Species

KNApSAcK Entry

Organism name Ampullariella regularis A11079
Genus Ampullariella
Family Actinoplanaceae
Kingdom Bacteria

NCBI taxonomy

Entry

Linked NCBI taxonomy name Actinoplanes
Linked NCBI taxonomy ID 1865
Linked level genus

Family

Family in NCBI taxonomy Micromonosporaceae
ID 28056

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Bacteria
ID 2

Plant class

Plant class
ID

Metabolite list (1)

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 External link 512 Neplanocin A
/ (-)-Neplanocin A
CHEMBL8771
CHEMBL9568
CHEMBL338953
CHEMBL128192
C031096
10 / 14 / 10 No. 1060

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

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 DISEASE (10)

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)