The Biomolecular Interaction Network Database (BIND) (http://bind.ca) archives biomolecular interaction, reaction, complex and pathway information. Our aim is to curate the details about molecular interactions that arise from published experimental research and to provide this information, as well as tools to enable data analysis, freely to researchers worldwide. BIND data are curated into a comprehensive machinereadable archive of computable information and provides users with methods to discover interactions and molecular mechanisms. BIND has worked to develop new methods for visualization that amplify the underlying annotation of genes and proteins to facilitate the study of molecular interaction networks. BIND has maintained an open database policy since its inception in 1999. Data growth has proceeded at a tremendous rate, approaching over 100 000 records. New services provided include a new BIND Query and Submission interface, a Standard Object Access Protocol service and the Small Molecule Interaction Database (http://smid.blueprint.org) that allows users to determine probable small molecule binding sites of new sequences and examine conserved binding residues. INTRODUCTIONIn light of the vast scientific resources made available through genomics, the science of deciphering molecular mechanisms is expanding rapidly. Scientists who once hunted for disease genes or sought to distinguish key concepts in evolution are now turning their attention to the details of molecular assembly and mechanism to further understand medicine and the key concepts underlying biology. The Biomolecular Interaction Network Database (BIND) was designed to store complete information about molecular assembly through a database structure in order to archive interactions and reactions arising from biopolymers (protein, RNA and DNA), as well as small molecules, lipids and carbohydrates. Detailed information about molecular mechanism, such as the chemical product(s) of an enzymatic reaction, can be encoded in BIND. The underlying ontology of the BIND database is chemistry, and as such, BIND is capable of storing information about molecular interactions to atomic resolution. The taxonomic scope of BIND is

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We have performed extensive zero field µSR experiments on pure YBa2Cu3O6+y and diluted Yrare-earth substituted Y0.92Eu0.08Ba2Cu3O6+y and Y0.925Nd0.075Ba2Cu3O6+y at light hole-doping. A common magnetic behavior is detected for all the three families, demonstrating negligible effects of the isovalent Y-substituent disorder. Two distinct regimes are identified, separated by a crossover, whose origin is attributed to the concurrent thermal activation of spin and charge degrees of freedom: a thermally activated and a re-entrant antiferromagnetic regime. The peculiar temperature and hole density dependence of the magnetic moment m(h, T ) fit a model with a (spin) activation energy for the crossover between the two regimes throughout the entire investigated range. The magnetic moment is suppressed by a simple dilution mechanism both in the re-entrant regime (0 ≤ h ≤ 0.056) and in the so-called Cluster Spin Glass state coexisting with superconductivity (0.056 < h 0.08). We argue a common magnetic ground state for these two doping regions and dub it frozen antiferromagnet. Conversely either frustration or finite-size effects prevail in the thermally activated antiferromagnetic state, that vanishes at the same concentration where superconductivity emerges, suggesting the presence of a quantum critical point at hc = 0.056(2).

A plum pudding-like Fe(3)O(4)/Fe/carbon composite was synthesized by a sol-gel polymerization followed by a heat-treatment process and characterized by X-ray diffraction, Raman spectroscopic analysis, thermogravimetric analysis, scanning electron microscopy with energy-dispersive spectroscopy, transmission electron microscopy, and electrochemical test. In this composite, uniform spherical Fe(3)O(4)/Fe nanoparticles of about 100 nm were embedded into carbon matrix with high monodispersion. As-prepared Fe(3)O(4)/Fe/carbon composite electrode exhibits a stable and reversible capacity of over 600 mA h g(-1) at a current of 50 mA g(-1) between 0.002 V and 3.0 V, as well as excellent rate capability. The plum pudding-like structure, in which trace Fe promotes conductivity and carbon matrix mediates the volume change, can enhance the cycling performance and rate capability of Fe(3)O(4) electrode. This unique structure is valuable for the preparation of other electrode materials.