Inhibitors | Comment | Organism | Structure |
---|---|---|---|
N-(tert-butoxycarbonyl)-L-valyl-N-[(1R)-1-(diphenoxyphosphoryl)-2-methylpropyl]prolinamide | i.e. JO146. Inhibition during the replicative phase results in significant loss of viable infectious progeny | Chlamydia pecorum | |
N-(tert-butoxycarbonyl)-L-valyl-N-[(1R)-1-(diphenoxyphosphoryl)-2-methylpropyl]prolinamide | i.e. JO146. Inhibition during the replicative phase results in significant loss of viable infectious progeny | Chlamydia suis | |
N-(tert-butoxycarbonyl)-L-valyl-N-[(1R)-1-(diphenoxyphosphoryl)-2-methylpropyl]prolinamide | i.e. JO146. Inhibition during the replicative phase results in significant loss of viable infectious progeny | Chlamydia trachomatis |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Chlamydia pecorum | - |
- |
- |
Chlamydia suis | - |
- |
- |
Chlamydia trachomatis | - |
- |
- |
General Information | Comment | Organism |
---|---|---|
physiological function | Chlamydia trachomatis isolates with distinct replicative phase growth kinetics show significant loss of viable infectious progeny after HtrA is inhibited during the replicative phase | Chlamydia trachomatis |