Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Aglajidae 4

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (7)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00028434 External link 512 Kulokainalide-1
C00028435 External link 512 Kulolide 1
C00028436 External link 512 Kulolide-2
C00028437 External link 512 Kulolide-3
C00034529 External link 512 Guineamide E
/ (-)-Guineamide E
C00034638 External link 512 Pitipeptolide A
/ (-)-Pitipeptolide A
CHEMBL505780
CHEMBL1889891
6 / 9 / 4
C00034639 External link 512 Pitipeptolide B
CHEMBL505027
CHEMBL1902777
6 / 9 / 4

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00034638 C00034639 1 / 1
P00747 Plasminogen S1A C00034638 C00034639 1 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00034638 C00034639 2 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00034638 C00034639 0 / 0
P00734 Prothrombin S1A C00034638 C00034639 4 / 2
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00034638 C00034639 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#137800 Glioma susceptibility 1; glm1 O75874
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#217090 Plasminogen deficiency, type i P00747
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (4)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
P00747 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H01206 Plasminogen deficiency P00747 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)