Organism name | Bacillus subtilis |
---|---|
Genus | Bacillus |
Family | Bacillaceae |
Kingdom | Bacteria |
Linked NCBI taxonomy name | Bacillus subtilis |
---|---|
Linked NCBI taxonomy ID | 1423 |
Linked level | species |
Family in NCBI taxonomy | Bacillaceae |
---|---|
ID | 186817 |
Kingdom (Superkingdom) in NCBI taxonomy | Bacteria |
---|---|
ID | 2 |
Plant class | |
---|---|
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 |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00019756
![]() |
Daidzein 7-O-(6''-succinylglucoside)
/ 7,4'-Dihydroxyisoflavone 7-O-(6''-succinylglucoside) |
No. 2 | No. 15 |
![]() |
||||
C00019757
![]() |
Genistein 7-O-(6''-succinylglucoside)
/ 5,7,4'-Trihydroxyisoflavone 7-O-(6''-succinylglucoside) |
No. 2 | No. 15 |
![]() |
||||
C00019758
![]() |
Glycitein 7-O-(6''-succinylglucoside)
/ 7,4'-Dihydroxy-6-methoxyisoflavone 7-O-(6''-succinylglucoside) |
No. 2 | No. 15 |
![]() |
||||
C00029420
![]() |
1-Deoxynojirimycin
/ (+)-1-Deoxynojirimycin |
CHEMBL11510
CHEMBL65131 CHEMBL307429 CHEMBL84844 CHEMBL110458 CHEMBL369297 CHEMBL179085 CHEMBL176206 CHEMBL179130 CHEMBL179347 CHEMBL179409 CHEMBL176021 CHEMBL369046 CHEMBL176209 CHEMBL368121 CHEMBL175901 CHEMBL1337303 |
D017485
|
33 / 27 / 27 | No. 786 | No. 1 |
![]() |
|
C00002669
![]() |
Pyrocatechuic acid
/ o-Pyrocatechuic acid / 2,3-Dihydroxybenzoic acid |
CHEMBL1432
|
C009135
|
12 / 6 / 5 | 1 / 4 | No. 817 | No. 81 |
![]() |
C00000757
![]() |
Dethiobiotin
|
CHEMBL1232381
|
11 / 11 / 7 | No. 3747 |
![]() |
|||
C00000734
![]() |
Isochorismic acid
|
C052985
|
No. 3811 |
![]() |
||||
C00000733
![]() |
Chorismic acid
|
CHEMBL1160745
|
D002827
|
No. 3811 |
![]() |
|||
C00007494
![]() |
4-Amino-5-hydroxymethyl-2-methylpyrimidine
|
C012068
|
No. 5580 |
![]() |
||||
C00000759
![]() |
7,8-Diaminopelargonic acid
|
No. 5903 |
![]() |
|||||
C00016740
![]() |
Bacitracin F
|
C037039
|
No. 6080 |
![]() |
||||
C00000758
![]() |
8-Amino-7-oxopelargonic acid
|
No. 8032 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
O75164 | Lysine-specific demethylase 4A | Enzyme | C00000757 C00002669 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00029420 | 1 / 1 |
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00002669 | 0 / 0 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | C00029420 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00029420 | 6 / 4 |
Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00029420 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00029420 | 1 / 1 |
P22894 | Neutrophil collagenase | M10A | C00002669 | 0 / 0 |
Q9H227 | Cytosolic beta-glucosidase | Enzyme | C00029420 | 0 / 0 |
P14780 | Matrix metalloproteinase-9 | M10A | C00002669 | 2 / 2 |
Q9Y5X4 | Photoreceptor-specific nuclear receptor | NR2E3 | C00000757 | 2 / 2 |
P35573 | Glycogen debranching enzyme | Enzyme | C00029420 | 1 / 1 |
P14735 | Insulin-degrading enzyme | Enzyme | C00000757 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00029420 | 3 / 1 |
P16278 | Beta-galactosidase | Enzyme | C00029420 | 4 / 6 |
P02768 | Serum albumin | Secreted protein | C00002669 | 0 / 0 |
P04066 | Tissue alpha-L-fucosidase | Enzyme | C00029420 | 1 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00029420 | 0 / 1 |
P23458 | Tyrosine-protein kinase JAK1 | Jakb | C00029420 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00029420 | 0 / 0 |
P16581 | E-selectin | Adhesion | C00002669 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000757 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00000757 | 0 / 0 |
P14410 | Sucrase-isomaltase, intestinal | Enzyme | C00029420 | 1 / 1 |
P03956 | Interstitial collagenase | M10A | C00002669 | 0 / 1 |
Q9Y253 | DNA polymerase eta | Enzyme | C00000757 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00000757 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00002669 | 1 / 1 |
Q13133 | Oxysterols receptor LXR-alpha | NR1H3 | C00029420 | 0 / 0 |
O00462 | Beta-mannosidase | Enzyme | C00029420 | 1 / 2 |
Q9HCG7 | Non-lysosomal glucosylceramidase | Enzyme | C00029420 | 1 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00029420 | 0 / 0 |
P08253 | 72 kDa type IV collagenase | M10A | C00002669 | 1 / 3 |
P55055 | Oxysterols receptor LXR-beta | NR1H3 | C00029420 | 0 / 0 |
P09848 | Lactase-phlorizin hydrolase | Enzyme | C00029420 | 1 / 1 |
Q16739 | Ceramide glucosyltransferase | Transferase | C00029420 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00029420 | 0 / 0 |
P14151 | L-selectin | Adhesion | C00002669 | 0 / 0 |
P16109 | P-selectin | Adhesion | C00002669 | 1 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00029420 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00029420 | 0 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00029420 | 1 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00029420 | 0 / 0 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00029420 | 0 / 0 |
O43280 | Trehalase | Enzyme | C00029420 | 0 / 0 |
P08254 | Stromelysin-1 | M10A | C00002669 | 1 / 0 |
O00754 | Lysosomal alpha-mannosidase | Enzyme | C00029420 | 1 / 2 |
Q6P4F1 | Alpha-(1,3)-fucosyltransferase 10 | Enzyme | C00029420 | 0 / 0 |
Q9Y2E5 | Epididymis-specific alpha-mannosidase | Enzyme | C00029420 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00000757 | 1 / 0 |
O00255 | Menin | Unclassified protein | C00029420 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00029420 | 1 / 2 |
P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00000757 | 5 / 3 |
Q9Y618 | Nuclear receptor corepressor 2 | Unclassified protein | C00000757 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00000757 | 2 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
4313 | MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 | matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) |
C00002669
|
OMIM | preferred title | UniProt |
---|---|---|
%606641 | Body mass index; bmi |
P37231
|
#609338 | Carotid intimal medial thickness 1 |
P37231
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#614466 | Coronary heart disease, susceptibility to, 6; chds6 |
P08254
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#268100 | Enhanced s-cone syndrome; escs |
Q9Y5X4
|
#301500 | Fabry disease |
P06280
|
#230000 | Fucosidosis |
P04066
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
P37231 |
#232300 | Glycogen storage disease ii |
P10253
|
#232400 | Glycogen storage disease iii |
P35573
|
#230500 | Gm1-gangliosidosis, type i |
P16278
|
#230600 | Gm1-gangliosidosis, type ii |
P16278
|
#230650 | Gm1-gangliosidosis, type iii |
P16278
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603932 | Intervertebral disc disease; idd |
P14780
|
#223000 | Lactase deficiency, congenital |
P09848
|
#604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248500 | Mannosidosis, alpha b, lysosomal; mansa |
O00754
|
#248510 | Mannosidosis, beta a, lysosomal; mansb |
O00462
|
#613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
#253010 | Mucopolysaccharidosis type ivb |
P16278
|
#259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#601665 | Obesity |
P37231
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#611131 | Retinitis pigmentosa 37; rp37 |
Q9Y5X4
|
#614409 | Spastic paraplegia 46, autosomal recessive; spg46 |
Q9HCG7
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601367 | Stroke, ischemic |
P16109
|
#222900 | Sucrase-isomaltase deficiency, congenital; csid |
P14410
|
#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
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
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)
|
H00140 | beta-Mannosidosis |
O00462
(related)
|
H00422 | Glycoproteinoses |
O00462
(related)
O00754 (related) P04066 (related) P16278 (related) |
H00139 | alpha-Mannosidosis |
O00754
(related)
|
H00028 | Choriocarcinoma |
P03956
(related)
P08253 (related) |
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
P16278 (related) |
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00141 | Fucosidosis |
P04066
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00025 | Penile cancer |
P08253
(related)
P14780 (related) |
H00472 | Torg-Winchester syndrome |
P08253
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00116 | Congenital lactase deficiency |
P09848
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
P35573 (related) |
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|
H00479 | Metaphyseal dysplasias |
P14780
(related)
|
H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
H00276 | Galactosialidosis |
P16278
(related)
|
H00281 | GM1 gangliosidosis |
P16278
(related)
|
H00421 | Mucopolysaccharidosis (MPS) |
P16278
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00032 | Thyroid cancer |
P37231
(related)
|
H00409 | Type II diabetes mellitus |
P37231
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P37231
(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)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|
H00527 | Retinitis pigmentosa (RP) |
Q9Y5X4
(related)
|
H00805 | Vitreoretinal degeneration |
Q9Y5X4
(related)
|