PCIDB

Streptomyces tubercidicus

Species

KNApSAcK Entry

Organism name Streptomyces tubercidicus
Genus Streptomyces
Family Streptomycetaceae
Kingdom Bacteria

NCBI taxonomy

Entry

Linked NCBI taxonomy name Streptomyces tubercidicus
Linked NCBI taxonomy ID 47759
Linked level species

Family

Family in NCBI taxonomy Streptomycetaceae
ID 2062

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
C00018670 External link 512 U 10071
/ Tubercidine
/ Sparsamycin A
/ 7-Deazaadenosine
/ Antibiotic XK 101-1
CHEMBL267099
CHEMBL599189
CHEMBL2093914
CHEMBL2311082
D014372
12 / 13 / 5 No. 1761

Human Protein / Gene in interactions

12 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00018670 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00018670 2 / 0
O75496 Geminin Unclassified protein C00018670 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00018670 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00018670 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00018670 0 / 0
P55263 Adenosine kinase Enzyme C00018670 1 / 0
P00491 Purine nucleoside phosphorylase Enzyme C00018670 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00018670 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00018670 0 / 0
Q53EL6 Programmed cell death protein 4 Unclassified protein C00018670 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00018670 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114500 Colorectal cancer; crc P84022
#137800 Glioma susceptibility 1; glm1 O75874
#614300 Hypermethioninemia due to adenosine kinase deficiency P55263
#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
#613179 Purine nucleoside phosphorylase deficiency P00491
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (5)

KEGG name UniProt
H00093 Combined immunodeficiencies (CIDs) P00491 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)