EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
6.2.1.45 | ATP + ubiquitin + [E1 ubiquitin-activating enzyme]-L-cysteine |
- |
Arabidopsis thaliana |
AMP + diphosphate + S-ubiquitinyl-[E1 ubiquitin-activating enzyme]-L-cysteine |
- |
? |
6.2.1.45 | ATP + ubiquitin + [ubiquitin-activating protein UBA1]-L-cysteine |
enzyme forms higher molecular mass intermediates with ubiquitin |
Arabidopsis thaliana |
AMP + diphosphate + [ubiquitin-activating protein UBA1]-S-ubiquitinyl-L-cysteine |
the enzyme-ubiquitin intermediates dissociate in presence of 2-mercaptoethanol, indicating thiolester linkage |
? |
6.2.1.45 | ATP + ubiquitin + [ubiquitin-activating protein UBA2]-L-cysteine |
enzyme forms higher molecular mass intermediates with ubiquitin |
Arabidopsis thaliana |
AMP + diphosphate + [ubiquitin-activating protein UBA2]-S-ubiquitinyl-L-cysteine |
the enzyme-ubiquitin intermediates dissociate in presence of 2-mercaptoethanol, indicating thiolester linkage |
? |
6.2.1.45 | ATP + ubiquitin + [ubiquitin-activating protein E1]-L-cysteine |
- |
Bos taurus |
AMP + diphosphate + [ubiquitin-activating protein E1]-S-ubiquitinyl-L-cysteine |
- |
? |
6.2.1.45 | ATP + ubiquitin mutant G76A + [ubiquitin-activating protein E1]-L-cysteine |
- |
Bos taurus |
AMP + diphosphate + [ubiquitin-activating protein E1]-S-(ubiquitin mutant G76A)yl-L-cysteine |
mutant ubiquitin G76A, bearing a Gly to Ala substitution at the COOH terminus is a substrate for El enzyme. Ubiquitin G76A supports PPI-ATP exchange with 500fold decrease in kcat/Km compared to wild-type ubiquitin, does not produce detectable AMP-Ub with native El, produces stoichiometric AMP-Ub with thiol-blocked El, gives a stoichiometric burst of ATP consumption with either native or thiol-blocked El, support El-ubiquitin thiol ester formation with native El, and supports several downstream reactions of the proteolytic pathway with a 20% decrease to the rate of wild type ubiquitin |
? |
6.2.1.45 | ATP + ubiquitin + [E1 ubiquitin-activating enzyme]-L-cysteine |
- |
Citrus reticulata |
AMP + diphosphate + S-ubiquitinyl-[E1 ubiquitin-activating enzyme]-L-cysteine |
- |
? |
6.2.1.45 | ATP + ubiquitin + [E1 ubiquitin-activating enzyme]-L-cysteine |
- |
Drosophila melanogaster |
AMP + diphosphate + S-ubiquitinyl-[E1 ubiquitin-activating enzyme]-L-cysteine |
- |
? |
6.2.1.45 | ATP + ubiquitin + [ubiquitin-activating protein E1]-L-cysteine |
a carboxylgroup is first activated as an adenylate followed by its direct transfer to an autonomous molecular moiety in a single enzymatic step |
Escherichia coli |
AMP + diphosphate + [ubiquitin-activating protein E1]-S-ubiquitinyl-L-cysteine |
- |
? |
6.2.1.45 | more |
a lysine 48-linked polyubiquitin chain, assembled upon an internal lysine residue of a substrate protein, becomes the principle signal for recognition and target degradation by the 26S proteasome. E1 is not only essential for the initial ATP-dependent activation of ubiquitin in the ubiquitin degradtion pathway, but also capable of the catalytic extension of the polyubiquitin chain on a mono-ubiquitinated substrate |
Escherichia coli |
? |
- |
? |
6.2.1.45 | ATP + ubiquitin + [E1 ubiquitin-activating enzyme]-L-cysteine |
- |
Giardia intestinalis |
AMP + diphosphate + S-ubiquitinyl-[E1 ubiquitin-activating enzyme]-L-cysteine |
- |
? |