Species

KNApSAcK Entry

Organism name Bacillus subtilis
Genus Bacillus
Family Bacillaceae
Kingdom Bacteria

NCBI taxonomy

Entry

Linked NCBI taxonomy name Bacillus subtilis
Linked NCBI taxonomy ID 1423
Linked level species

Family

Family in NCBI taxonomy Bacillaceae
ID 186817

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Bacteria
ID 2

Plant class

Plant class
ID

Metabolite list (12)

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 External link 512 Daidzein 7-O-(6''-succinylglucoside)
/ 7,4'-Dihydroxyisoflavone 7-O-(6''-succinylglucoside)
No. 2 No. 15
C00019757 External link 512 Genistein 7-O-(6''-succinylglucoside)
/ 5,7,4'-Trihydroxyisoflavone 7-O-(6''-succinylglucoside)
No. 2 No. 15
C00019758 External link 512 Glycitein 7-O-(6''-succinylglucoside)
/ 7,4'-Dihydroxy-6-methoxyisoflavone 7-O-(6''-succinylglucoside)
No. 2 No. 15
C00029420 External link 512 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 External link 512 Pyrocatechuic acid
/ o-Pyrocatechuic acid
/ 2,3-Dihydroxybenzoic acid
CHEMBL1432
C009135
12 / 6 / 5 1 / 4 No. 817 No. 81
C00000757 External link 512 Dethiobiotin
CHEMBL1232381
11 / 11 / 7 No. 3747
C00000734 External link 512 Isochorismic acid
C052985
No. 3811
C00000733 External link 512 Chorismic acid
CHEMBL1160745
D002827
No. 3811
C00007494 External link 512 4-Amino-5-hydroxymethyl-2-methylpyrimidine
C012068
No. 5580
C00000759 External link 512 7,8-Diaminopelargonic acid
No. 5903
C00016740 External link 512 Bacitracin F
C037039
No. 6080
C00000758 External link 512 8-Amino-7-oxopelargonic acid
No. 8032

Human Protein / Gene in interactions

55 ChEMBL Protein in interactions

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

1 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (44)

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 DISEASE (39)

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)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D058186 Acute Kidney Injury C00002669
D034381 Hearing Loss C00002669
D007674 Kidney Diseases C00002669
D015837 Vestibular Diseases C00002669