| Organism name | Lonchocarpus sericeus |
|---|---|
| Genus | Lonchocarpus |
| Family | Fabaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Lonchocarpus sericeus |
|---|---|
| Linked NCBI taxonomy ID | 1225672 |
| Linked level | species |
| Family in NCBI taxonomy | Fabaceae |
|---|---|
| ID | 3803 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00008686
|
Fustin 3-glucoside
|
No. 12 | No. 14 |
|
||||
|
C00008132
|
(-)-Isolonchocarpin
|
No. 127 | No. 14 |
|
||||
|
C00007045
|
Isocordoin
|
CHEMBL460618
|
No. 133 | No. 13 |
|
|||
|
C00007049
|
Flemistrictin B
|
No. 337 |
|
|||||
|
C00002037
|
DMDP
/ (+)-2,5-Dideoxy-2,5-imino-D-mannitol / 2R,5R-Dihydroxymethyl-3R,4R-dihydroxy-pyrrolidine |
CHEMBL10437
CHEMBL312653 CHEMBL121093 CHEMBL259905 CHEMBL405957 CHEMBL469844 CHEMBL2008021 |
C043121
|
8 / 10 / 8 | No. 667 |
|
||
|
C00002035
|
1-Deoxymannojirimycin
/ (-)-Deoxymannojirimycin |
CHEMBL11510
CHEMBL65131 CHEMBL307429 CHEMBL84844 CHEMBL110458 CHEMBL369297 CHEMBL179085 CHEMBL176206 CHEMBL179130 CHEMBL179347 CHEMBL179409 CHEMBL176021 CHEMBL369046 CHEMBL176209 CHEMBL368121 CHEMBL175901 CHEMBL1337303 |
33 / 27 / 27 | No. 786 | No. 1 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00002035 C00002037 | 6 / 4 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00002035 C00002037 | 0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00002035 C00002037 | 1 / 1 |
| Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00002035 C00002037 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002035 C00002037 | 1 / 1 |
| Q9H227 | Cytosolic beta-glucosidase | Enzyme | C00002035 C00002037 | 0 / 0 |
| P35573 | Glycogen debranching enzyme | Enzyme | C00002035 C00002037 | 1 / 1 |
| P04066 | Tissue alpha-L-fucosidase | Enzyme | C00002035 C00002037 | 1 / 2 |
| O00462 | Beta-mannosidase | Enzyme | C00002035 | 1 / 2 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00002035 | 3 / 1 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002035 | 0 / 1 |
| P23458 | Tyrosine-protein kinase JAK1 | Jakb | C00002035 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00002035 | 0 / 0 |
| P14410 | Sucrase-isomaltase, intestinal | Enzyme | C00002035 | 1 / 1 |
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002035 | 1 / 0 |
| Q13133 | Oxysterols receptor LXR-alpha | NR1H3 | C00002035 | 0 / 0 |
| P16278 | Beta-galactosidase | Enzyme | C00002035 | 4 / 6 |
| Q9HCG7 | Non-lysosomal glucosylceramidase | Enzyme | C00002035 | 1 / 0 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002035 | 0 / 0 |
| P55055 | Oxysterols receptor LXR-beta | NR1H3 | C00002035 | 0 / 0 |
| P09848 | Lactase-phlorizin hydrolase | Enzyme | C00002035 | 1 / 1 |
| Q16739 | Ceramide glucosyltransferase | Transferase | C00002035 | 0 / 0 |
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002035 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002035 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002035 | 0 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002035 | 0 / 0 |
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00002035 | 0 / 0 |
| O43280 | Trehalase | Enzyme | C00002035 | 0 / 0 |
| O00754 | Lysosomal alpha-mannosidase | Enzyme | C00002035 | 1 / 2 |
| Q6P4F1 | Alpha-(1,3)-fucosyltransferase 10 | Enzyme | C00002035 | 0 / 0 |
| Q9Y2E5 | Epididymis-specific alpha-mannosidase | Enzyme | C00002035 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00002035 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002035 | 1 / 2 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #301500 | Fabry disease |
P06280
|
| #230000 | Fucosidosis |
P04066
|
| #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
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #232400 | Glycogen storage disease iii |
P35573
|
| #230500 | Gm1-gangliosidosis, type i |
P16278
|
| #230600 | Gm1-gangliosidosis, type ii |
P16278
|
| #230650 | Gm1-gangliosidosis, type iii |
P16278
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #223000 | Lactase deficiency, congenital |
P09848
|
| #248500 | Mannosidosis, alpha b, lysosomal; mansa |
O00754
|
| #248510 | Mannosidosis, beta a, lysosomal; mansb |
O00462
|
| #253010 | Mucopolysaccharidosis type ivb |
P16278
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #614409 | Spastic paraplegia 46, autosomal recessive; spg46 |
Q9HCG7
|
| #222900 | Sucrase-isomaltase deficiency, congenital; csid |
P14410
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
| 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)
|
| H00140 | beta-Mannosidosis |
O00462
(related)
|
| H00422 | Glycoproteinoses |
O00462
(related)
O00754 (related) P04066 (related) P16278 (related) |
| H00139 | alpha-Mannosidosis |
O00754
(related)
|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
P16278 (related) |
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00141 | Fucosidosis |
P04066
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00116 | Congenital lactase deficiency |
P09848
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
P35573 (related) |
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|
| H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
| H00276 | Galactosialidosis |
P16278
(related)
|
| H00281 | GM1 gangliosidosis |
P16278
(related)
|
| H00421 | Mucopolysaccharidosis (MPS) |
P16278
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(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)
|