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Identification of binding sites and favorable ligand binding moieties by virtual screening and self-organizing map analysis

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Identifying druggable cavities on a protein surface is a crucial step in structure based drug design. The cavities have to present suitable size and shape, as well as appropriate chemical complementarity with ligands. |

TÀI LIỆU LIÊN QUAN

Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection

Genome-wide identification and expression analysis of the calmodulin-binding transcription activator (CAMTA) gene family in wheat (Triticum aestivum L.)

Analyses on clustering of the conserved residues at protein-RNA interfaces and its application in binding site identification

Identification of binding sites and favorable ligand binding moieties by virtual screening and self-organizing map analysis

NDNA-prot: Identification of DNA-binding proteins based on unbalanced classification

Identification of dual histone modification-binding protein interaction by combining mass spectrometry and isothermal titration calorimetric analysis

Identification of DNA-binding proteins using multi-features fusion and binary firefly optimization algorithm

Identification of high-confidence RNA regulatory elements by combinatorial classification of RNA–protein binding sites

Báo cáo y học: "Evaluation of the sensitization rates and identification of IgE-binding components in wild and genetically modified potatoes in patients with allergic disorders"

Báo cáo y học: " Identification of biomolecule mass transport and binding rate parameters in living cells by inverse modeling"