Zobrazeno 1 - 10
of 31
pro vyhledávání: '"R. T. Ogata"'
Publikováno v:
The Journal of Immunology. 158:3852-3860
To find protein-protein interactive sites in complement component C3, we examined regions of C3 that are proximal to sites of length polymorphism or indels in the C345 protein family. We reasoned that indels probably mark protein interactive sites be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b91c2c830196a37d58dbcb7130d21f9f
https://doi.org/10.4049/jimmunol.158.8.3852
https://doi.org/10.4049/jimmunol.158.8.3852
Publikováno v:
The Journal of Immunology. 154:2351-2357
Ra-reactive factor (RaRF) is a serum bactericidal factor whose function seems to be to activate C in a manner similar to that of C1, but with activation triggered by binding to bacterial polysaccharides instead of to immune complexes. It is composed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65bca2f47e5ee3376fd053881bda0f13
https://doi.org/10.4049/jimmunol.154.5.2351
https://doi.org/10.4049/jimmunol.154.5.2351
Publikováno v:
The Journal of Immunology. 152:5890-5895
An early step in the initiation of the classical C pathway is the proteolytic activation of component C4 by subcomponent C1-s. We have examined the substrate specificity of murine C1-s (mC1-s) by measuring its proteolytic activity on human and murine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b529091be1984bc000a568b761d26799
https://doi.org/10.4049/jimmunol.152.12.5890
https://doi.org/10.4049/jimmunol.152.12.5890
Murine C4b-binding protein. Mapping of the ligand binding site and the N-terminus of the pre-protein
Publikováno v:
The Journal of Immunology. 150:2273-2280
We have constructed cell surface-bound forms of murine C4b-binding protein (mC4BP) that allowed us to monitor the binding of mC4BP to C4b with relatively simple erythrocyte rosette assays. We used two types of surface-bound mC4BP: one in which segmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fe608601bc8df4a1da200632b14fd9b
https://doi.org/10.4049/jimmunol.150.6.2273
https://doi.org/10.4049/jimmunol.150.6.2273
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 162(11)
We recently suggested that sites of length polymorphisms in protein families (indels) might serve as useful guides for locating protein:protein interaction sites. This report describes additional site-specific mutagenesis and synthetic peptide inhibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52fe9ff3777de5db4d5f2041a4c6b437
https://pubmed.ncbi.nlm.nih.gov/10352274
https://pubmed.ncbi.nlm.nih.gov/10352274
Publikováno v:
Molecular and cellular biochemistry. 192(1-2)
The interactions of long chain fatty acids (FA) with wild type (WT) fatty acid binding proteins (FABP) and engineered FABP mutants have been monitored to determine the equilibrium binding constants as well as the rate constants for binding and dissoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e65f049dd4128b03774e3ab7ad34dd06
https://pubmed.ncbi.nlm.nih.gov/10331661
https://pubmed.ncbi.nlm.nih.gov/10331661
Publikováno v:
Molecular and cellular biochemistry. 192(1-2)
The aqueous phase monomers of fatty acids (FFA) appear in many steps of fat metabolism. Understanding metabolism requires that accurate measurements of FFA levels be determined in enzyme-mediated as well as in membrane and protein binding reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a9c192e7af19c1f401e6aee10d77b1d
https://pubmed.ncbi.nlm.nih.gov/10331662
https://pubmed.ncbi.nlm.nih.gov/10331662
Publikováno v:
The Journal of Immunology. 144:607-609
C4d.1 and C4d.2 are serologically defined allotypes of murine complement component C4. Previous studies in Shreffler's laboratory have shown that the structural difference between the two allotypes lies within a single tryptic peptide of the C4 alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ca1a5df4082bc1203faf43ddb86856d
https://doi.org/10.4049/jimmunol.144.2.607
https://doi.org/10.4049/jimmunol.144.2.607
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 161(9)
Engineered mutants of human complement component C3 were used to test the idea that sites of length polymorphisms in protein families (indels) can guide a search for protein:protein interaction sites. Sequence changes were introduced at each of the 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9428615346e2e11969dd94c0631e2b5f
https://pubmed.ncbi.nlm.nih.gov/9794410
https://pubmed.ncbi.nlm.nih.gov/9794410
Autor:
R T, Ogata, P J, Low
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 158(8)
To find protein-protein interactive sites in complement component C3, we examined regions of C3 that are proximal to sites of length polymorphism or indels in the C345 protein family. We reasoned that indels probably mark protein interactive sites be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9293b6cae457012fa925fb7b2eb1900
https://pubmed.ncbi.nlm.nih.gov/9103453
https://pubmed.ncbi.nlm.nih.gov/9103453