Journal article
NMR Structures Reveal How Oxidation Inactivates Thrombomodulin †
Abstract
Oxidation of Met 388, one of the three linker residues connecting the fourth and fifth EGF-like domains of thrombomodulin (TM), is deleterious for TM activity. An NMR structure of the smallest active fragment of TM (TMEGF45) and a crystal structure of a larger fragment (TMEGF456) bound to thrombin both show that Met 388 is packed into the fifth domain. Using multidimensional NMR, we have solved the structure of TMEGF45 in which Met 388 is …
Authors
Wood MJ; Becvar LA; Prieto JH; Melacini G; Komives EA
Journal
Biochemistry, Vol. 42, No. 41, pp. 11932–11942
Publisher
American Chemical Society (ACS)
Publication Date
October 1, 2003
DOI
10.1021/bi034646q
ISSN
0006-2960
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Amino Acid SequenceEnzyme ActivationEpidermal Growth FactorHumansKineticsLeucineMethionineModels, MolecularMolecular Sequence DataMutagenesis, Site-DirectedNuclear Magnetic Resonance, BiomolecularOxidation-ReductionPeptide FragmentsProtein BindingProtein CProtein Structure, TertiaryStructure-Activity RelationshipThrombinThrombomodulin