Species

KNApSAcK Entry

Organism name Trachelospermum asiaticum
Genus Trachelospermum
Family Apocynaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Trachelospermum asiaticum
Linked NCBI taxonomy ID 276781
Linked level species

Family

Family in NCBI taxonomy Apocynaceae
ID 4056

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (4)

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
C00000599 External link 512 (-)-Wikstromol
/ (-)-Nortrachelogenin
CHEMBL453799
CHEMBL1483370
C020436
3 / 2 / 2 No. 223 No. 21
C00000600 External link 512 (-)-Trachelogenin
CHEMBL491178
No. 223 No. 21
C00000609 External link 512 (-)-Arctigenin
CHEMBL369142
CHEMBL435734
CHEMBL1966556
C071942
13 / 7 / 6 No. 223 No. 21
C00002682 External link 512 Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid
CHEMBL120568
D014641
5 / 3 / 3 5 / 0 No. 1073

Human Protein / Gene in interactions

19 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UNA4 DNA polymerase iota Enzyme C00000609 C00002682 0 / 0
Q99700 Ataxin-2 Unclassified protein C00000599 C00000609 1 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000609 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00000599 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000609 0 / 1
P42858 Huntingtin Unclassified protein C00002682 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000609 2 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00000609 0 / 0
P15121 Aldose reductase Enzyme C00002682 0 / 0
Q02750 Dual specificity mitogen-activated protein kinase kinase 1 Ste7 C00000609 1 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00000609 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000609 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00000609 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000599 0 / 0
P03372 Estrogen receptor NR3A1 C00002682 1 / 1
P51580 Thiopurine S-methyltransferase Enzyme C00002682 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000609 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000609 0 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000609 1 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00002682
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002682
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002682
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002682
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00002682

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#615279 Cardiofaciocutaneous syndrome 3; cfc3 Q02750
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#232300 Glycogen storage disease ii P10253
#143100 Huntington disease; hd P42858
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#257220 Niemann-pick disease, type c1; npc1 O15118
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#610460 Thiopurine s-methyltransferase deficiency P51580

KEGG DISEASE (10)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00523 Noonan syndrome and related disorders Q02750 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)