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HIV-1 PR resistant mutant + LPV
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2023-08-30
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Investigation of novel indole-based HIV-1 protease inhibitors using virtual screening and text mining
Human immunodeficiency virus type 1 protease (HIV-1 PR) inhibitors have been used as possible therapeutic agents for HIV-1 infection in clinical study. Most of the HIV therapy-related problems usually
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HIV-1 Protease WT (NL4-3) in Complex with PU1 (LR3-46)
HIV-1 Protease WT (NL4-3) in Complex with PU1 (LR3-46)
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HIV-1 Protease WT (NL4-3) in Complex with LR4-33
HIV-1 Protease WT (NL4-3) in Complex with LR4-33
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Crystal Structure of wild-type HIV-1 Protease in Complex with MKP97
Crystal Structure of wild-type HIV-1 Protease in Complex with MKP97 Descriptor: PHOSPHATE ION, Pol polyprotein, [(2S)-5-oxopyrrolidin-2-yl]methyl [(2S,3R)-4-{(1,3-benzothiazol-6-ylsulfonyl)[(2S)-2-met
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Crystal Structure of HIV-1 Protease (Q7K, L33I, L63I) in Complex with KNI-10006
Crystal Structure of HIV-1 Protease (Q7K, L33I, L63I) in Complex with KNI-10006 Descriptor: (4R)-3-[(2S,3S)-3-{[(2,6-dimethylphenoxy)acetyl]amino}-2-hydroxy-4-phenylbutanoyl]-N-[(1S,2R)-2-hydroxy-2,3-
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