Species

KNApSAcK Entry

Organism name Gnetum cleistostachyum
Genus Gnetum
Family Gnetaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Gnetum
Linked NCBI taxonomy ID 3380
Linked level genus

Family

Family in NCBI taxonomy Gnetaceae
ID 3379

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

Metabolite list (8)

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
C00031370 External link 512 Shegansu B
/ Parvifolol D
/ (+)-Shegansu
/ (+)-Parvifolol D
No. 108 No. 30
C00015784 External link 512 Gnetol
No. 295 No. 13
C00019308 External link 512 Doursterol
/ Daucosterin
/ 3-O-beta-D-Glucopyranosyl sitosterol
/ beta-Sitosterol 3-O-beta-D-glucopyranoside
CHEMBL197711
CHEMBL506678
CHEMBL2304043
C011015
5 / 4 / 2 0 / 3 No. 520
C00030413 External link 512 Gnetofuran A
No. 2166
C00030650 External link 512 Lehmbachol D
/ (+)-Lehmbachol D
No. 3074
C00015773 External link 512 Gnetifolin F
No. 3074
C00030415 External link 512 Gnetupendin B
No. 3340
C00030414 External link 512 Gnetumontanin C
No. 5068

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00019308 0 / 0
P06746 DNA polymerase beta Enzyme C00019308 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00019308 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00019308 0 / 0
P00734 Prothrombin S1A C00019308 4 / 2

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)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002493 Central Nervous System Diseases C00019308
D003072 Cognition Disorders C00019308
D013118 Spinal Cord Diseases C00019308