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EC Number
Title
Organism
3.4.23.16
A substrate selected by phage display exhibits enhanced side-chain hydrogen bonding to HIV-1 protease
Human immunodeficiency virus 1
3.4.23.16
An inhibitor of HIV-1 protease modulates constitutive eIF2alpha dephosphorylation to trigger a specific integrated stress response
Human immunodeficiency virus 1
3.4.23.16
Binding kinetics and substrate selectivity in HIV-1 protease-Gag interactions probed at atomic resolution by chemical exchange NMR
Human immunodeficiency virus 1
3.4.23.16
Conformations of the HIV-1 protease A crystal structure data set analysis
Human immunodeficiency virus 1
3.4.23.16
Developing HIV-1 protease inhibitors through stereospecific reactions in protein crystals
Human immunodeficiency virus 1
3.4.23.16
Effects of drug-resistant mutations on the dynamic properties of HIV-1 protease and inhibition by amprenavir and darunavir
Human immunodeficiency virus 1
3.4.23.16
Exploration of the effect of sequence variations located inside the binding pocket of HIV-1 and HIV-2 proteases
Human immunodeficiency virus 1
3.4.23.16
Exploring the reasons for decrease in binding affinity of HIV-2 against HIV-1 protease complex using interaction entropy under polarized force field
Human immunodeficiency virus 1
3.4.23.16
Highly drug-resistant HIV-1 protease mutant PRS17 shows enhanced binding to substrate analogues
Human immunodeficiency virus 1
3.4.23.16
HIV-1 protease substrate-groove Role in substrate recognition and inhibitor resistance
Human immunodeficiency virus 1
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