| Organism name | Pieris formosa |
|---|---|
| Genus | Pieris |
| Family | Ericaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Pieris formosa |
|---|---|
| Linked NCBI taxonomy ID | 49158 |
| Linked level | species |
| Family in NCBI taxonomy | Ericaceae |
|---|---|
| ID | 4345 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | asterids |
|---|---|
| ID | 71274 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00040879
|
Asebotoxin IV
|
No. 320 | No. 45 |
|
||||
|
C00041086
|
Pierisformosin B
|
CHEMBL169864
|
No. 320 | No. 45 |
|
|||
|
C00041087
|
Pierisformosin C
/ (-)-Pierisformosin C |
No. 320 | No. 45 |
|
||||
|
C00050196
|
Pierisformosin D
/ (+)-Pierisformosin D |
No. 320 | No. 45 |
|
||||
|
C00050006
|
Asebotoxin V
|
CHEMBL1610188
|
4 / 15 / 11 | No. 320 | No. 45 |
|
||
|
C00050195
|
Pierisformoside A
/ (-)-Pierisformoside A |
No. 4673 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q16637 | Survival motor neuron protein | Unclassified protein | C00050006 | 4 / 1 |
| P02545 | Prelamin-A/C | Unclassified protein | C00050006 | 11 / 10 |
| O75496 | Geminin | Unclassified protein | C00050006 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00050006 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #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
|
| #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
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #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
|
| 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)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|