The electron density map at the di-nuclear active site of AgPPO8. The electron densities of 2Fo-Fc map and Fo-Fc difference map are contoured at the sigma level of 1.0 and 3.0, and shown as gray and green mesh, respectively. (TIF 3813 kb
P. falciparum -infected RBCs did not significantly alter midgut bacterial growth relative to uninfec...
Table S2. A catalogue of midgut proteins identified using in-solution digestion strategy and LC/MS/M...
PPO3 does not contribute to hemolymph PO activity. Hemolymph PO activity of unchallenged larvae was ...
Characterization of the purified AgPPO8 wild type (WT) and E364Q mutant proteins. (A) SDS-PAGE analy...
AgPPO8 exists as a homodimer in solution. (A) AgPPO8 appears as dimeric on size exclusion chromatogr...
Docking of substrates to the Site II pocket of AgPPO8. (A) The binding energy for each individually ...
Docking analysis of phenolic substrates into the F99-deleted AgPPO8 active site. The docked active s...
from Anopheles gambiae provides new insights into the mechanism of PPO activation Yingxia Hu1, Yang ...
Background: Phenoloxidase (PO)-catalyzed melanization is a universal defense mechanism of insects ag...
Insect prophenoloxidase (PPO) is an important innate immunity protein due to its involvement in cell...
Comparative genomics of the PPO3 locus. Shown are the best pairwise genome alignments for 22 Drosoph...
Survival analysis after Leptopilina clavipes and L. boulardi wasp infestation in wild type and PPO m...
P. falciparum parasite products ( Pf Ps) induced A s P38 MAPK phosphorylation in vitro relative to c...
Table S1. Activity of PO and proPO in Meccus pallidipennis, according to hemolymph or anterior midgu...
Figure S10 Structural representation of the newly found motifs adhering near the binding pockets (sh...
P. falciparum -infected RBCs did not significantly alter midgut bacterial growth relative to uninfec...
Table S2. A catalogue of midgut proteins identified using in-solution digestion strategy and LC/MS/M...
PPO3 does not contribute to hemolymph PO activity. Hemolymph PO activity of unchallenged larvae was ...
Characterization of the purified AgPPO8 wild type (WT) and E364Q mutant proteins. (A) SDS-PAGE analy...
AgPPO8 exists as a homodimer in solution. (A) AgPPO8 appears as dimeric on size exclusion chromatogr...
Docking of substrates to the Site II pocket of AgPPO8. (A) The binding energy for each individually ...
Docking analysis of phenolic substrates into the F99-deleted AgPPO8 active site. The docked active s...
from Anopheles gambiae provides new insights into the mechanism of PPO activation Yingxia Hu1, Yang ...
Background: Phenoloxidase (PO)-catalyzed melanization is a universal defense mechanism of insects ag...
Insect prophenoloxidase (PPO) is an important innate immunity protein due to its involvement in cell...
Comparative genomics of the PPO3 locus. Shown are the best pairwise genome alignments for 22 Drosoph...
Survival analysis after Leptopilina clavipes and L. boulardi wasp infestation in wild type and PPO m...
P. falciparum parasite products ( Pf Ps) induced A s P38 MAPK phosphorylation in vitro relative to c...
Table S1. Activity of PO and proPO in Meccus pallidipennis, according to hemolymph or anterior midgu...
Figure S10 Structural representation of the newly found motifs adhering near the binding pockets (sh...
P. falciparum -infected RBCs did not significantly alter midgut bacterial growth relative to uninfec...
Table S2. A catalogue of midgut proteins identified using in-solution digestion strategy and LC/MS/M...
PPO3 does not contribute to hemolymph PO activity. Hemolymph PO activity of unchallenged larvae was ...