Inhibitors | Comment | Organism | Structure |
---|---|---|---|
2',3'-dideoxy-3'-(gamma-aminobutyric acid)amino thymidine | - |
Bos taurus | |
2',3'-dideoxy-3'-D-leucylamino thymidine | - |
Bos taurus | |
2',3'-dideoxy-3'-glycylamino thymidine | - |
Bos taurus | |
2',3'-dideoxy-3'-L-alanylamino thymidine | - |
Bos taurus | |
2',3'-dideoxy-3'-L-histidinylamino thymidine | - |
Bos taurus | |
2',3'-dideoxy-3'-L-leucylamino thymidine | - |
Bos taurus | |
2',3'-dideoxy-3'-L-serinylamino thymidine | occupies the active site of ribonuclease A and preferential perturbs the pKa value of His-119 by its free amino group as found from 1H NMR studies, compounds with polar amino acid side chains such as Ser-aT, Tyr-aT and Trp-aT (except His-aT) are more efficient inhibitors compared to those having hydrophobic side chains | Bos taurus | |
2',3'-dideoxy-3'-L-tryptophanylamino thymidine | compounds with polar amino acid side chains such as Ser-aT, Tyr-aT and Trp-aT (except His-aT) are more efficient inhibitors compared to those having hydrophobic side chains | Bos taurus | |
2',3'-dideoxy-3'-L-tyrosylamino thymidine | compounds with polar amino acid side chains such as Ser-aT, Tyr-aT and Trp-aT (except His-aT) are more efficient inhibitors compared to those having hydrophobic side chains | Bos taurus | |
2',3'-dideoxy-3'-L-valinylamino thymidine | - |
Bos taurus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Bos taurus | P61823 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
commercial preparation | - |
Bos taurus | - |
Synonyms | Comment | Organism |
---|---|---|
ribonuclease A | - |
Bos taurus |
RNase A | - |
Bos taurus |
Ki Value [mM] | Ki Value maximum [mM] | Inhibitor | Comment | Organism | Structure |
---|---|---|---|---|---|
0.08 | - |
2',3'-dideoxy-3'-L-serinylamino thymidine | - |
Bos taurus | |
0.451 | - |
2',3'-dideoxy-3'-L-tyrosylamino thymidine | - |
Bos taurus |