Organism name | Piper hispidum |
---|---|
Genus | Piper |
Family | Piperaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Piper hispidum |
---|---|
Linked NCBI taxonomy ID | 130401 |
Linked level | species |
Family in NCBI taxonomy | Piperaceae |
---|---|
ID | 16739 |
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 |
---|---|---|---|---|---|---|---|---|
C00008158
![]() |
5,7,8-Trimethoxyflavanone
|
No. 25 | No. 14 |
![]() |
||||
C00008155
![]() |
8-Hydroxy-5,7-dimethoxyflavanone
|
CHEMBL1350188
|
21 / 16 / 18 | No. 25 | No. 14 |
![]() |
||
C00008150
![]() |
6-Hydroxy-5,7-dimethoxyflavanone
|
No. 25 | No. 14 |
![]() |
||||
C00006961
![]() |
2',3'-Dihydroxy-4',6'-dimethoxychalcone
|
CHEMBL1446527
|
13 / 17 / 11 | No. 79 |
![]() |
|||
C00006963
![]() |
2'-Hydroxy-3',4',6'-trimethoxychalcone
|
No. 79 |
![]() |
|||||
C00006935
![]() |
Cardamomin
|
CHEMBL378104
|
13 / 18 / 14 | No. 92 | No. 13 |
![]() |
||
C00006934
![]() |
Pinostrobin chalcone
/ 2',6'-Dihydroxy-4'-methoxychalcone |
CHEMBL317221
CHEMBL1705800 |
3 / 1 / 2 | No. 92 | No. 13 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
O75164 | Lysine-specific demethylase 4A | Enzyme | C00006935 C00006961 C00008155 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00006935 C00006961 C00008155 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00006935 C00006961 C00008155 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00006935 C00006961 C00008155 | 4 / 3 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00006935 C00006961 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006934 C00008155 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00006935 C00008155 | 2 / 5 |
P11473 | Vitamin D3 receptor | NR1I1 | C00006961 C00008155 | 2 / 3 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00006935 C00006961 | 1 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00006935 C00008155 | 1 / 2 |
Q99700 | Ataxin-2 | Unclassified protein | C00006935 C00006961 | 1 / 1 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00006935 C00006961 | 7 / 3 |
Q9Y253 | DNA polymerase eta | Enzyme | C00006961 C00008155 | 1 / 1 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00006935 C00006961 | 0 / 0 |
P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00008155 | 3 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00008155 | 0 / 0 |
P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00008155 | 0 / 0 |
P10696 | Alkaline phosphatase, placental-like | Enzyme | C00008155 | 0 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00006934 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00006935 | 2 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00008155 | 0 / 0 |
Q15056 | Eukaryotic translation initiation factor 4H | Unclassified protein | C00008155 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00006934 | 0 / 1 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00008155 | 1 / 1 |
P11940 | Polyadenylate-binding protein 1 | Unclassified protein | C00008155 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00006961 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00008155 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00008155 | 0 / 0 |
P22001 | Potassium voltage-gated channel subfamily A member 3 | KCNA, Kv1.x (Shaker) | C00006935 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00008155 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00008155 | 2 / 1 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00006961 | 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
|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#146300 | Hypophosphatasia, adult |
P05186
|
#241510 | Hypophosphatasia, childhood |
P05186
|
#241500 | Hypophosphatasia, infantile |
P05186
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H00213 | Hypophosphatasia |
P05186
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00023 | Testicular cancer |
P10696
(marker)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|