PCIDB

Teclea gerrardii

Species

KNApSAcK Entry

Organism name Teclea gerrardii
Genus Teclea
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Teclea gerrardii
Linked NCBI taxonomy ID 1237830
Linked level species

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

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 		KCF-S
cluster 		phytochemical
cluster 		figure
C00002137 External link 512 Arborinine
CHEMBL349609
C022784
1 / 0 / 0 No. 257 No. 7
C00034720 External link 512 Tegerrardin A
CHEMBL1095073
No. 257 No. 7
C00024251 External link 512 Evoxanthine
No. 257 No. 7
C00034360 External link 512 1,3-Dimethoxy-N-methylacridone
No. 257 No. 7
C00034721 External link 512 Tegerrardin B
No. 469 No. 7
C00002158 External link 512 Evoxine
/ 7-(2,3-Dihydroxy-3-methyl-butyl)oxy-8-methyldictamnine
CHEMBL1317300
CHEMBL1395597
CHEMBL1416006
14 / 9 / 9 No. 600 No. 7
C00034719 External link 512 Tecleanone
No. 6039

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002158 1 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00002137 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002158 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002158 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002158 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002158 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002158 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002158 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002158 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002158 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002158 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002158 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002158 0 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002158 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002158 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714

KEGG DISEASE (9)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)