Organism name | Machilus japonica |
---|---|
Genus | Machilus |
Family | Lauraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Persea japonica |
---|---|
Linked NCBI taxonomy ID | 325535 |
Linked level | species |
Family in NCBI taxonomy | Lauraceae |
---|---|
ID | 3433 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Magnoliophyta |
---|---|
ID | 3398 |
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 |
---|---|---|---|---|---|---|---|---|
C00000697
![]() |
(-)-Machilusin
|
CHEMBL471177
CHEMBL469499 CHEMBL559937 |
No. 38 | No. 21 |
![]() |
|||
C00002611
![]() |
Licarin A
/ (-)-Licarin A |
CHEMBL259731
CHEMBL463526 CHEMBL1732407 |
9 / 7 / 3 | No. 215 | No. 23 |
![]() |
||
C00047850
![]() |
dl-Coclaurine
|
CHEMBL256448
CHEMBL453291 CHEMBL446211 |
8 / 17 / 10 | No. 253 | No. 4 |
![]() |
||
C00007213
![]() |
(-)-Galbacin
|
CHEMBL1980140
CHEMBL2151191 |
2 / 0 / 0 | No. 621 | No. 21 |
![]() |
||
C00002605
![]() |
(+)-Galbacin
|
CHEMBL1980140
CHEMBL2151191 |
2 / 0 / 0 | No. 621 | No. 21 |
![]() |
||
C00047722
![]() |
Apigenosylide B
/ (+)-Apigenosylide B |
CHEMBL538176
|
No. 4037 |
![]() |
||||
C00047723
![]() |
Apigenosylide C
/ (-)-Apigenosylide C |
CHEMBL558750
|
No. 4037 |
![]() |
||||
C00047721
![]() |
Apigenosylide A
/ (+)-Apigenosylide A |
CHEMBL540481
|
No. 4037 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16539 | Mitogen-activated protein kinase 14 | p38 | C00002605 C00007213 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002611 C00047850 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00002611 C00047850 | 0 / 0 |
P45984 | Mitogen-activated protein kinase 9 | Jnk | C00002605 C00007213 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00002611 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00002611 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002611 | 2 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00047850 | 6 / 4 |
P37840 | Alpha-synuclein | Unclassified protein | C00002611 | 4 / 2 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00047850 | 7 / 3 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002611 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002611 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00047850 | 4 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00047850 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00047850 | 0 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | C00047850 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002611 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#114500 | Colorectal cancer; crc |
P84022
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#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
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P04062
P37840 |
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
P37840 (related) |
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|