class name | count |
---|---|
asterids | 9 |
class name | count |
---|---|
Theaceae | 9 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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
![]() |
Theaflavin
|
CHEMBL346119
CHEMBL403814 CHEMBL1512440 |
C056068
|
21 / 20 / 31 | 10 / 3 |
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C00009349
![]() |
Theaflavin 3-O-gallate
|
CHEMBL253536
|
1 / 0 / 7 |
![]() |
||
C00009350
![]() |
Theaflavin 3'-O-gallate
|
CHEMBL423795
|
![]() |
|||
C00009351
![]() |
Theaflavin 3,3'-di-O-gallate
|
CHEMBL434864
CHEMBL402609 CHEMBL1451483 |
26 / 35 / 43 |
![]() |
||
C00009353
![]() |
Epitheaflagallin 3-O-gallate
|
CHEMBL349707
|
![]() |
|||
C00009354
![]() |
Oolongtheanin
|
CHEMBL159756
|
![]() |
|||
C00041068
![]() |
Neotheaflavin 3-O-gallate
|
CHEMBL253536
|
1 / 0 / 7 |
![]() |
||
C00041209
![]() |
Theaflavate B
|
![]() |
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 |
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
|
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 | 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)
|