Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
31
pubmed:dateCreated
1989-11-28
pubmed:abstractText
Replacement of the aspartate residue at position 59 of rat oncomodulin by glutamate by oligonucleotide-directed mutagenesis has afforded a protein which more closely resembles rat parvalbumin, at least judged by its interaction with the luminescent lanthanide ion Eu3+. The single-peak 7F0----5D0 spectrum observed at pH 5.0 with the fully bound wild-type protein is replaced by one which clearly shows two features at 5791 and 5796 A, arising from Eu3+ ions bound at the CD and EF sites, respectively. Furthermore, the pH dependence of the spectrum is substantially altered; the pKa observed for the CD domain, in which aspartate 59 residues, is shifted upward from pH 6.0 for the wild-type recombinant protein to pH 6.8 in the D59E mutant. Moreover, the maximum in the high-pH spectrum is shifted from 5781 to 5784 A. All three changes are indicative of a CD binding domain having increased parvalbumin-like character. Interestingly, however, the D59E substitution has only a modest effect on the Ca2+- and Mg2+-binding properties of the CD domain. For the wild-type protein, KCa = 7.8 x 10(-7) M and KMg = 3 x 10(-3) M. These affinities are more than an order of magnitude weaker than those seen for various parvalbumins and substantiate previous claims for calcium specificity made for the oncomodulin CD domain. Replacement of aspartate 59 by glutamate resulted in minor increases in affinity of the CD domain for Ca2+ (KCa = 5.5 x 10(-7) M) and Mg2+ (KMg = 1 x 10(-3) M). These findings strongly suggest that residues in oncomodulin besides aspartate 59 are important determinants of the observed calcium specificity of the CD calcium-binding domain. The consequences of the substitution at residue 59 appear to be confined to the CD domain. For the EF site in wild-type recombinant oncomodulin, KCa = 4.2 x 10(-8) M and KMg = 1.6 x 10(-4) M. The corresponding values for the D59E site-specific variant are identical within experimental error (KCa = 4.2 x 10(-8) M and KMg = 1.8 x 10(-4) M).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aspartic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Recombinant, http://linkedlifedata.com/resource/pubmed/chemical/DNA Restriction Enzymes, http://linkedlifedata.com/resource/pubmed/chemical/Europium, http://linkedlifedata.com/resource/pubmed/chemical/Glutamates, http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Magnesium, http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/oncomodulin
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
264
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
18751-60
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:2572594-Animals, pubmed-meshheading:2572594-Aspartic Acid, pubmed-meshheading:2572594-Calcium, pubmed-meshheading:2572594-Calcium-Binding Proteins, pubmed-meshheading:2572594-Cloning, Molecular, pubmed-meshheading:2572594-DNA, pubmed-meshheading:2572594-DNA, Recombinant, pubmed-meshheading:2572594-DNA Restriction Enzymes, pubmed-meshheading:2572594-Escherichia coli, pubmed-meshheading:2572594-Europium, pubmed-meshheading:2572594-Gene Expression, pubmed-meshheading:2572594-Glutamates, pubmed-meshheading:2572594-Glutamic Acid, pubmed-meshheading:2572594-Hydrogen-Ion Concentration, pubmed-meshheading:2572594-Luminescent Measurements, pubmed-meshheading:2572594-Magnesium, pubmed-meshheading:2572594-Mutation, pubmed-meshheading:2572594-Neoplasm Proteins, pubmed-meshheading:2572594-Nucleic Acid Hybridization, pubmed-meshheading:2572594-RNA, Messenger, pubmed-meshheading:2572594-Rats, pubmed-meshheading:2572594-Recombinant Proteins, pubmed-meshheading:2572594-Spectrophotometry, Ultraviolet
pubmed:year
1989
pubmed:articleTitle
Site-specific substitution of glutamate for aspartate at position 59 of rat oncomodulin.
pubmed:affiliation
Department of Chemistry, New Mexico State University, Las Cruces 88003.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't