PCIDB

Cuscuta reflexa

Species

KNApSAcK Entry

Organism name Cuscuta reflexa
Genus Cuscuta
Family Convolvulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Cuscuta reflexa
Linked NCBI taxonomy ID 4129
Linked level species

Family

Family in NCBI taxonomy Convolvulaceae
ID 4118

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

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
C00032667 External link 512 6,7,8-Trimethoxy-2H-1-benzopyran-2-one
CHEMBL253551
10 / 7 / 9 No. 364 No. 25

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P43166 Carbonic anhydrase 7 Lyase C00032667 0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase C00032667 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00032667 1 / 2
P00352 Retinal dehydrogenase 1 Enzyme C00032667 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00032667 1 / 2
P00915 Carbonic anhydrase 1 Lyase C00032667 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00032667 0 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00032667 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00032667 2 / 2
B2RXH2 Lysine-specific demethylase 4E Enzyme C00032667 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#119900 Digital clubbing, isolated congenital P15428
#143860 Hyperchlorhidrosis, isolated O43570
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918

KEGG DISEASE (9)

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)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)