| pubmed-article:18172 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18172 | lifeskim:mentions | umls-concept:C0010749 | lld:lifeskim |
| pubmed-article:18172 | lifeskim:mentions | umls-concept:C0022262 | lld:lifeskim |
| pubmed-article:18172 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
| pubmed-article:18172 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
| pubmed-article:18172 | lifeskim:mentions | umls-concept:C0030012 | lld:lifeskim |
| pubmed-article:18172 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:18172 | pubmed:dateCreated | 1977-9-22 | lld:pubmed |
| pubmed-article:18172 | pubmed:abstractText | The rate of reaction of ferro- and ferricytochrome c (C(II) and C(III) with ferri- and ferrocyanide and of C(III) with 02- and CO2- was determined in H2O and in 2H2O in the temperature range 5-35 degrees C. No isotope effect was evident in any of the reductions of C(III); the apparent energy of activation was identical in H2O and 2H2O. An isotope effect with kH2O/k2H2O = 1.25 to 1.85, depending on pH for instance was observed in the oxidation of C(II), in the slow phase of oxidation which involves conformational changes. An interpretation (supported by evidence from previous work) involving water molecules in the close vicinity of the reaction site on the protein is discussed. | lld:pubmed |
| pubmed-article:18172 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18172 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18172 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18172 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:18172 | pubmed:issn | 0006-3002 | lld:pubmed |
| pubmed-article:18172 | pubmed:author | pubmed-author:SteinGG | lld:pubmed |
| pubmed-article:18172 | pubmed:author | pubmed-author:IlanYY | lld:pubmed |
| pubmed-article:18172 | pubmed:author | pubmed-author:ShinarRR | lld:pubmed |
| pubmed-article:18172 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18172 | pubmed:day | 7 | lld:pubmed |
| pubmed-article:18172 | pubmed:volume | 461 | lld:pubmed |
| pubmed-article:18172 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18172 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18172 | pubmed:pagination | 15-24 | lld:pubmed |
| pubmed-article:18172 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Hy... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Ox... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Te... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Ca... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Ox... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-De... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Fe... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Ki... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Fe... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Fe... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Fe... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Pr... | lld:pubmed |
| pubmed-article:18172 | pubmed:meshHeading | pubmed-meshheading:18172-Cy... | lld:pubmed |
| pubmed-article:18172 | pubmed:year | 1977 | lld:pubmed |
| pubmed-article:18172 | pubmed:articleTitle | H/2H isotope effect in redox reactions of cytochrome c. | lld:pubmed |
| pubmed-article:18172 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18172 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
