Organism name | Neoraputia paraensis |
---|---|
Genus | Neoraputia |
Family | Rutaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Rutaceae |
---|---|
Linked NCBI taxonomy ID | 23513 |
Linked level | family |
Family in NCBI taxonomy | Rutaceae |
---|---|
ID | 23513 |
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 |
---|---|---|---|---|---|---|---|---|
C00004082
![]() |
5,6,7,3',4',5'-Hexamethoxyflavone
/ 5,6,7-Trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL370963
|
1 / 1 / 0 | No. 8 | No. 15 |
![]() |
||
C00003918
![]() |
5,7,3',4',5'-Pentamethoxyflavone
/ Tricetin 5,7,3',4',5'-pentamethyl ether / 5,7-Dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL2074901
|
1 / 1 / 0 | No. 8 | No. 15 |
![]() |
||
C00003946
![]() |
5,4'-Dihidroxy-6,7,3',5'-tetramethoxyflavone
/ 5-Hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-dimethoxy-4H-1-benzopyran-4-one |
CHEMBL1524286
|
16 / 10 / 6 | No. 8 | No. 15 |
![]() |
||
C00013440
![]() |
5-Hydroxy-8-(4-hydroxy-3,5-dimethoxyphenyl)-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b']dipyran-6-one
|
No. 24 | No. 15 |
![]() |
||||
C00004006
![]() |
5,6,7,3'-Tetramethoxy-4',5'-methylenedioxyflavone
|
No. 27 | No. 15 |
![]() |
||||
C00013402
![]() |
Ageconyflavone A
/ 3',4'-Methylenedioxy-5,6,7-trimethoxyflavone / 2-(1,3-Benzodioxol-5-yl)-5,6,7-trimethoxy-4H-1-benzopyran-4-one |
No. 27 | No. 15 |
![]() |
||||
C00002161
![]() |
Flindersiamine
/ 8-Methoxy-6,7-methylenedioxydictamnine |
CHEMBL503519
|
C012321
|
No. 368 | No. 7 |
![]() |
||
C00026399
![]() |
8-O-Tigloyldiderroside
|
No. 799 | No. 7 |
![]() |
||||
C00013441
![]() |
5-Hydroxy-8-(4-hydroxy-3,5-dimethoxyphenyl)-10-methoxy-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b']dipyran-6-one
|
No. 1516 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P08183 | Multidrug resistance protein 1 | drug | C00003918 C00004082 | 1 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00003946 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00003946 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00003946 | 1 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00003946 | 1 / 0 |
P50281 | Matrix metalloproteinase-14 | M10A | C00003946 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00003946 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003946 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00003946 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00003946 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003946 | 4 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00003946 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00003946 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00003946 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003946 | 1 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00003946 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00003946 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#114500 | Colorectal cancer; crc |
Q14191
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|