| Organism name | Boesenbergia rotunda (L.) Mansf.Kulturpfl. |
|---|---|
| Genus | Boesenbergia |
| Family | Zingiberaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Boesenbergia |
|---|---|
| Linked NCBI taxonomy ID | 97724 |
| Linked level | genus |
| Family in NCBI taxonomy | Zingiberaceae |
|---|---|
| ID | 4642 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | Liliopsida |
|---|---|
| ID | 4447 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00000999
|
Sakuranetin
/ Naringenin 7-O-methyl ether / 5,4'-Dihydroxy-7-methoxyflavanone |
CHEMBL74852
CHEMBL448297 |
C099724
|
19 / 20 / 20 | No. 25 | No. 14 |
|
|
|
C00036493
|
2'-Hydroxy-4,4',6'-trimethoxychalcone
|
CHEMBL243829
|
3 / 3 / 0 | No. 79 |
|
|||
|
C00006934
|
Pinostrobin chalcone
/ 2',6'-Dihydroxy-4'-methoxychalcone |
CHEMBL317221
CHEMBL1705800 |
3 / 1 / 2 | No. 92 | No. 13 |
|
||
|
C00007131
|
Boesenbergin A
|
CHEMBL442440
|
No. 186 |
|
||||
|
C00003444
|
miropinic acid
/ Isopimaric acid / isodextropimaric acid |
CHEMBL512164
|
C115138
|
3 / 1 / 1 | No. 208 | No. 48 |
|
|
|
C00036322
|
(+)-Zeylenol
|
No. 2680 |
|
|||||
|
C00036823
|
Boesenboxide
/ (+)-Boesenboxide |
No. 3545 |
|
|||||
|
C00036940
|
Crotepoxide
/ (+)-Crotepoxide |
CHEMBL1976475
|
C011828
|
No. 3545 |
|
|||
|
C00007133
|
Rubranine
|
No. 4362 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P33527 | Multidrug resistance-associated protein 1 | drugs | C00036493 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00000999 | 1 / 1 |
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00000999 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00000999 | 6 / 4 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00000999 | 0 / 0 |
| Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00000999 | 1 / 4 |
| P08183 | Multidrug resistance protein 1 | drug | C00036493 | 1 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00006934 | 0 / 1 |
| P47870 | Gamma-aminobutyric acid receptor subunit beta-2 | GABA-A beta | C00003444 | 0 / 0 |
| P14867 | Gamma-aminobutyric acid receptor subunit alpha-1 | GABA-A alpha | C00003444 | 1 / 1 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00000999 | 2 / 3 |
| Q9Y3R4 | Sialidase-2 | Enzyme | C00000999 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00000999 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00003444 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000999 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00000999 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00000999 | 1 / 1 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00000999 | 0 / 0 |
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00036493 | 2 / 0 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00000999 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00006934 | 1 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006934 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00000999 | 4 / 3 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00000999 | 1 / 1 |
| P59538 | Taste receptor type 2 member 31 | Taste receptor (taste family GPCR) | C00000999 | 0 / 0 |
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00000999 | 0 / 1 |
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00000999 | 1 / 4 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00000999 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #208900 | Ataxia-telangiectasia; at |
Q13315
|
| #614490 | Blood group, junior system; jr |
Q9UNQ0
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #611136 | Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 |
P14867
|
| #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
|
| #612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| #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)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00342 | Tuberculosis |
P11473
(related)
|
| H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
| H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00808 | Idiopathic generalized epilepsies (IGEs) |
P14867
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
| H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
| H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
| H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
| H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
| H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
| H00094 | DNA repair defects |
Q13315
(related)
|
| H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|