Species

KNApSAcK Entry

Organism name Marchantia berteroana
Genus Marchantia
Family Marchantiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Marchantia
Linked NCBI taxonomy ID 3196
Linked level genus

Family

Family in NCBI taxonomy Marchantiaceae
ID 29585

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Embryophyta
ID 3193

Metabolite list (11)

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
C00004302 External link 512 Luteolin 3',4'-digalacturonide
No. 1 No. 15
C00004423 External link 512 8-Hydroxyluteolin 8,4'-diglucuronide
No. 1 No. 15
C00004293 External link 512 Luteolin 7,3'-digalacturonide
No. 1 No. 15
C00004269 External link 512 Luteolin 7-galacturonide
CHEMBL464224
No. 2 No. 15
C00004246 External link 512 Isoscutellarein 8-glucuronide
CHEMBL462705
No. 2 No. 15
C00004420 External link 512 8-Hydroxyluteolin 8-glucuronide
CHEMBL512433
No. 2 No. 15
C00004145 External link 512 Apigenin 7-galacturonide
CHEMBL254213
CHEMBL1980748
No. 2 No. 15
C00004275 External link 512 Luteolin 3'-galacturonide
No. 2 No. 15
C00008048 External link 512 Aureusidin 6-glucuronide
No. 12 No. 14
C00002889 External link 512 Lunularin
/ 3,4'-Dihydroxybibenzyl
CHEMBL445252
C121619
No. 242 No. 26
C00001120 External link 512 D-Galacturonic acid
CHEMBL496672
CHEMBL1159524
CHEMBL2068684
13 / 14 / 14 No. 4351

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001120 1 / 0
P02545 Prelamin-A/C Unclassified protein C00001120 11 / 10
P02768 Serum albumin Secreted protein C00001120 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001120 0 / 1
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001120 0 / 0
O75496 Geminin Unclassified protein C00001120 0 / 0
Q8TCC7 Solute carrier family 22 member 8 Antiporter C00001120 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001120 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001120 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001120 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00001120 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001120 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001120 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#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
#275210 Restrictive dermopathy, lethal P02545
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (14)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (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)
H01171 Poor drug metabolism (PM) P33261 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)