2 deficiency.
P2860
Q24537653-DAB5064C-3854-47AE-8AA1-F015D27652F4Q24550904-E53288C2-26FE-4910-8FB8-E8E8FBB1C66EQ27621462-B49C8299-2ABC-49A5-BCE9-CA8AADCA9C29Q27930085-19595B71-CB85-4E45-8DA7-9D88E74CEFE4Q27930454-27099DC6-B189-4D22-AB2D-6B084E2D9E03Q27930607-0D627B63-15E6-4215-B01B-AD9D552DC318Q27930696-7386F807-8093-4A6A-B126-4F77252939D5Q27931186-D69D8B2C-FC7E-454A-B6A9-B0AC97D2755EQ27931466-530C8D4C-45F7-4569-B9CF-6FF6F15080E9Q27932184-C26FC814-DAB4-40D8-BD6D-27F63903F311Q27932889-F4C478B1-6CA4-41A2-A2F3-6E87053114C7Q27932926-3E229695-BB54-4D7B-8250-673D57E703DEQ27933441-A2F90030-083E-4CB4-AD9F-378D45675F0CQ27933447-5DA6EDBA-1C83-4166-A491-0B627599825FQ27933868-B4A04CC5-1CDF-42A7-9A6D-3E2C5790B3A6Q27935341-F27B6EB6-B944-4D65-B921-FC9CBCAF82BFQ27935825-61AE4C30-A359-4AF0-B3E4-13828E950E22Q27937825-2B443450-9236-416D-B7F3-391BD7E94588Q27940294-91695F78-50B2-4460-8F90-B7C06BC75A96Q28474953-2F69F39C-ABB8-4C74-A133-B8257BB8A0FAQ32065058-CEC32C6B-27A4-435C-82C1-36E1691CA044Q34144006-CC967BFE-6070-4A84-94D3-299CC61CEABCQ34589020-6FFD9E88-C869-42CE-9062-A2593CBF5062Q35714133-64CA712D-EF04-42B3-A3FD-7B1E733A0EDAQ35857244-45E928C7-5E20-4BBC-889E-FFCB4C7F3FA0Q35947104-1588A921-84B3-49C6-A393-F554972C1213Q36565604-4125EC3B-70C8-479D-9643-DE47938FB5EEQ36719745-54B801D6-01B3-4657-B9F2-D5DA6770285EQ37158419-ED5863BB-BCAB-455F-A5A7-2B20825723D4Q39835239-B80DC348-E85C-454C-AD16-83D7E473BC8CQ39855212-1D9ADFC1-D019-4C6A-BDF9-00C4D8382079Q39927783-BC43FEFB-6BCF-4235-BAC9-AD1634264A47Q42260219-5A0FE2D3-16A5-41CA-8017-60E95FDFFB2EQ42913360-41FD1BDF-7216-4716-BE91-389703CEF842Q43192587-E351078D-FFB2-412D-A2BD-9626C1170D6DQ43674564-B1C7FBBE-4001-4F31-B517-611A914CF37CQ43895788-D6D17449-5250-406D-95DA-62A25159FC5CQ43917506-86C7E040-BFF6-4C26-A75F-443021508973Q52630605-5DEF30D0-F211-49F4-AD2A-AFA746FD7796
P2860
Multipurpose vectors designed for the fast generation of N- or C-terminal epitope-tagged proteins.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@en
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@nl
type
label
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@en
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@nl
prefLabel
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@en
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@nl
P2860
P356
P1433
P1476
Multipurpose vectors designed ...... minal epitope-tagged proteins.
@en
P2093
Minvielle-Sebastia L
P2860
P304
P356
10.1002/YEA.320100110
P577
1994-01-01T00:00:00Z