Plant Species


Cumulative plant class count

class name count
asterids 9

Cumulative family count

class name count
Theaceae 9

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (8)

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
C00009348 External link 512 Theaflavin
CHEMBL346119
CHEMBL403814
CHEMBL1512440
C056068
21 / 20 / 31 10 / 3
C00009349 External link 512 Theaflavin 3-O-gallate
CHEMBL253536
1 / 0 / 7
C00009350 External link 512 Theaflavin 3'-O-gallate
CHEMBL423795
C00009351 External link 512 Theaflavin 3,3'-di-O-gallate
CHEMBL434864
CHEMBL402609
CHEMBL1451483
26 / 35 / 43
C00009353 External link 512 Epitheaflagallin 3-O-gallate
CHEMBL349707
C00009354 External link 512 Oolongtheanin
CHEMBL159756
C00041068 External link 512 Neotheaflavin 3-O-gallate
CHEMBL253536
1 / 0 / 7
C00041209 External link 512 Theaflavate B

Human Protein / Gene in interactions

26 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10415 Apoptosis regulator Bcl-2 Other cytosolic protein C00009348 C00009349 C00009351 C00041068 0 / 7
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00009348 C00009351 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00009348 C00009351 1 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00009348 C00009351 3 / 1
P54132 Bloom syndrome protein Enzyme C00009348 C00009351 1 / 2
P51570 Galactokinase Enzyme C00009348 C00009351 1 / 1
P11473 Vitamin D3 receptor NR1I1 C00009348 C00009351 2 / 3
O00255 Menin Unclassified protein C00009348 C00009351 2 / 5
Q92830 Histone acetyltransferase KAT2A Enzyme C00009348 C00009351 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00009348 C00009351 1 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00009348 C00009351 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00009348 C00009351 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00009348 C00009351 3 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00009348 C00009351 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00009348 C00009351 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00009348 C00009351 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00009348 C00009351 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00009348 C00009351 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00009348 C00009351 4 / 3
P29466 Caspase-1 C14 C00009348 C00009351 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00009348 C00009351 2 / 2
P55210 Caspase-7 C14 C00009351 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00009351 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00009351 4 / 2
O15296 Arachidonate 15-lipoxygenase B Enzyme C00009351 0 / 0
P02545 Prelamin-A/C Unclassified protein C00009351 11 / 10

10 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
581 BAX, BCL2L4 BCL2-associated X protein C00009348
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00009348
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00009348
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00009348
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00009348
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00009348
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00009348
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00009348
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00009348
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00009348

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (35)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#210900 Bloom syndrome; blm P54132
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600274 Frontotemporal dementia; ftd P10636
#230200 Galactokinase deficiency P51570
#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
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (43)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
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)
H00005 Chronic lymphocytic leukemia (CLL) P10415 (related)
H00013 Small cell lung cancer P10415 (related)
H00018 Gastric cancer P10415 (related)
H00028 Choriocarcinoma P10415 (related)
H00030 Cervical cancer P10415 (related)
H00041 Kaposi's sarcoma P10415 (related)
H00054 Nasopharyngeal cancer P10415 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (related)
H00070 Galactosemia P51570 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (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)
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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006965 Hyperplasia C00009348
D007249 Inflammation C00009348
D011471 Prostatic Neoplasms C00009348