Species

KNApSAcK Entry

Organism name Retama sphaerocarpa
Genus Retama
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Retama sphaerocarpa
Linked NCBI taxonomy ID 49838
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

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
C00013934 External link 512 Rhamnazin 3-glucosyl-(1->5)-alpha-L-arabinofuranoside
/ Quercetin 7,3'-dimethyl ether 3-glucosyl-(1->5)-alpha-L-arabinofuranoside
/ 3-[(5-O-beta-D-Glucopyranosyl-alpha-L-arabinofuranosyl)oxy]-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
No. 1 No. 15
C00002518 External link 512 Daidzin
/ Daidzoside
/ Daidzein 7-O-glucoside
CHEMBL486422
C013908
11 / 18 / 41 3 / 2 No. 2 No. 15
C00002528 External link 512 Genistin
/ Genistoside
/ Genistein 7-O-glucoside
/ Genistein 7-O-beta-glucopyranoside
CHEMBL486625
CHEMBL1364260
C040641
15 / 32 / 53 6 / 2 No. 2 No. 15
C00010097 External link 512 Fujikinetin 7-O-glucoside
/ 7-Hydroxy-6'-methoxy-3',4'-methylenedioxyisoflavone 7-O-glucoside
No. 2 No. 15
C00013936 External link 512 Retamatrioside
/ Rhamnazin 3-glucosyl-(1->5)-[apiosyl-(1->2)-alpha-L-arabinofuranoside]
/ Quercetin 7,3'-dimethyl ether 3-glucosyl-(1->5)-[apiosyl-(1->2)-alpha-L-arabinofuranoside]
/ 3-[[O-D-apio-beta-D-furanosyl-(1->2)-O-[beta-D-glucopyranosyl-(1->5)]-alpha-L-arabinofuranosyl]oxy]-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
No. 5 No. 15
C00002225 External link 512 Lupanine
/ (+)-Lupanine
CHEMBL459396
CHEMBL520093
CHEMBL2008918
C008298
No. 85 No. 3
C00002014 External link 512 (+)-Ammodendrine
/ (+)-Spherocarpine
CHEMBL464776
CHEMBL464777
C068578
No. 2560 No. 1

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00002518 C00002528 7 / 37
Q16637 Survival motor neuron protein Unclassified protein C00002518 C00002528 4 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002518 C00002528 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002518 C00002528 1 / 1
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002518 C00002528 4 / 2
P51151 Ras-related protein Rab-9A Unclassified protein C00002518 C00002528 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002518 0 / 0
O75496 Geminin Unclassified protein C00002528 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002528 1 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00002518 1 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002528 1 / 8
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002528 2 / 2
P02545 Prelamin-A/C Unclassified protein C00002528 11 / 10
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002528 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002528 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002518 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002528 1 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002518 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002518 1 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002528 1 / 1

9 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
217 ALDH2, ALDH-E2, ALDHI, ALDM aldehyde dehydrogenase 2 family (mitochondrial) (EC:1.2.1.3) C00002518
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00002518
5241 PGR, NR3C3, PR progesterone receptor C00002518
2539 G6PD, G6PD1 glucose-6-phosphate dehydrogenase (EC:1.1.1.49) C00002528
4489 MT1A, MT1, MT1S, MTC metallothionein 1A C00002528
4493 MT1E, MT1, MTD metallothionein 1E C00002528
4501 MT1X, MT-1l, MT1 metallothionein 1X C00002528
4502 MT2A, MT2 metallothionein 2A C00002528
7779 SLC30A1, ZNT1, ZRC1 solute carrier family 30 (zinc transporter), member 1 C00002528

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (34)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#610251 Alcohol sensitivity, acute P05091
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#211980 Lung cancer P00533
P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257220 Niemann-pick disease, type c1; npc1 O15118
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#275210 Restrictive dermopathy, lethal P02545
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#275355 Squamous cell carcinoma, head and neck; hnscc P04637

KEGG DISEASE (55)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
H00018 Gastric cancer P00533 (related)
P04637 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P04637 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H01071 Acute alcohol sensitivity P05091 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00548 Brunner syndrome P21397 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D011471 Prostatic Neoplasms C00002518
C00002528
D008569 Memory Disorders C00002518
D005831 Genital Diseases, Female C00002528