| 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)
|