PCIDB

KCF-S cluster No. 3843 (3 metabolites)

Plant Species

Cumulative plant class count

class name count
rosids 5

Cumulative family count

class name count
Brassicaceae 3
Fabaceae 2
Enterobacteriaceae 2

KEGG BRITE br08003 External link 512

Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (3)

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
C00001341 External link 512 L-Asparagine
CHEMBL58832
CHEMBL1232369
1 / 2 / 0
C00001359 External link 512 L-Glutamine
CHEMBL930
CHEMBL1232207
14 / 23 / 20
C00034027 External link 512 L-Asparaginate
CHEMBL58832
CHEMBL1232369
1 / 2 / 0

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001341 C00034027 2 / 0
P39748 Flap endonuclease 1 Enzyme C00001359 0 / 0
P02545 Prelamin-A/C Unclassified protein C00001359 11 / 10
P16473 Thyrotropin receptor Glycohormone receptor C00001359 3 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001359 0 / 1
P54132 Bloom syndrome protein Enzyme C00001359 1 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001359 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001359 1 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001359 1 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001359 0 / 0
Q01453 Peripheral myelin protein 22 Unclassified protein C00001359 5 / 2
P16050 Arachidonate 15-lipoxygenase Enzyme C00001359 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001359 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001359 0 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001359 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798

KEGG DISEASE (20)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
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)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)