Species

KNApSAcK Entry

Organism name Citrullus colocynthis (L.)
Genus Citrullus
Family Cucurbitaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Citrullus
Linked NCBI taxonomy ID 3653
Linked level genus

Family

Family in NCBI taxonomy Cucurbitaceae
ID 3650

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (14)

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
C00001059 External link 512 Isovitexin
/ Saponaretin
/ Homovitexin
/ 6-C-beta-D-Glucopyranosylapigenin
/ 6-beta-D-Glucopyranosyl-4',5,7-trihydroxyflavone
/ 6-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
CHEMBL465360
CHEMBL1601394
C049772
28 / 20 / 19 No. 22 No. 15
C00030466 External link 512 Helicid
/ 4-(beta-D-glucopyranosyloxy) benzaldehyde
CHEMBL201358
CHEMBL461515
C055677
2 / 2 / 2 No. 45 No. 72
C00029534 External link 512 4-Hydroxybenzyl beta-D-glucopyranoside
No. 45 No. 72
C00029516 External link 512 Gastrodin
/ (-)-Gastrodin
/ 4-(beta-D-Glucopyranosyloxy) benzyl alcohol
CHEMBL274739
C045345
2 / 2 / 2 0 / 2 No. 45 No. 72
C00029812 External link 512 Benzyl beta-D-glucopyranoside
/ (-)-Benzyl-O-beta-D-glucopyranoside
CHEMBL1170453
CHEMBL2336738
C410942
No. 45 No. 72
C00030034 External link 512 Cucurbitacin l 2-O-beta-D-glucopyranoside
CHEMBL449483
1 / 4 / 2 No. 315
C00030001 External link 512 Colocynthoside A
/ (-)-Colocynthoside A
No. 315
C00030032 External link 512 Cucurbitacin K 2-O-beta-glucopyranoside
/ Cucurbitacin K 2-O-beta-D-glucopyranoside
CHEMBL1923785
CHEMBL1923786
No. 315
C00030029 External link 512 Elaterinide
/ Gratiotoxin
/ Cucurbitacin E-2-O-glucoside
/ alpha-Elaterin 2-D-glucopyranoside
/ Cucurbitacin E 2-O-beta-D-glucopyranoside
CHEMBL1455367
CHEMBL1765381
8 / 5 / 3 No. 315
C00030031 External link 512 Cucurbitacin I 2-O-beta-D-glucopyranoside
CHEMBL1723294
CHEMBL1765380
2 / 0 / 0 No. 315
C00030608 External link 512 Khekadaengoside E
/ (-)-Khekadaengoside E
No. 315
C00030002 External link 512 Colocynthoside B
/ (-)-Colocynthoside B
No. 675 No. 51
C00029478 External link 512 3,4'-Dihydroxypropiophenone
/ 4-Hydroxy-(3-hydroxypropionyl)benzene
CHEMBL1417159
25 / 10 / 7 No. 2849
C00029477 External link 512 beta-Hydroxypropiovanillone
/ omega-Hydroxypropioguaiacone
/ 3,4'-Dihydroxy-3'-methoxypropiophenone
/ 3-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-1-propanone
CHEMBL485875
No. 2959

Human Protein / Gene in interactions

42 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001059 C00030029 C00030031 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001059 C00029478 C00030029 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001059 C00029478 C00030029 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001059 C00029478 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00001059 C00029478 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001059 C00029478 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00029516 C00030466 1 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001059 C00029478 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001059 C00029478 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001059 C00029478 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001059 C00030029 1 / 0
P06746 DNA polymerase beta Enzyme C00001059 C00029478 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001059 C00029478 1 / 1
P46063 ATP-dependent DNA helicase Q1 Enzyme C00001059 C00029478 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001059 C00029478 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00001059 C00029478 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00001059 C00029478 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001059 C00029478 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00001059 C00029478 2 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00029478 C00030031 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00001059 C00029478 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001059 C00029478 0 / 0
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00029516 C00030466 1 / 1
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00029478 0 / 0
P30989 Neurotensin receptor type 1 Neurotensin receptor C00001059 0 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00029478 0 / 1
P14679 Tyrosinase Oxidoreductase C00030034 4 / 2
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00029478 3 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00001059 0 / 0
P09923 Intestinal-type alkaline phosphatase Enzyme C00029478 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00001059 7 / 3
O75496 Geminin Unclassified protein C00030029 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00029478 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00030029 2 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00001059 2 / 2
O00255 Menin Unclassified protein C00001059 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001059 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00001059 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001059 1 / 4
P54132 Bloom syndrome protein Enzyme C00029478 1 / 2
Q99700 Ataxin-2 Unclassified protein C00030029 1 / 1
Q06710 Paired box protein Pax-8 Unclassified protein C00030029 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (33)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#210900 Bloom syndrome; blm P54132
#114500 Colorectal cancer; crc P84022
Q14191
#613163 Gaba-transaminase deficiency P80404
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#218700 Hypothyroidism, congenital, nongoitrous, 2; chng2 Q06710
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (28)

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)
H00213 Hypophosphatasia P05186 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00023 Testicular cancer P10696 (marker)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00032 Thyroid cancer Q06710 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) Q06710 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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 C00029516
D007859 Learning Disorders C00029516