Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Enterobacteriaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK 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
figure
C00019561 External link 512 PPi
/ Diphosphoric acid
/ Pyrophosphoric acid
CHEMBL1160571
C107241
10 / 5 / 7

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00019561 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00019561 0 / 1
P54132 Bloom syndrome protein Enzyme C00019561 1 / 2
P00480 Ornithine carbamoyltransferase, mitochondrial Enzyme C00019561 1 / 1
P14324 Farnesyl pyrophosphate synthase Transferase C00019561 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00019561 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00019561 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00019561 0 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00019561 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00019561 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#311250 Ornithine transcarbamylase deficiency, hyperammonemia due to P00480
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (7)

KEGG name UniProt
H00187 Ornithine transcarbamylase deficiency P00480 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)