| Organism name | Hypericum maculatum | 
|---|---|
| Genus | Hypericum | 
| Family | Hypericaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Hypericum maculatum | 
|---|---|
| Linked NCBI taxonomy ID | 269006 | 
| Linked level | species | 
| Family in NCBI taxonomy | Hypericaceae | 
|---|---|
| ID | 629714 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00006431   | 3,8''-Biapigenin | CHEMBL515252 | 21 / 16 / 12 | No. 34 | No. 18 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00006431 | 0 / 0 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00006431 | 0 / 0 | 
| P14618 | Pyruvate kinase PKM | Enzyme | C00006431 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00006431 | 0 / 0 | 
| P04062 | Glucosylceramidase | Enzyme | C00006431 | 6 / 4 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00006431 | 0 / 0 | 
| P54132 | Bloom syndrome protein | Enzyme | C00006431 | 1 / 2 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00006431 | 0 / 0 | 
| O75496 | Geminin | Unclassified protein | C00006431 | 0 / 0 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00006431 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00006431 | 0 / 1 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00006431 | 0 / 0 | 
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00006431 | 0 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006431 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00006431 | 4 / 3 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00006431 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00006431 | 0 / 0 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00006431 | 0 / 0 | 
| P63165 | Small ubiquitin-related modifier 1 | Unclassified protein | C00006431 | 1 / 1 | 
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00006431 | 2 / 1 | 
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00006431 | 1 / 1 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 | Q13148 | 
| #210900 | Bloom syndrome; blm | P54132 | 
| #114500 | Colorectal cancer; crc | Q14191 | 
| #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 | 
| #613705 | Orofacial cleft 10; ofc10 | P63165 | 
| #168600 | Parkinson disease, late-onset; pd | P04062 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #277700 | Werner syndrome; wrn | Q14191 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| KEGG | name | UniProt | 
|---|---|---|
| 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) | 
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) Q13148 (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00094 | DNA repair defects | P54132
                            (related) | 
| H00296 | Defects in RecQ helicases | P54132
                            (related) Q14191 (related) | 
| H00516 | Isolated orofacial clefts | P63165
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |