Species

KNApSAcK Entry

Organism name Ircinia sp.
Genus
Family
Kingdom

Metabolite list (10)

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
C00044676 External link 512 Cyclotheonamide E4
CHEMBL448961
1 / 4 / 2 No. 1491
C00044677 External link 512 Cyclotheonamide E5
CHEMBL502059
1 / 4 / 2 No. 1491
C00040044 External link 512 Polydiscamide B
No. 2212
C00040045 External link 512 Polydiscamide C
/ (+)-Polydiscamide C
CHEMBL256912
No. 2212
C00040046 External link 512 Polydiscamide D
/ (+)-Polydiscamide D
CHEMBL256131
No. 2212
C00000516 External link 512 Ircinal A
/ (+)-Ircinal A
CHEMBL332054
1 / 0 / 0 No. 2407
C00045540 External link 512 25-Hydroxy-13(24),17-cheilanthadien-16,19-olide
/ (-)-25-Hydroxy-13(24),17-cheilanthadien-16,19-olide
CHEMBL515940
2 / 0 / 0 No. 2992
C00045519 External link 512 16,25-Dihydroxy-13(24),17-cheilanthadien-19,25-olide
CHEMBL476479
2 / 0 / 0 No. 2992
C00045539 External link 512 25-Hydroxy-13(24),15,17-cheilanthatrien-18,25-olide
CHEMBL478798
2 / 0 / 0 No. 2992
C00014979 External link 512 Sch 599473
No. 4064

Human Protein / Gene in interactions

4 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75582 Ribosomal protein S6 kinase alpha-5 CAMK serine/threonine protein kinase MSKB subfamily C00045519 C00045539 C00045540 0 / 0
P49137 MAP kinase-activated protein kinase 2 CAMK serine/threonine protein kinase MAPKAPK C00045519 C00045539 C00045540 0 / 0
P00734 Prothrombin S1A C00044676 C00044677 4 / 2
P49841 Glycogen synthase kinase-3 beta Gsk C00000516 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#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 (2)

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