EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
4.2.2.2 | Anemia, Hypochromic |
10882531 |
Induction of lytic enzymes by the interaction of Ustilago maydis with Zea mays tissues. |
unassigned |
0 |
4.2.2.2 | Coinfection |
20064057 |
Arabidopsis thaliana cells: a model to evaluate the virulence of Pectobacterium carotovorum. |
ongoing research unassigned |
4 0 |
4.2.2.2 | Cysts |
20507498 |
Molecular characterization and functional importance of pectate lyase secreted by the cyst nematode Heterodera schachtii. |
diagnostic usage ongoing research unassigned |
3 2 0 |
4.2.2.2 | Cysts |
20507500 |
Structural and functional characterization of a novel, host penetration-related pectate lyase from the potato cyst nematode Globodera rostochiensis. |
ongoing research unassigned |
3 0 |
4.2.2.2 | Cysts |
21153407 |
Molecular Variability and Evolution of the Pectate Lyase (pel-2) Parasitism Gene in Cyst Nematodes Parasitizing Different Solanaceous Plants. |
ongoing research therapeutic application unassigned |
1 1 0 |
4.2.2.2 | Cysts |
100101010 |
Structural and functional characterization of a novel, host penetration-related pectate lyase from the potato cyst nematode Globodera rostochiensis |
ongoing research unassigned |
3 0 |
4.2.2.2 | Cysts |
100101012 |
Molecular characterization and functional importance of pectate lyase secreted by the cyst nematode Heterodera schachtii |
diagnostic usage ongoing research unassigned |
3 2 0 |
4.2.2.2 | Hypersensitivity |
11325942 |
Osmoregulated periplasmic glucan synthesis is required for Erwinia chrysanthemi pathogenicity. |
causal interaction therapeutic application unassigned |
2 1 0 |
4.2.2.2 | Hypersensitivity |
16664981 |
Transient Activation of Plasmalemma K Efflux and H Influx in Tobacco by a Pectate Lyase Isozyme from Erwinia chrysanthemi. |
causal interaction unassigned |
3 0 |
4.2.2.2 | Hypersensitivity |
20458941 |
[Destabilization of defective lysogeny as the index of population dissociation of Erwinia carotovora] |
unassigned |
0 |