Species

KNApSAcK Entry

Organism name Oscillatoria agardhii
Genus
Family
Kingdom

NCBI taxonomy

Entry

Linked NCBI taxonomy name Planktothrix agardhii
Linked NCBI taxonomy ID 1160
Linked level species

Family

Family in NCBI taxonomy
ID

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Bacteria
ID 2

Plant class

Plant class
ID

Metabolite list (11)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00027847 External link 512 Anabaenopeptin H
CHEMBL22281
CHEMBL502149
1 / 0 / 0 No. 445
C00028778 External link 512 Oscillamide Y
CHEMBL446236
2 / 0 / 0 No. 445
C00028777 External link 512 Oscillamide H
No. 445
C00027845 External link 512 Anabaenopeptin F
CHEMBL175436
3 / 0 / 0 No. 445
C00027846 External link 512 Anabaenopeptin G
No. 445
C00028859 External link 512 Prenylagaramide B
No. 498
C00003779 External link 512 Mutatochrome
/ beta-carotene 5,8-epoxide
C001792
No. 1206 No. 59
C00028858 External link 512 Prenylagaramide A
CHEMBL507696
3 / 5 / 3 No. 2259
C00027813 External link 512 Aeruginosin 205B
No. 4473
C00027812 External link 512 Aeruginosin 205A
No. 4473
C00028474 External link 512 Lipopurealin A
CHEMBL206373
No. 8538

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P30305 M-phase inducer phosphatase 2 Ser_Thr_Tyr C00027845 C00028778 0 / 0
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00027845 C00028778 0 / 0
P15085 Carboxypeptidase A1 M14A C00027845 C00027847 0 / 0
P00734 Prothrombin S1A C00028858 4 / 2
P28838 Cytosol aminopeptidase M17 C00028858 0 / 0
P00747 Plasminogen S1A C00028858 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#217090 Plasminogen deficiency, type i P00747
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (3)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
P00747 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H01206 Plasminogen deficiency P00747 (related)