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Quantum Drug hit identification tool
Drug Hit Identification Tool calculates the IC50 (Kd, Ki, pKd) value of any protein-ligand complex, docks a small-molecule in the active site of a protein and performs screening a library of compounds against a target-protein or DNA/RNA. Hit Identification Tool consists of three modules: The IC50 module, 2) Ligand Docking and 3) Library Screening modules. Drug Hit Identification Tool can run both in Windows and Linux environments.
Hit Identification overview brochure![]()
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Title: Crystal structure of HLA-A2*0201 in complex with a decameric altered peptide ligand from the MART-1/Melan-A |
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Functional Class: Immune System Primary citation: Sliz, P.,Michielin, O.,Cerottini, J.C.,Luescher, I.,Romero, P.,Karplus, M.,Wiley, D.C. Crystal structures of two closely related but antigenically distinct HLA-A2/melanocyte-melanoma tumor-antigen peptide complexes. J.Immunol. v167 pp.3276-3284, 2001 |
Abstract Title: Crystal structures of two closely related but antigenically distinct HLA-A2/melanocyte-melanoma tumor-antigen peptide complexes.
Keywords: Research, (1jf1:a), (homo, Molecular, Sandwich, Ligand, Immunoglobulins, Presentation, D1jf1a2, D1jf1a1, Peptide, Alpha, Immunoglobulin, (1jf1:b), Alpha-1, Alpha-2, Alpha-3, Antigen, Proteins, 1jf1a2, T-lymphocytes, Activity, Protein, Sapiens, Domain, Binding, Sapiens),, Neoplasm, (1jf1:c), Fragments, Hla-a2.1, Chain, Substances, Water, Antigens, Macromolecular, Class, 1jf1a1, Immunoglobulin-like, U.s., Processing, Proteins, Mart-1/melan-, (antibody, Histocompatibility, Peptide, Beta2-microglobulin, Chain, Homo, Human, Domains, Gov't, X-ray, Amino, Synthetic, Pliability, Melanoma, Support, Receptor, Construct, From, Models, (a+b), Conformation, Antigen,, Beta, Sapiens), Antigen, Decameric, Cytotoxic, 2-layer, Like), Hla-a2, Mainly, Study, Comparative, Crystallography, Constant, Sites, Complex,, Zinc, Protein, Complex, Non-p.h.s., Beta-sandwich, Subunit, Class, Beta-2-microglobulin, Murine, Mhc,, Beta, P.h.s., Class, Major, Antigen-recognition, Domain-, Sequence, Humans, D1jf1b_, 1jf1b0, Histocompatibility, Alpha, Acid, Desriptors, Training set, In silico, Studies, Development, Assessment, Scoring function, Low-frequency normal modes, Degrees of freedom, Geometry refinement (optimization), Investigation, Computation of lowest-frequency modes of, Binding energy prediction, Conformational flexibility, Pharmacophore, Three-dimensional quantitative structure activity relationship methods, Conformational analysis, Profiling, ,







