| pubmed-article:2835009 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2835009 | lifeskim:mentions | umls-concept:C0034721 | lld:lifeskim |
| pubmed-article:2835009 | lifeskim:mentions | umls-concept:C0034693 | lld:lifeskim |
| pubmed-article:2835009 | lifeskim:mentions | umls-concept:C0205054 | lld:lifeskim |
| pubmed-article:2835009 | lifeskim:mentions | umls-concept:C0018328 | lld:lifeskim |
| pubmed-article:2835009 | lifeskim:mentions | umls-concept:C0061352 | lld:lifeskim |
| pubmed-article:2835009 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
| pubmed-article:2835009 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:2835009 | pubmed:dateCreated | 1988-6-2 | lld:pubmed |
| pubmed-article:2835009 | pubmed:abstractText | To investigate whether guanine nucleotides regulate interconversion of the two-state hepatic glucagon receptor we have utilized kinetic assays of glucagon binding to partially purified rat liver plasma membranes. Dissociation of glucagon at 30 degrees C exhibited biexponential character in either the absence or presence of GTP, indicating that the system previously seen in intact hepatocytes is independent of intracellular modulators. In each case the receptors underwent a time-dependent conversion from a low affinity to a high affinity state. However, GTP decreased the fraction of receptors in the high affinity state. The rank order for stabilizing the low affinity state was Gpp(NH)p greater than GTP greater than GDP much greater than GMP = no nucleotides. Data from competition binding assays with increasing concentrations of GTP allow calculation of equilibrium constants which are 3.32 nM for glucagon and receptor in the absence of GTP, 18.6 nM for glucagon and receptor in the presence of GTP, 1.55 microM for the association of receptor and GTP presumably linked to an N protein, and 8.86 microM for the association of the glucagon-receptor complex and GTP again presumably linked to an N protein, Glucagon binding to receptor is noncooperative in both the absence and presence of GTP, distinguishing this system from the beta-adrenergic system. With GTP, binding to the low affinity state is favored because of the relative affinities reported. Therefore, GTP regulates the activation by slowing the conversion of the receptor from a low affinity to high affinity form. | lld:pubmed |
| pubmed-article:2835009 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2835009 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2835009 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2835009 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:2835009 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2835009 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2835009 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2835009 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2835009 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2835009 | pubmed:month | May | lld:pubmed |
| pubmed-article:2835009 | pubmed:issn | 0003-9861 | lld:pubmed |
| pubmed-article:2835009 | pubmed:author | pubmed-author:JenkinsW TWT | lld:pubmed |
| pubmed-article:2835009 | pubmed:author | pubmed-author:KINGRR | lld:pubmed |
| pubmed-article:2835009 | pubmed:author | pubmed-author:MormolJ SJS | lld:pubmed |
| pubmed-article:2835009 | pubmed:author | pubmed-author:WyborskiR JRJ | lld:pubmed |
| pubmed-article:2835009 | pubmed:author | pubmed-author:HorwitzE MEM | lld:pubmed |
| pubmed-article:2835009 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2835009 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:2835009 | pubmed:volume | 262 | lld:pubmed |
| pubmed-article:2835009 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2835009 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2835009 | pubmed:pagination | 532-42 | lld:pubmed |
| pubmed-article:2835009 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:meshHeading | pubmed-meshheading:2835009-... | lld:pubmed |
| pubmed-article:2835009 | pubmed:year | 1988 | lld:pubmed |
| pubmed-article:2835009 | pubmed:articleTitle | Guanine nucleotide regulation of the interconversion of the two-state hepatic glucagon receptor system of rat. | lld:pubmed |
| pubmed-article:2835009 | pubmed:affiliation | Department of Chemistry, Indiana University, Bloomington 47405. | lld:pubmed |
| pubmed-article:2835009 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2835009 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2835009 | lld:pubmed |
