Lycopersicon esculentum var.cerasiforme (DUNAL) ALEF.
Species
KNApSAcK Entry
| Organism name | Lycopersicon esculentum var.cerasiforme (DUNAL) ALEF. |
|---|---|
| Genus | Lycopersicon |
| Family | Solanaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Lycopersicon |
|---|---|
| Linked NCBI taxonomy ID | 49274 |
| Linked level | subgenus |
Family
| Family in NCBI taxonomy | Solanaceae |
|---|---|
| ID | 4070 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | asterids |
|---|---|
| ID | 71274 |
Metabolite list (6)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00030698
|
Lycoperoside G
|
No. 21 | No. 11 |
|
||||
|
C00030216
|
Esculeoside A
|
CHEMBL1269162
|
No. 21 | No. 11 |
|
|||
|
C00030217
|
Esculeoside B
|
No. 21 | No. 11 |
|
||||
|
C00030219
|
Esculeoside D
|
No. 21 | No. 11 |
|
||||
|
C00030218
|
Esculeoside C
|
No. 21 | No. 11 |
|
||||
|
C00001386
|
L-Phenylalanine
|
CHEMBL25080
CHEMBL301523 CHEMBL379630 |
27 / 18 / 14 | No. 3303 |
|
Human Protein / Gene in interactions
27 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001386 | 1 / 0 |
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00001386 | 2 / 0 |
| Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00001386 | 0 / 0 |
| P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00001386 | 0 / 0 |
| P43166 | Carbonic anhydrase 7 | Lyase | C00001386 | 0 / 0 |
| Q9Y263 | Phospholipase A-2-activating protein | Unclassified protein | C00001386 | 0 / 0 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00001386 | 3 / 1 |
| P00918 | Carbonic anhydrase 2 | Lyase | C00001386 | 1 / 2 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001386 | 0 / 1 |
| P23280 | Carbonic anhydrase 6 | Lyase | C00001386 | 0 / 0 |
| Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00001386 | 0 / 0 |
| O43570 | Carbonic anhydrase 12 | Lyase | C00001386 | 1 / 2 |
| P00915 | Carbonic anhydrase 1 | Lyase | C00001386 | 0 / 0 |
| P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00001386 | 0 / 0 |
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00001386 | 3 / 1 |
| P04150 | Glucocorticoid receptor | NR3C1 | C00001386 | 0 / 1 |
| P14679 | Tyrosinase | Oxidoreductase | C00001386 | 4 / 2 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001386 | 0 / 0 |
| Q16790 | Carbonic anhydrase 9 | Lyase | C00001386 | 0 / 1 |
| P03372 | Estrogen receptor | NR3A1 | C00001386 | 1 / 1 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001386 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001386 | 0 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001386 | 0 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00001386 | 0 / 0 |
| P07451 | Carbonic anhydrase 3 | Lyase | C00001386 | 0 / 0 |
| P22748 | Carbonic anhydrase 4 | Lyase | C00001386 | 1 / 1 |
| Q05BR4 | SLC16A10 protein | Unclassified protein | C00001386 | 0 / 0 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (18)
| OMIM | preferred title | UniProt |
|---|---|---|
| #103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
| #203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
| #606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #615363 | Estrogen resistance; estrr |
P03372
|
| #143860 | Hyperchlorhidrosis, isolated |
O43570
|
| #146300 | Hypophosphatasia, adult |
P05186
|
| #241510 | Hypophosphatasia, childhood |
P05186
|
| #241500 | Hypophosphatasia, infantile |
P05186
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #600852 | Retinitis pigmentosa 17; rp17 |
P22748
|
| #604906 | Schizophrenia 9; sczd9 |
P49798
|
| #181500 | Schizophrenia; sczd |
P49798
|
| #601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
KEGG DISEASE (14)
| KEGG | name | UniProt |
|---|---|---|
| H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
| H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| H00026 | Endometrial Cancer |
P03372
(marker)
|
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
| H00213 | Hypophosphatasia |
P05186
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
| H00038 | Malignant melanoma |
P14679
(marker)
|
| H00527 | Retinitis pigmentosa (RP) |
P22748
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|