Species

KNApSAcK Entry

Organism name Arthrinium phaeospermum T-53
Genus Arthrinium
Family Lasiosphaeriaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Arthrinium
Linked NCBI taxonomy ID 112177
Linked level genus

Family

Family in NCBI taxonomy Apiosporaceae
ID 106263

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

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
C00018064 External link 512 NSC 139979
/ L-threo-3-Hydroxyaspartic acid
/ L-threo-beta-Hydroxyaspartic acid
CHEMBL568192
CHEMBL1231330
CHEMBL1256517
CHEMBL1356625
14 / 6 / 7 No. 5453

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00018064 1 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00018064 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00018064 3 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00018064 0 / 1
P54132 Bloom syndrome protein Enzyme C00018064 1 / 2
P00352 Retinal dehydrogenase 1 Enzyme C00018064 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00018064 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00018064 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00018064 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00018064 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00018064 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00018064 0 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00018064 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00018064 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (7)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)