Species

KNApSAcK Entry

Organism name Tamarix aphylla
Genus Tamarix
Family Tamaricaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Tamarix aphylla
Linked NCBI taxonomy ID 189786
Linked level species

Family

Family in NCBI taxonomy Tamaricaceae
ID 63083

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

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
C00005374 External link 512 Quercetin
CHEMBL82242
CHEMBL479232
CHEMBL1437696
C012526
14 / 2 / 2 2 / 1 No. 2 No. 15
C00005591 External link 512 Tamarixin
No. 2 No. 15
C00005272 External link 512 Rhamnocitrin 3-rhamnoside
No. 2 No. 15
C00005271 External link 512 Rhamnocitrin 3-glucoside
No. 2 No. 15
C00004967 External link 512 Rhamnetin 3,5,4'-tri-O-sulfate
No. 51 No. 15
C00004951 External link 512 Kaempferol 7,4'-dimethyl ether 3-O-sulfate
No. 51 No. 15
C00002752 External link 512 Isoferulic acid
CHEMBL233295
C008180
5 / 9 / 6 0 / 1 No. 1366 No. 6
C00006071 External link 512 Rhamnetin 3'-glucuronide-3,5,4'-trisulfate
No. 3733
C00034881 External link 512 N-Methyl-L-proline
/ (-)-N-Methyl-L-proline
No. 5329
C00034907 External link 512 trans-4-Hydroxy-N-methyl-L-proline
/ (-)-trans-4-Hydroxy-N-methyl-L-proline
No. 5329

Human Protein / Gene in interactions

19 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9P1W9 Serine/threonine-protein kinase pim-2 Pim C00005374 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00005374 1 / 1
P07237 Protein disulfide-isomerase Enzyme C00005374 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00005374 0 / 0
P39748 Flap endonuclease 1 Enzyme C00005374 0 / 0
P15121 Aldose reductase Enzyme C00005374 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002752 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00005374 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00005374 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002752 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002752 0 / 0
P03372 Estrogen receptor NR3A1 C00002752 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00005374 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00005374 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005374 0 / 0
Q12794 Hyaluronidase-1 Enzyme C00002752 1 / 2
Q9UBT6 DNA polymerase kappa Enzyme C00005374 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00005374 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00005374 0 / 0

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00005374
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00005374

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#615363 Estrogen resistance; estrr P03372
#174800 Mccune-albright syndrome; mas P63092
#601492 Mucopolysaccharidosis, type ix; mps9 Q12794
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (8)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00192 Xanthinuria P47989 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00133 Mucopolysaccharidosis type IX (MPS9) Q12794 (related)
H00421 Mucopolysaccharidosis (MPS) Q12794 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00002752
D010146 Pain C00005374