| scholarly article | Q13442814 |
| P356 | DOI | 10.1091/MBC.9.1.1 |
| P953 | full work available online at | https://europepmc.org/articles/PMC25209 |
| https://europepmc.org/articles/pmc25209?pdf=render | ||
| https://europepmc.org/articles/PMC25209?pdf=render | ||
| P932 | PMC publication ID | 25209 |
| P698 | PubMed publication ID | 9436987 |
| P5875 | ResearchGate publication ID | 13793519 |
| P2093 | author name string | C. S. Fishburn | |
| H. R. Bourne | |||
| J. Morales | |||
| P. T. Wilson | |||
| P2860 | cites work | BioTechniques | Q4914664 |
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| The 2.0 A crystal structure of a heterotrimeric G protein | Q27732250 | ||
| The G beta gamma complex of the yeast pheromone response pathway. Subcellular fractionation and protein-protein interactions | Q27934622 | ||
| Palmitoylation is required for signaling functions and membrane attachment of Gq alpha and Gs alpha | Q28255860 | ||
| Myristylation and palmitylation of Src family members: the fats of the matter | Q28259697 | ||
| All ras proteins are polyisoprenylated but only some are palmitoylated | Q28270312 | ||
| Arf proteins: the membrane traffic police? | Q28302542 | ||
| Targeting of nitric oxide synthase to endothelial cell caveolae via palmitoylation: implications for nitric oxide signaling | Q28609890 | ||
| Purification and properties of a palmitoyl-protein thioesterase that cleaves palmitate from H-Ras | Q28626381 | ||
| Inhibition of adenylyl cyclase by Gi alpha | Q28646204 | ||
| The myristoyl-electrostatic switch: a modulator of reversible protein-membrane interactions | Q29010955 | ||
| Protein lipidation in cell signaling | Q34308460 | ||
| Heterotrimeric G proteins: organizers of transmembrane signals | Q34317073 | ||
| Differential effects on cAMP on the MAP kinase cascade: evidence for a cAMP-insensitive step that can bypass Raf-1 | Q34450770 | ||
| Palmitoylation of p59fyn is reversible and sufficient for plasma membrane association | Q34671604 | ||
| Receptor regulation of G-protein palmitoylation | Q35135424 | ||
| Gsalpha contains an unidentified covalent modification that increases its affinity for adenylyl cyclase | Q36179486 | ||
| Signal transducing molecules and glycosyl-phosphatidylinositol-linked proteins form a caveolin-rich insoluble complex in MDCK cells | Q36232566 | ||
| Cysteine3 of Src family protein tyrosine kinase determines palmitoylation and localization in caveolae | Q36382857 | ||
| Reciprocal regulation of Gs alpha by palmitate and the beta gamma subunit | Q37045553 | ||
| Activation-induced subcellular redistribution of Gs alpha | Q37381937 | ||
| Myristoylation of an inhibitory GTP-binding protein alpha subunit is essential for its membrane attachment | Q37671954 | ||
| The role of palmitoylation of the guanine nucleotide binding protein G11 alpha in defining interaction with the plasma membrane | Q38291497 | ||
| Palmitoylation of a G protein alpha i subunit requires membrane localization not myristoylation | Q38301446 | ||
| N-terminally myristoylated Ras proteins require palmitoylation or a polybasic domain for plasma membrane localization | Q38306703 | ||
| Failure to myristoylate the alpha subunit of Gz is correlated with an inhibition of palmitoylation and membrane attachment, but has no affect on phosphorylation by protein kinase C. | Q38311141 | ||
| G-protein palmitoyltransferase activity is enriched in plasma membranes | Q38360176 | ||
| Influence of gamma subunit prenylation on association of guanine nucleotide-binding regulatory proteins with membranes | Q40240626 | ||
| The dynamic role of palmitoylation in signal transduction | Q40443876 | ||
| Lipid-modified, cysteinyl-containing peptides of diverse structures are efficiently S-acylated at the plasma membrane of mammalian cells | Q41182094 | ||
| Regulation of cellular signalling by fatty acid acylation and prenylation of signal transduction proteins | Q41260833 | ||
| Reversible palmitoylation of signaling proteins | Q41382874 | ||
| Activation and depalmitoylation of Gs alpha | Q41459257 | ||
| G protein beta gamma subunits synthesized in Sf9 cells. Functional characterization and the significance of prenylation of gamma | Q41594166 | ||
| A polybasic domain or palmitoylation is required in addition to the CAAX motif to localize p21ras to the plasma membrane | Q41718569 | ||
| Rapid plasma membrane anchoring of newly synthesized p59fyn: selective requirement for NH2-terminal myristoylation and palmitoylation at cysteine-3. | Q41838604 | ||
| Stimulation of phospholipase C-beta 2 by recombinant guanine-nucleotide-binding protein beta gamma dimers produced in a baculovirus/insect cell expression system. Requirement of gamma-subunit isoprenylation for stimulation of phospholipase C. | Q42068981 | ||
| Reconstitution of constitutive secretion using semi-intact cells: regulation by GTP but not calcium | Q43107643 | ||
| Adenovirus-mediated transfection of cultured cells. | Q46395331 | ||
| Fatty acylation of alpha z. Effects of palmitoylation and myristoylation on alpha z signaling | Q46429289 | ||
| Understanding covalent modifications of proteins by lipids: where cell biology and biophysics mingle | Q47896008 | ||
| Lipid modifications of G protein subunits. Myristoylation of Go alpha increases its affinity for beta gamma. | Q48770702 | ||
| Binding of acylated peptides and fatty acids to phospholipid vesicles: pertinence to myristoylated proteins | Q70480633 | ||
| Localization of epidermal growth factor-stimulated Ras/Raf-1 interaction to caveolae membrane | Q71142838 | ||
| Biochemical Characterization of a Palmitoyl Acyltransferase Activity That Palmitoylates Myristoylated Proteins | Q72055049 | ||
| Increased palmitoylation of the Gs protein alpha subunit after activation by the beta-adrenergic receptor or cholera toxin | Q72571513 | ||
| Doubly-lipid-modified protein sequence motifs exhibit long-lived anchorage to lipid bilayer membranes | Q72638453 | ||
| Roles of lipid modifications of transducin subunits in their GDP-dependent association and membrane binding | Q72773647 | ||
| Retargeting of cytosolic proteins to the plasma membrane by the Lck protein tyrosine kinase dual acylation motif | Q73202495 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | heterotrimeric G protein | Q408561 |
| signal transduction | Q828130 | ||
| P304 | page(s) | 1-14 | |
| P577 | publication date | 1998-01-01 | |
| P1433 | published in | Molecular Biology of the Cell | Q2338259 |
| P1476 | title | Plasma membrane localization of G alpha z requires two signals | |
| Plasma Membrane Localization of GαzRequires Two Signals | |||
| P478 | volume | 9 |
| Q28347801 | 5-Hydroxytryptamine 4(a) receptor expressed in Sf9 cells is palmitoylated in an agonist-dependent manner |
| Q28566717 | Activation of Gz attenuates Rap1-mediated differentiation of PC12 cells |
| Q40923011 | Activation of the beta(2)-adrenergic receptor-Galpha(s) complex leads to rapid depalmitoylation and inhibition of repalmitoylation of both the receptor and Galpha(s). |
| Q57371824 | Acylation-dependent Protein Export in Leishmania |
| Q43916214 | An Arabidopsis calcium-dependent protein kinase is associated with the endoplasmic reticulum |
| Q36845087 | Assembly and trafficking of heterotrimeric G proteins |
| Q39103381 | Caveolins and cavins in the trafficking, maturation, and degradation of caveolae: implications for cell physiology |
| Q33953511 | Cellular palmitoylation and trafficking of lipidated peptides |
| Q43757440 | Characterization of the functional heterologous desensitization of hypothalamic 5-HT(1A) receptors after 5-HT(2A) receptor activation. |
| Q37821600 | Chemical and genetic probes for analysis of protein palmitoylation |
| Q28239520 | Differential modulation of type 1 and type 2 cannabinoid receptors along the neuroimmune axis |
| Q33923711 | Discovery and characterization of inhibitors of human palmitoyl acyltransferases |
| Q40760010 | Dissecting Receptor–G Protein Specificity Using Gα Chimeras |
| Q38480070 | Dual lipid modification motifs in G(alpha) and G(gamma) subunits are required for full activity of the pheromone response pathway in Saccharomyces cerevisiae |
| Q57266282 | Eukaryotic Fatty Acylation Drives Plasma Membrane Targeting and Enhances Function of Several Type III Effector Proteins from Pseudomonas syringae |
| Q28769801 | Except in every detail: comparing and contrasting G-protein signaling in Saccharomyces cerevisiae and Schizosaccharomyces pombe |
| Q29618490 | Fatty acylation of proteins: new insights into membrane targeting of myristoylated and palmitoylated proteins |
| Q38614617 | Functional roles for fatty acylated amino-terminal domains in subcellular localization |
| Q38060611 | G Protein Trafficking |
| Q22253446 | Galpha 13 requires palmitoylation for plasma membrane localization, Rho-dependent signaling, and promotion of p115-RhoGEF membrane binding |
| Q27933909 | Galpha subunit Gpa2 recruits kelch repeat subunits that inhibit receptor-G protein coupling during cAMP-induced dimorphic transitions in Saccharomyces cerevisiae |
| Q41673440 | Gbetagamma and palmitate target newly synthesized Galphaz to the plasma membrane |
| Q48159206 | Golfalpha is expressed in primary sensory neurons outside of the olfactory neuroepithelium |
| Q90723620 | Gγ and Gα Identity Dictate a G-Protein Heterotrimer Plasma Membrane Targeting |
| Q52549569 | Heterotrimer formation, together with isoprenylation, is required for plasma membrane targeting of Gbetagamma |
| Q24604409 | Huntingtin interacting protein 14 is an oncogenic human protein: palmitoyl acyltransferase |
| Q57363778 | Identification of calcium binding sites in the trypanosome flagellar calcium-acyl switch protein |
| Q57371836 | Lipid-dependent Targeting of G Proteins into Rafts |
| Q33870605 | Lipid-linked proteins of plants |
| Q35004171 | Localization of a peripheral membrane protein: Gbetagamma targets Galpha(Z). |
| Q34061239 | Membrane trafficking of heterotrimeric G proteins via the endoplasmic reticulum and Golgi |
| Q33946075 | Mutant G protein alpha subunit activated by Gbeta gamma: a model for receptor activation? |
| Q39958282 | N-terminal polybasic motifs are required for plasma membrane localization of Galpha(s) and Galpha(q). |
| Q30973838 | Palmitoylation is required for membrane association of activated but not inactive invertebrate visual Gqalpha |
| Q28184264 | Palmitoylation regulates regulators of G-protein signaling (RGS) 16 function. I. Mutation of amino-terminal cysteine residues on RGS16 prevents its targeting to lipid rafts and palmitoylation of an internal cysteine residue |
| Q34810345 | Persistent membrane association of activated and depalmitoylated G protein alpha subunits |
| Q44263334 | Potentiation of GPCR-signaling via membrane targeting of G protein alpha subunits |
| Q36328401 | Protein palmitoylation in signal transduction of hematopoietic cells |
| Q28283407 | RGSZ1, a Gz-selective RGS protein in brain. Structure, membrane association, regulation by Galphaz phosphorylation, and relationship to a Gz gtpase-activating protein subfamily |
| Q28213744 | Regulation of G proteins by covalent modification |
| Q40891017 | Regulation of adenylyl cyclase, ERK1/2, and CREB by Gz following acute and chronic activation of the delta-opioid receptor |
| Q73807687 | Regulation of galpha i palmitoylation by activation of the 5-hydroxytryptamine-1A receptor |
| Q35031239 | Role of palmitoylation/depalmitoylation reactions in G-protein-coupled receptor function |
| Q40941453 | SNAP-25 is targeted to the plasma membrane through a novel membrane-binding domain. |
| Q77631481 | Signalling functions of protein palmitoylation |
| Q34147620 | Site-specific analysis of protein S-acylation by resin-assisted capture |
| Q34462319 | Specificity of plasma membrane targeting by the rous sarcoma virus gag protein |
| Q46217307 | Subcellular targeting of nine calcium-dependent protein kinase isoforms from Arabidopsis |
| Q40846847 | Targeting proteins to plasma membrane and membrane microdomains by N-terminal myristoylation and palmitoylation |
| Q57371805 | The Dually Acylated NH2-terminal Domain of Gi1αIs Sufficient to Target a Green Fluorescent Protein Reporter to Caveolin-enriched Plasma Membrane Domains |
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