class name | count |
---|---|
rosids | 10 |
Euphyllophyta | 6 |
eudicotyledons | 2 |
Spermatophyta | 1 |
class name | count |
---|---|
Dennstaedtiaceae | 5 |
Sapindaceae | 3 |
Anacardiaceae | 3 |
Hippocastanaceae | 2 |
Ranunculaceae | 2 |
Ginkgoaceae | 1 |
Brassicaceae | 1 |
Enterobacteriaceae | 1 |
Aceraceae | 1 |
Pteridaceae | 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 |
KCF-S
cluster |
figure |
---|---|---|---|---|---|---|---|
C00021448
![]() |
Protoanemonin
/ Protoanemonene |
C037354
|
No. 2532 |
![]() |
|||
C00021445
![]() |
L-gamma-Glutamyl-L-cysteine
|
CHEMBL460831
|
C017341
|
No. 2532 |
![]() |
||
C00021444
![]() |
L-gamma-Glutamyl-L-hypoglycin
|
No. 2532 |
![]() |
||||
C00021443
![]() |
alpha-(Methylenecyclopropyl)glycine
|
C059830
|
No. 2532 |
![]() |
|||
C00002635
![]() |
Anacardic acid
|
CHEMBL33778
|
1 / 0 / 0 | No. 3375 |
![]() |
||
C00002651
![]() |
Ginkgoic acid
|
CHEMBL277156
CHEMBL445177 |
C112485
|
11 / 9 / 9 | No. 3375 |
![]() |
|
C00002681
![]() |
Urushiol III
|
No. 3375 |
![]() |
||||
C00001372
![]() |
Hypoloside B
|
C062113
|
No. 5046 |
![]() |
|||
C00001381
![]() |
Hypoloside C
|
No. 5046 |
![]() |
||||
C00007507
![]() |
L-Hypoglycin
|
CHEMBL1615355
|
C041757
|
No. 5121 |
![]() |
||
C00001360
![]() |
Hypoloside A
|
No. 5121 |
![]() |
||||
C00000301
![]() |
Braxin C
/ Ptaquiloside |
C043680
|
11 / 1 | No. 8338 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UBE0 | SUMO-activating enzyme subunit 1 | Unclassified protein | C00002635 C00002651 | 0 / 0 |
P13726 | Tissue factor | Membrane receptor | C00002651 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002651 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00002651 | 2 / 3 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002651 | 0 / 0 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002651 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002651 | 3 / 3 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002651 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002651 | 4 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00002651 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002651 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
308 | ANXA5, ANX5, ENX2, PP4, RPRGL3 | annexin A5 |
C00021448
|
1111 | CHEK1, CHK1 | checkpoint kinase 1 (EC:2.7.11.1) |
C00021448
|
1649 | DDIT3, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 | DNA-damage-inducible transcript 3 |
C00021448
|
1647 | GADD45A, DDIT1, GADD45 | growth arrest and DNA-damage-inducible, alpha |
C00021448
|
5608 | MAP2K6, MAPKK6, MEK6, MKK6, PRKMK6, SAPKK-3, SAPKK3 | mitogen-activated protein kinase kinase 6 (EC:2.7.12.2) |
C00021448
|
4683 | NBN, AT-V1, AT-V2, ATV, NBS, NBS1, P95 | nibrin |
C00021448
|
10111 | RAD50, NBSLD, RAD502, hRad50 | RAD50 homolog (S. cerevisiae) |
C00021448
|
5890 | RAD51B, R51H2, RAD51L1, REC2 | RAD51 paralog B |
C00021448
|
27244 | SESN1, PA26, SEST1 | sestrin 1 |
C00021448
|
7157 | TP53, BCC7, LFS1, P53, TRP53 | tumor protein p53 |
C00021448
|
7508 | XPC, RAD4, XP3, XPCC | xeroderma pigmentosum, complementation group C |
C00021448
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(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)
|