| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1006988931 |
| P356 | DOI | 10.1038/NCB1121 |
| P3181 | OpenCitations bibliographic resource ID | 3918128 |
| P698 | PubMed publication ID | 15077114 |
| P50 | author | Subba Rao Setty | Q49611568 |
| Christopher G Burd | Q37393349 | ||
| P2093 | author name string | Charles Boone | |
| Amy Hin Yan Tong | |||
| Todd I Strochlic | |||
| P2860 | cites work | N-Terminal modifications of the 19S regulatory particle subunits of the yeast proteasome | Q44264499 |
| Cytoplasmic N-terminal protein acetylation is required for efficient photosynthesis in Arabidopsis | Q48234144 | ||
| Structural Basis for Activation of ARF GTPase | Q56288670 | ||
| Mutational analysis of Saccharomyces cerevisiae ARF1 | Q72391791 | ||
| N-terminal hydrophobic residues of the G-protein ADP-ribosylation factor-1 insert into membrane phospholipids upon GDP to GTP exchange | Q73244046 | ||
| PCR-based engineering of yeast genome | Q74321438 | ||
| CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 | ||
| Structural basis for Arl1-dependent targeting of homodimeric GRIP domains to the Golgi apparatus | Q24298505 | ||
| Structural snapshots of the mechanism and inhibition of a guanine nucleotide exchange factor | Q24301031 | ||
| Recruitment to Golgi membranes of ADP-ribosylation factor 1 is mediated by the cytoplasmic domain of p23 | Q24534604 | ||
| Interaction of Arl1-GTP with GRIP domains recruits autoantigens Golgin-97 and Golgin-245/p230 onto the Golgi | Q24669600 | ||
| Global analysis of protein localization in budding yeast | Q27653962 | ||
| Ric1p and the Ypt6p GTPase function in a common pathway required for localization of trans-Golgi network membrane proteins | Q27931624 | ||
| N-terminal acetyltransferases and sequence requirements for N-terminal acetylation of eukaryotic proteins | Q27932762 | ||
| The ARF-like GTPases Arl1p and Arl3p act in a pathway that interacts with vesicle-tethering factors at the Golgi apparatus. | Q27933615 | ||
| FYVE domain targets Pib1p ubiquitin ligase to endosome and vacuolar membranes. | Q27933871 | ||
| An acidic sequence of a putative yeast Golgi membrane protein binds COPII and facilitates ER export | Q27934064 | ||
| Global mapping of the yeast genetic interaction network | Q27934987 | ||
| Golgi recruitment of GRIP domain proteins by Arf-like GTPase 1 is regulated by Arf-like GTPase 3. | Q27936914 | ||
| NatC Nalpha-terminal acetyltransferase of yeast contains three subunits, Mak3p, Mak10p, and Mak31p | Q27938862 | ||
| Mdm20 protein functions with Nat3 protein to acetylate Tpm1 protein and regulate tropomyosin-actin interactions in budding yeast | Q27938958 | ||
| Systematic genetic analysis with ordered arrays of yeast deletion mutants | Q28131618 | ||
| A novel Rab6-interacting domain defines a family of Golgi-targeted coiled-coil proteins | Q28141920 | ||
| Arf and its many interactors | Q28191279 | ||
| Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q29546523 | ||
| Iterated profile searches with PSI-BLAST--a tool for discovery in protein databases | Q29618634 | ||
| The GRIP domain - a novel Golgi-targeting domain found in several coiled-coil proteins | Q33859182 | ||
| A novel Golgi-localisation domain shared by a class of coiled-coil peripheral membrane proteins | Q33859187 | ||
| Two putative acetyltransferases, san and deco, are required for establishing sister chromatid cohesion in Drosophila | Q34280735 | ||
| A yeast t-SNARE involved in endocytosis | Q36914877 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | membrane protein | Q423042 |
| Arf family GTPase ARL3 YPL051W | Q27548228 | ||
| Peptide alpha-N-acetyltransferase MAK3 YPR051W | Q27548374 | ||
| Sys1p YJL004C | Q27552669 | ||
| P304 | page(s) | 414-9 | |
| P577 | publication date | 2004-05-01 | |
| P1433 | published in | Nature Cell Biology | Q1574111 |
| P1476 | title | Golgi targeting of ARF-like GTPase Arl3p requires its Nalpha-acetylation and the integral membrane protein Sys1p | |
| P478 | volume | 6 |
| Q57372787 | A Proteomic Analysis of Lysosomal Integral Membrane Proteins Reveals the Diverse Composition of the Organelle |
| Q38734296 | A Role for Human N-alpha Acetyltransferase 30 (Naa30) in Maintaining Mitochondrial Integrity |
| Q35935178 | A genetic interaction map of cell cycle regulators |
| Q92590541 | A novel NAA10 p.(R83H) variant with impaired acetyltransferase activity identified in two boys with ID and microcephaly |
| Q88634117 | A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy |
| Q27931694 | A yeast phenomic model for the gene interaction network modulating CFTR-ΔF508 protein biogenesis. |
| Q46234549 | ADP-ribosylation factor-like GTPase ARFRP1 is required for trans-Golgi to plasma membrane trafficking of E-cadherin. |
| Q90423666 | ARFRP1 functions upstream of ARL1 and ARL5 to coordinate recruitment of distinct tethering factors to the trans-Golgi network |
| Q50299821 | ARFRP1 recruits ARL1 to the TGN |
| Q63342587 | ARL1 Plays a Role in the Binding of the GRIP Domain of a Peripheral Matrix Protein to the Golgi Apparatus in Plant Cells |
| Q36565138 | Absence of N-terminal acetyltransferase diversification during evolution of eukaryotic organisms |
| Q90801937 | Actin's N-terminal acetyltransferase uncovered |
| Q34502171 | An N-terminally acetylated Arf-like GTPase is localised to lysosomes and affects their motility |
| Q27934287 | Arl1p regulates spatial membrane organization at the trans-Golgi network through interaction with Arf-GEF Gea2p and flippase Drs2p. |
| Q42408800 | Autoregulation of Sec7 Arf-GEF activity and localization by positive feedback |
| Q28253618 | Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects |
| Q90669731 | Biochemical and structural analysis of N-terminal acetyltransferases |
| Q92410379 | Co-translational, Post-translational, and Non-catalytic Roles of N-Terminal Acetyltransferases |
| Q90580316 | Control of protein degradation by N-terminal acetylation and the N-end rule pathway |
| Q28596558 | Crystal Structure of the Golgi-Associated Human Nα-Acetyltransferase 60 Reveals the Molecular Determinants for Substrate-Specific Acetylation |
| Q24315920 | Crystal structure of the ARL2-GTP-BART complex reveals a novel recognition and binding mode of small GTPase with effector |
| Q42078648 | Depletion of the human N-terminal acetyltransferase hNaa30 disrupts Golgi integrity and ARFRP1 localization |
| Q38446887 | Developmental roles of protein N-terminal acetylation |
| Q24312046 | Differential effects of depletion of ARL1 and ARFRP1 on membrane trafficking between the trans-Golgi network and endosomes |
| Q101165952 | Divergent architecture of the heterotrimeric NatC complex explains N-terminal acetylation of cognate substrates |
| Q42784055 | Dysregulated Arl1, a regulator of post-Golgi vesicle tethering, can inhibit endosomal transport and cell proliferation in yeast |
| Q41977426 | Effect of the N-Terminal Helix and Nucleotide Loading on the Membrane and Effector Binding of Arl2/3. |
| Q37375715 | Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency |
| Q37202249 | Exploring the conservation of synthetic lethal genetic interaction networks |
| Q26738713 | First Things First: Vital Protein Marks by N-Terminal Acetyltransferases |
| Q27935424 | Genome-wide screen for inner nuclear membrane protein targeting in Saccharomyces cerevisiae: roles for N-acetylation and an integral membrane protein |
| Q27936769 | Global analysis of yeast endosomal transport identifies the vps55/68 sorting complex |
| Q55470095 | Investigating the functionality of a ribosome-binding mutant of NAA15 using Saccharomyces cerevisiae. |
| Q38772657 | Invited review: Small GTPases and their GAPs |
| Q24319663 | Knockdown of human N alpha-terminal acetyltransferase complex C leads to p53-dependent apoptosis and aberrant human Arl8b localization |
| Q34584756 | Knockout of Arfrp1 leads to disruption of ARF-like1 (ARL1) targeting to the trans-Golgi in mouse embryos and HeLa cells |
| Q37869708 | Mechanisms of protein retention in the Golgi |
| Q41333839 | Microscopy-based Saccharomyces cerevisiae complementation model reveals functional conservation and redundancy of N-terminal acetyltransferases |
| Q98948614 | Molecular basis for N-terminal alpha-synuclein acetylation by human NatB |
| Q50207923 | Molecular determinants of the N-terminal acetyltransferase Naa60 anchoring to the Golgi membrane. |
| Q41770482 | Mutation of an Arabidopsis NatB N-alpha-terminal acetylation complex component causes pleiotropic developmental defects |
| Q27674398 | N-Terminal Acetylation Acts as an Avidity Enhancer Within an Interconnected Multiprotein Complex |
| Q26765414 | N-Terminal Acetylation-Targeted N-End Rule Proteolytic System: The Ac/N-End Rule Pathway |
| Q60172513 | N-terminal Acetylation Levels Are Maintained During Acetyl-CoA Deficiency in |
| Q27935466 | N-terminal acetylation by NatC is not a general determinant for substrate subcellular localization in Saccharomyces cerevisiae |
| Q37461454 | N-terminal acetylation promotes synaptonemal complex assembly in C. elegans |
| Q90089526 | N-terminal acetylation stabilizes SIGMA FACTOR BINDING PROTEIN 1 involved in salicylic acid-primed cell death |
| Q47662340 | N-terminal acetylation targets GTPases to membranes. |
| Q27011436 | N-terminal modifications of cellular proteins: The enzymes involved, their substrate specificities and biological effects |
| Q36237829 | NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment |
| Q64961330 | NAA10-related syndrome. |
| Q30832532 | Naa50/San-dependent N-terminal acetylation of Scc1 is potentially important for sister chromatid cohesion |
| Q50299820 | NatC acetylates ARFFRP1 |
| Q21144944 | NatF contributes to an evolutionary shift in protein N-terminal acetylation and is important for normal chromosome segregation |
| Q36845704 | New insights into membrane trafficking and protein sorting. |
| Q36117175 | Nomenclature for the human Arf family of GTP-binding proteins: ARF, ARL, and SAR proteins |
| Q36327799 | Organelle identity and the signposts for membrane traffic |
| Q27935070 | Phospholipid transfer protein Sec14 is required for trafficking from endosomes and regulates distinct trans-Golgi export pathways. |
| Q34492928 | Physiological importance and identification of novel targets for the N-terminal acetyltransferase NatB. |
| Q42706640 | Probing the interaction between NatA and the ribosome for co-translational protein acetylation. |
| Q33491259 | Protein N-terminal acetylation: NAT 2007-2008 Symposia |
| Q34258775 | Protein N-terminal acetyltransferases in cancer |
| Q37898754 | Protein alpha-N-acetylation studied by N-terminomics |
| Q37864676 | Rabs and other small GTPases in ciliary transport |
| Q29617826 | Retrograde transport from endosomes to the trans-Golgi network |
| Q50299818 | SYS1 binds AcM-ARFRP1 |
| Q91753611 | Spatiotemporal dissection of the trans-Golgi network in budding yeast |
| Q90580496 | Spotlight on protein N-terminal acetylation |
| Q27675332 | Structural Conservation of Distinctive N-terminal Acetylation-Dependent Interactions across a Family of Mammalian NEDD8 Ligation Enzymes |
| Q55071574 | Synthetic lethal screen of NAA20, a catalytic subunit gene of NatB N-terminal acetylase in Saccharomyces cerevisiae. |
| Q27934182 | The GTPase Arf1p and the ER to Golgi cargo receptor Erv14p cooperate to recruit the golgin Rud3p to the cis-Golgi |
| Q34189152 | The N-end rule pathway and regulation by proteolysis |
| Q37705367 | The N-terminal methionine of cellular proteins as a degradation signal |
| Q28303621 | The NatA acetyltransferase couples Sup35 prion complexes to the [PSI+] phenotype |
| Q38604708 | The Sec7 N-terminal regulatory domains facilitate membrane-proximal activation of the Arf1 GTPase |
| Q28638824 | The biological functions of Naa10 - From amino-terminal acetylation to human disease |
| Q21560927 | The human N-alpha-acetyltransferase 40 (hNaa40p/hNatD) is conserved from yeast and N-terminally acetylates histones H2A and H4 |
| Q33320526 | The leishmania ARL-1 and Golgi traffic |
| Q28000022 | The small GTPases ARL-13 and ARL-3 coordinate intraflagellar transport and ciliogenesis |
| Q26746231 | The world of protein acetylation |
| Q27930772 | The yeast orthologue of GRASP65 forms a complex with a coiled-coil protein that contributes to ER to Golgi traffic |
| Q39868121 | Tool box: Plasmids for the expression or knockdown of human ARF Family GTPases (ARF/ARL/SAR) and their co-expression in bacteria with N-myristoyltransferases |
| Q33927359 | Towards a functional understanding of protein N-terminal acetylation |
| Q52321051 | Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. |
| Q27931950 | Two novel WD40 domain-containing proteins, Ere1 and Ere2, function in the retromer-mediated endosomal recycling pathway. |
| Q27936554 | Unfolded protein response regulates yeast small GTPase Arl1p activation at late Golgi via phosphorylation of Arf GEF Syt1p |
| Q34406735 | Vesicle trafficking maintains nuclear shape in Saccharomyces cerevisiae during membrane proliferation |
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