Organism name | Ampullariella regularis A11079 |
---|---|
Genus | Ampullariella |
Family | Actinoplanaceae |
Kingdom | Bacteria |
Linked NCBI taxonomy name | Actinoplanes |
---|---|
Linked NCBI taxonomy ID | 1865 |
Linked level | genus |
Family in NCBI taxonomy | Micromonosporaceae |
---|---|
ID | 28056 |
Kingdom (Superkingdom) in NCBI taxonomy | Bacteria |
---|---|
ID | 2 |
Plant class | |
---|---|
ID |
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 |
---|---|---|---|---|---|---|---|---|
C00018327
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Neplanocin A
/ (-)-Neplanocin A |
CHEMBL8771
CHEMBL9568 CHEMBL338953 CHEMBL128192 |
C031096
|
10 / 14 / 10 | No. 1060 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P23526 | Adenosylhomocysteinase | Enzyme | C00018327 | 1 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00018327 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00018327 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00018327 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00018327 | 7 / 3 |
P51843 | Nuclear receptor subfamily 0 group B member 1 | Nuclear hormone receptor subfamily 0 group B member 1 | C00018327 | 2 / 2 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00018327 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00018327 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00018327 | 1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00018327 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#300018 | 46,xy sex reversal 2; srxy2 |
P51843
|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#300200 | Adrenal hypoplasia, congenital; ahc |
P51843
|
#114500 | Colorectal cancer; crc |
P84022
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#613752 | Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency |
P23526
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#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
|
KEGG | name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00184 | Hypermethioninemia |
P23526
(related)
|
H00552 | Glycerol kinase deficiency (GKD) |
P51843
(related)
|
H00607 | 46,XY disorders of sex development (Disorders of gonadal development) |
P51843
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|