Species

KNApSAcK Entry

Organism name Dorstenia turbinata
Genus Dorstenia
Family Moraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Dorstenia turbinata
Linked NCBI taxonomy ID 984821
Linked level species

Family

Family in NCBI taxonomy Moraceae
ID 3487

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

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
C00007072 External link 512 Kanzonol C
/ 2',4',4-Trihydroxy-3'-prenylchalcone
CHEMBL1644933
No. 190 No. 13
C00035164 External link 512 Turbinatocoumarin
No. 399 No. 25
C00035023 External link 512 5-Methoxy-3-(3-methyl-2,3-dihydroxybutyl)psoralen
/ (-)-5-Methoxy-3-(3-methyl-2,3-dihydroxybutyl)-psoralen
No. 579 No. 25
C00029531 External link 512 Vanillic aldehyde
/ 4-Hydroxy-3-methoxybenzaldehyde
CHEMBL13883
C100058
18 / 8 / 9 33 / 1 No. 1003
C00002503 External link 512 Umbelliferon
/ Umbelliferone
/ 7-Hydroxycoumarin
CHEMBL51628
C031477
39 / 33 / 32 9 / 0 No. 1030 No. 25
C00000297 External link 512 Psoralen
CHEMBL164660
D005363
12 / 6 / 6 0 / 5 No. 1282 No. 25
C00019918 External link 512 Smyrindiol
/ Smirindiol
/ (+)-3'-Hydroxymarmesin
/ (2'S,3'R)-3'-Hydroxymarmesin
/ (+)-(2S',3'R)-3-Hydroxymarmesin
No. 1336 No. 25
C00035022 External link 512 4-Methoxyphenol
CHEMBL544
3 / 1 / 0 No. 2352

Human Protein / Gene in interactions

61 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002503 C00029531 C00035022 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002503 C00029531 2 / 2
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002503 C00029531 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000297 C00002503 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002503 C00029531 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002503 C00029531 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000297 C00002503 3 / 3
P56817 Beta-secretase 1 A1A C00000297 C00002503 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000297 C00002503 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002503 C00029531 0 / 0
Q00796 Sorbitol dehydrogenase Enzyme C00002503 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00002503 1 / 1
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00029531 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00029531 1 / 1
P00918 Carbonic anhydrase 2 Lyase C00002503 1 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00029531 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000297 0 / 1
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00029531 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00000297 0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002503 0 / 0
P28845 Corticosteroid 11-beta-dehydrogenase isozyme 1 Enzyme C00002503 1 / 1
O43570 Carbonic anhydrase 12 Lyase C00002503 1 / 2
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000297 0 / 0
P39748 Flap endonuclease 1 Enzyme C00002503 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002503 0 / 0
O75496 Geminin Unclassified protein C00002503 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00029531 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00002503 0 / 0
P18405 3-oxo-5-alpha-steroid 4-dehydrogenase 1 Oxidoreductase C00002503 0 / 0
P15121 Aldose reductase Enzyme C00002503 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00002503 0 / 0
O00519 Fatty-acid amide hydrolase 1 Enzyme C00029531 0 / 0
P29466 Caspase-1 C14 C00002503 0 / 0
P14679 Tyrosinase Oxidoreductase C00002503 4 / 2
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00029531 1 / 1
P06280 Alpha-galactosidase A Enzyme C00002503 1 / 1
Q96RI1 Bile acid receptor NR1H4 C00029531 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002503 1 / 1
Q16790 Carbonic anhydrase 9 Lyase C00002503 0 / 1
P04062 Glucosylceramidase Enzyme C00002503 6 / 4
P78527 DNA-dependent protein kinase catalytic subunit Atypical serine/threonine protein kinase PIKK subfamily C00029531 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00035022 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00002503 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002503 0 / 3
P22303 Acetylcholinesterase Hydrolase C00002503 1 / 0
P20813 Cytochrome P450 2B6 Cytochrome P450 2B6 C00000297 1 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00000297 0 / 0
P55210 Caspase-7 C14 C00002503 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000297 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000297 0 / 1
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00002503 5 / 1
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00029531 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00029531 0 / 0
P10275 Androgen receptor NR3C4 C00029531 3 / 4
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00002503 1 / 1
Q99700 Ataxin-2 Unclassified protein C00002503 1 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00002503 3 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00035022 1 / 0
O00255 Menin Unclassified protein C00002503 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002503 1 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000297 1 / 0

42 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8644 AKR1C3, DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5, PGFS, hluPGFS aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) C00002503
8574 AKR7A2, AFAR, AFAR1, AFB1-AR1, AKR7 aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) (EC:1.1.1.n11) C00002503
581 BAX, BCL2L4 BCL2-associated X protein C00002503
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002503
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00002503
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00002503
6817 SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) C00002503
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002503
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00002503
1646 AKR1C2, AKR1C-pseudo, BABP, DD, DD2, DDH2, HAKRD, HBAB, MCDR2, SRXY8 aldo-keto reductase family 1, member C2 (EC:1.3.1.20 1.1.1.357) C00029531
759 CA1, CA-I, CAB, Car1 carbonic anhydrase I (EC:4.2.1.1) C00029531
760 CA2, CA-II, CAC, CAII, Car2 carbonic anhydrase II (EC:4.2.1.1) C00029531
1196 CLK2, hCLK2 CDC-like kinase 2 (EC:2.7.12.1) C00029531
1490 CTGF, CCN2, HCS24, IGFBP8, NOV2 connective tissue growth factor C00029531
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00029531
54541 DDIT4, Dig2, REDD-1, REDD1 DNA-damage-inducible transcript 4 C00029531
1789 DNMT3B, ICF, ICF1, M.HsaIIIB DNA (cytosine-5-)-methyltransferase 3 beta (EC:2.1.1.37) C00029531
1848 DUSP6, HH19, MKP3, PYST1 dual specificity phosphatase 6 (EC:3.1.3.16 3.1.3.48) C00029531
2263 FGFR2, BBDS, BEK, BFR-1, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25 fibroblast growth factor receptor 2 (EC:2.7.10.1) C00029531
2535 FZD2, Fz2, fz-2, fzE2, hFz2 frizzled family receptor 2 C00029531
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00029531
2730 GCLM, GLCLR glutamate-cysteine ligase, modifier subunit (EC:6.3.2.2) C00029531
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00029531
3251 HPRT1, HGPRT, HPRT hypoxanthine phosphoribosyltransferase 1 (EC:2.4.2.8) C00029531
3304 HSPA1B, HSP70-1B, HSP70-2 heat shock 70kDa protein 1B C00029531
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00029531
3638 INSIG1, CL-6, CL6 insulin induced gene 1 C00029531
3727 JUND, AP-1 jun D proto-oncogene C00029531
5605 MAP2K2, CFC4, MAPKK2, MEK2, MKK2, PRKMK2 mitogen-activated protein kinase kinase 2 (EC:2.7.12.2) C00029531
57787 MARK4, MARK4L, MARK4S, MARKL1, MARKL1L, PAR-1D MAP/microtubule affinity-regulating kinase 4 (EC:2.7.11.1) C00029531
4502 MT2A, MT2 metallothionein 2A C00029531
5514 PPP1R10, CAT53, FB19, PNUTS, PP1R10, R111, p99 protein phosphatase 1, regulatory subunit 10 C00029531
11046 SLC35D2, HFRC1, SQV7L, UGTrel8, hfrc solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2 C00029531
23657 SLC7A11, CCBR1, xCT solute carrier family 7 (anionic amino acid transporter light chain, xc- system), member 11 C00029531
7041 TGFB1I1, ARA55, HIC-5, HIC5, TSC-5 transforming growth factor beta 1 induced transcript 1 C00029531
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00029531
10626 TRIM16, EBBP tripartite motif containing 16 C00029531
7360 UGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379 UDP-glucose pyrophosphorylase 2 (EC:2.7.7.9) C00029531
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00029531
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00029531
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00029531
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) C00029531

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (42)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#604931 Cortisone reductase deficiency 1; cortrd1 P28845
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#614546 Efavirenz, poor metabolism of P20813
#301500 Fabry disease P06280
#613163 Gaba-transaminase deficiency P80404
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#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
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#168600 Parkinson disease, late-onset; pd P04062
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (41)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00208 Hyperbilirubinemia P22309 (related)
H01111 Cortisone reductase deficiency (CRD) P28845 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00192 Xanthinuria P47989 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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)

Diseases related to CTD interactions

6 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008113 Liver Neoplasms C00029531
D000647 Amnesia C00000297
D002280 Carcinoma, Basal Cell C00000297
D017484 Dermatitis, Phototoxic C00000297
D056486 Drug-Induced Liver Injury C00000297
D011565 Psoriasis C00000297