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Literature summary for 3.4.23.16 extracted from

  • Miller, M.; Schneider, J.; Sathyanarayana, B.K.; Toth, M.V.; Marshall, G.R.; Clawson, L.; Selk, L.; Kent, S.B.H.; Wlodawer, A.
    Structure of complex of synthetic HIV-1 protease with a substrate-based inhibitor at 2.3 A resolution (1989), Science, 246, 1149-1152.
    View publication on PubMed

Crystallization (Commentary)

Crystallization (Comment) Organism
crystallization of a complex between the chemically synthesized HIV-1 protease and the peptide inhibitor N-acetyl-Thr-Ile-Nle-PSI[CH2-NH]-Nle-Gln-Arg-amide Human immunodeficiency virus 1

Inhibitors

Inhibitors Comment Organism Structure
MVT-101
-
Human immunodeficiency virus 1

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
1.4
-
Ac-TIMMQR-NH2
-
Human immunodeficiency virus 1

Organism

Organism UniProt Comment Textmining
Human immunodeficiency virus 1
-
the enzyme is chemically synthesized
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
Ac-TIMMQR-NH2 + H2O
-
Human immunodeficiency virus 1 Ac-TIM + MQR-NH2
-
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