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The adsorption site of methoxy and ethoxy on Cu(100) as determined by vibrational spectroscopy and first principle calculations

Response of six European forest sites to decided and proposed air pollutant emission reductions

Analysis of regulatory phosphorylation sites in ZAP-70 by capillary high-performance liquid chromatography coupled to electrospray ionization or matrix-assisted laser desorption ionization time-of-flight mass spectrometry

Dynamics of water molecules in the active-site cavity of human cytochromes P450

Identification of Csk tyrosine phosphorylation sites and a tyrosine residue important for kinase domain structure

Redox potentials of the blue copper sites of bilirubin oxidases

Site-level model intercomparison of high latitude and high altitude soil thermal dynamics in tundra and barren landscapes

Ionization-site effects on the photofragmentation of chloro- and bromoacetic acid molecules

Simulation of CO2 and Attribution Analysis at Six European Peatland Sites Using the ECOSSE Model

Comparison of Methods to Obtain Force-Field Parameters for Metal Sites

Variability in exchange of CO2 across 12 northern peatland and tundra sites

A new route towards colloidal molecules with externally tunable interaction sites.

Bark lesions on beech (Fagus sylvatica) and their relation to epiphytes and site variables in Scania, south Sweden.

Structural and energetic characteristics of the heparin-binding site in antithrombotic protein C

N-unsubstituted glucosamine in heparan sulfate of recycling glypican-1 from suramin-treated and nitrite-deprived endothelial cells. mapping of nitric oxide/nitrite-susceptible glucosamine residues to clustered sites near the core protein

We have analyzed the content of N-unsubstituted glucosamine in heparan sulfate from glypican-1 synthesized by endothelial cells during inhibition of (a) intracellular progression by brefeldin A, (b) heparan sulfate degradation by suramin, and/or (c) endogenous nitrite formation. Glypican-1 from brefeldin A-treated cells carried heparan sulfate chains that were extensively degraded by nitrous acid

Nickel Complexes of Carboxylate-Containing Polydentate Ligands as Models for the Active Site of Urease

Identification of autoantibodies in human plasma recognizing an apoB-100 LDL receptor binding site peptide

Soil microbial activity in eleven Swedish coniferous forests in relation to site fertility and nitrogen fertilization

Bordetella pertussis binds to human C4b-binding protein (C4BP) at a site similar to that used by the natural ligand C4b

Human complement regulators are important targets for pathogenic microorganisms. In one such interaction, Bordetella pertussis binds human C4b-binding protein (C4BP), a high-molecular-weight plasma protein that acts as inhibitor of the classical pathway of complement activation. At least two different B. pertussis surface components, one of which is the virulence factor filamentous hemagglutinin (

MAGIC, SAFE and SMART model applications at integrated monitoring sites: Effects of emission reduction scenarios