Macroptilium atropurpureum
Species
KNApSAcK Entry
| Organism name | Macroptilium atropurpureum |
|---|---|
| Genus | Macroptilium |
| Family | Fabaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Macroptilium atropurpureum |
|---|---|
| Linked NCBI taxonomy ID | 90550 |
| 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 (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 |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
C00020271
|
alpha-Rhamnorobin
/ Kaempferol 7-O-alpha-L-rhamnofuranoside |
No. 2 | No. 15 |
|
||||
|
C00002520
|
Dalbergioidin
/ 5,7,2',4'-Tetrahydroxyisoflavanone |
No. 106 | No. 14 |
|
||||
|
C00001164
|
Myoinositol
/ myo-Inositol |
CHEMBL278373
CHEMBL468154 CHEMBL1222251 CHEMBL1231671 CHEMBL1950780 |
8 / 17 / 18 | No. 795 |
|
|||
|
C00001555
|
Trigonelline
|
CHEMBL350675
|
C009560
|
3 / 1 / 0 | No. 3681 | No. 1 |
|
Human Protein / Gene in interactions
11 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10323 | Acrosin | S1A | C00001164 | 0 / 0 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00001555 | 0 / 0 |
| P02545 | Prelamin-A/C | Unclassified protein | C00001164 | 11 / 10 |
| P16278 | Beta-galactosidase | Enzyme | C00001164 | 4 / 6 |
| O75496 | Geminin | Unclassified protein | C00001164 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001555 | 0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00001164 | 1 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001164 | 0 / 0 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00001164 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001555 | 1 / 0 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00001164 | 1 / 1 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (18)
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #301500 | Fabry disease |
P06280
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #230500 | Gm1-gangliosidosis, type i |
P16278
|
| #230600 | Gm1-gangliosidosis, type ii |
P16278
|
| #230650 | Gm1-gangliosidosis, type iii |
P16278
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #253010 | Mucopolysaccharidosis type ivb |
P16278
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
KEGG DISEASE (18)
| 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)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
| H00276 | Galactosialidosis |
P16278
(related)
|
| H00281 | GM1 gangliosidosis |
P16278
(related)
|
| H00421 | Mucopolysaccharidosis (MPS) |
P16278
(related)
|
| H00422 | Glycoproteinoses |
P16278
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P16278
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|