Plant Species


Cumulative plant class count

class name count
rosids 3

Cumulative family count

class name count
Brassicaceae 3
Mactridae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (4)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00007540 External link 512 Sphinganine
CHEMBL448741
CHEMBL1442934
CHEMBL1487948
C005682
41 / 51 / 73 0 / 1
C00007541 External link 512 Sphinganine-1-phosphate
CHEMBL78539
CHEMBL78494
CHEMBL311863
3 / 0 / 0
C00007543 External link 512 4-Hydroxysphinganine
CHEMBL236036
CHEMBL466395
2 / 2 / 3
C00044752 External link 512 ES-285
/ Spisulosine 285
CHEMBL1835439

Human Protein / Gene in interactions

44 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P11473 Vitamin D3 receptor NR1I1 C00007540 C00007543 2 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00007540 C00007543 0 / 0
O75496 Geminin Unclassified protein C00007540 0 / 0
Q99700 Ataxin-2 Unclassified protein C00007540 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00007540 2 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00007540 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00007540 2 / 2
P06746 DNA polymerase beta Enzyme C00007540 0 / 0
P04062 Glucosylceramidase Enzyme C00007540 6 / 4
O95136 Sphingosine 1-phosphate receptor 2 EDG receptor C00007541 0 / 0
P02545 Prelamin-A/C Unclassified protein C00007540 11 / 10
P11597 Cholesteryl ester transfer protein Secreted protein C00007540 1 / 1
P08183 Multidrug resistance protein 1 drug C00007540 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00007540 0 / 1
P54132 Bloom syndrome protein Enzyme C00007540 1 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00007540 1 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00007540 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00007540 2 / 2
P21453 Sphingosine 1-phosphate receptor 1 EDG receptor C00007541 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00007540 0 / 0
P42858 Huntingtin Unclassified protein C00007540 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007540 2 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00007540 7 / 37
Q9Y253 DNA polymerase eta Enzyme C00007540 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00007540 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00007540 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00007540 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00007540 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00007540 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00007540 0 / 1
P61088 Ubiquitin-conjugating enzyme E2 N Enzyme C00007540 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00007540 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00007540 4 / 3
Q99549 M-phase phosphoprotein 8 Unclassified protein C00007540 0 / 0
Q99500 Sphingosine 1-phosphate receptor 3 EDG receptor C00007541 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00007540 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00007540 0 / 0
P40225 Thrombopoietin Unclassified protein C00007540 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00007540 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00007540 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00007540 1 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00007540 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00007540 1 / 4
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007540 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (51)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#210900 Bloom syndrome; blm P54132
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#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
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#143470 Hyperalphalipoproteinemia 1; halp1 P11597
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer 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
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#609620 Short qt syndrome 1; sqt1 Q12809
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (73)

KEGG name UniProt
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)
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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (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)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01199 Hyperalphalipoproteinemia P11597 (related)
H01205 Coumarin resistance P11712 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00059 Huntington's disease (HD) P42858 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00007540