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MMDB Description
73437Hiv-1 Protease in Complex With Sdz283-910
12513Counteracting Hiv-1 Protease Drug Resistance: Structural Analysis of Mutant Proteases Complexed With Xv638 and Sd146, Cyclic Urea Amides With Broad Specificities
19723Hiv-1 Protease in Complex With the Inhibitor Bea369
73646Crystal Structure of a Complex of Hiv-1 Protease With a Dihydroethylene-containing Inhibitor: Comparisons With Molecular Modeling
1289Structural Basis of Drug Resistance for the V82a Mutant of Hiv-1 Protease: Backbone Flexibility and Subsite Repacking
49549Hiv-1 Proteinase Complexed With RO 31-8959
7007Hiv-1 Protease Dimer Complexed With A-84538
21361Inhibitor of HIV Protease With Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants
21362Inhibitor of HIV Protease With Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants
7495Hiv-1 Mutant (V82f) Protease Complexed With Dmp323
50612Native Hiv-1 Proteinase
50613Hiv-1 Proteinase Mutant A71t, V82a
4836Hiv-1 Protease Dimer Complexed With A-98881
2155An Orally-bioavailable Hiv-1 Protease Inhibitor Containing an Imidazole-derived Peptide Bond Replacement. Crystallographic and Pharmacokinetic Analysis
9368Hiv-1 Protease Complexed With the Inhibitor Hoebay 793 Hexagonal Form
9073Hiv-1 Protease Complexed With the Inhibitor Hoebay 793 Orthorhombic Form
52538Hiv-1 Protease Nl4-3 1X Mutant
52539Hiv-1 Protease Nl4-3 3X Mutant in Complex With Inhibitor, Tl-3
58047Three-dimensional Structure of Aspartyl Protease From Human Immunodeficiency Virus Hiv-1
65553Crystal Structure of Hiv-1 Protease Complexed With Pl-100
66403I50v Hiv-1 Protease Mutant in Complex With a Carbamoyl Decorated Pyrrolidine-based Inhibitor
66548I50v Hiv-1 Protease in Complex With an Amino Decorated Pyrrolidine- Based Inhibitor
83066HIV Protease Complexed With Compound 10B
3200X-ray Crystal Structure of the HIV Protease Complex With L- 700,417, an Inhibitor With Pseudo C2 Symmetry
54778Crystallographic Analysis of a Complex Between Human Immunodeficiency Virus Type 1 Protease and Acetyl- Pepstatin at 2.0-angstroms Resolution
54880Design, Activity and 2.8 Angstroms Crystal Structure of a C2 Symmetric Inhibitor Complexed to Hiv-1 Protease