Species

KNApSAcK Entry

Organism name Betula spp.
Genus Betula
Family Betulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Betula
Linked NCBI taxonomy ID 3504
Linked level genus

Family

Family in NCBI taxonomy Betulaceae
ID 3514

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (13)

Species Activity
Betula spp. Analgesic
Betula spp. Antibacterial
Betula spp. Antiinflammatory
Betula spp. Antimelanomic
Betula spp. Antipyretic
Betula spp. Antiseptic
Betula spp. Aquaretic
Betula spp. Astringent
Betula spp. Couterirritant
Betula spp. Depurative
Betula spp. Diuretic
Betula spp. Parasiticide
Betula spp. Saluretic

Metabolite list (9)

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
C00009070 External link 512 Procyanidin B6
/ Catechin-(4alpha->6)-catechin
CHEMBL506487
CHEMBL502984
CHEMBL451115
No. 16 No. 19
C00008226 External link 512 Naringenin 7,4'-dimethyl ether
CHEMBL462909
CHEMBL2164944
No. 25 No. 14
C00000999 External link 512 Sakuranetin
/ Naringenin 7-O-methyl ether
/ 5,4'-Dihydroxy-7-methoxyflavanone
CHEMBL74852
CHEMBL448297
C099724
19 / 20 / 20 No. 25 No. 14
C00009089 External link 512 Arecatannin B1
CHEMBL592329
2 / 3 / 4 No. 29 No. 19
C00009086 External link 512 Epicatechin-(4beta->6)-epicatechin-(4beta->8)-catechin
CHEMBL592228
2 / 3 / 4 No. 29 No. 19
C00009091 External link 512 Procyanidin C2
CHEMBL290632
13 / 5 / 6 No. 29 No. 19
C00009094 External link 512 Catechin-(4alpha->8)-epicatechin-(4beta->8)-epicatechin
CHEMBL290632
13 / 5 / 6 No. 29 No. 19
C00009097 External link 512 Arecatamnin A1
/ [Epicatechin-(4beta->8)]2-catechin
CHEMBL290632
13 / 5 / 6 No. 29 No. 19
C00009098 External link 512 Procyanidin C1
/ [Epicatechin-(4beta->8)]2-epicatechin
CHEMBL290632
13 / 5 / 6 No. 29 No. 19

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14780 Matrix metalloproteinase-9 M10A C00009086 C00009089 C00009091 C00009094 C00009097 C00009098 2 / 2
P08253 72 kDa type IV collagenase M10A C00009086 C00009089 C00009091 C00009094 C00009097 C00009098 1 / 3
P41743 Protein kinase C iota type Iota C00009091 C00009094 C00009097 C00009098 0 / 0
P24723 Protein kinase C eta type Eta C00009091 C00009094 C00009097 C00009098 1 / 0
P05771 Protein kinase C beta type Alpha C00009091 C00009094 C00009097 C00009098 0 / 0
P05129 Protein kinase C gamma type Alpha C00009091 C00009094 C00009097 C00009098 1 / 1
Q15139 Serine/threonine-protein kinase D1 Pkd C00009091 C00009094 C00009097 C00009098 0 / 0
P17252 Protein kinase C alpha type Alpha C00009091 C00009094 C00009097 C00009098 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00009091 C00009094 C00009097 C00009098 0 / 0
Q02156 Protein kinase C epsilon type Eta C00009091 C00009094 C00009097 C00009098 0 / 0
Q04759 Protein kinase C theta type Delta C00009091 C00009094 C00009097 C00009098 0 / 1
Q05513 Protein kinase C zeta type Iota C00009091 C00009094 C00009097 C00009098 0 / 0
Q05655 Protein kinase C delta type Delta C00009091 C00009094 C00009097 C00009098 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000999 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000999 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000999 4 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00000999 0 / 0
P59538 Taste receptor type 2 member 31 Taste receptor (taste family GPCR) C00000999 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00000999 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00000999 1 / 4
Q9Y253 DNA polymerase eta Enzyme C00000999 1 / 1
O75496 Geminin Unclassified protein C00000999 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000999 2 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000999 0 / 0
Q9Y3R4 Sialidase-2 Enzyme C00000999 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000999 2 / 3
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00000999 1 / 4
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000999 0 / 0
Q99700 Ataxin-2 Unclassified protein C00000999 1 / 1
P04062 Glucosylceramidase Enzyme C00000999 6 / 4
P33765 Adenosine receptor A3 Adenosine receptor C00000999 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000999 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#208900 Ataxia-telangiectasia; at Q13315
#114500 Colorectal cancer; crc P84022
#600274 Frontotemporal dementia; ftd P10636
#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
#603932 Intervertebral disc disease; idd P14780
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#605361 Spinocerebellar ataxia 14; sca14 P05129
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P24723
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (25)

KEGG name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
Q99700 (related)
Q9NUW8 (related)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00028 Choriocarcinoma P08253 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (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)
H00479 Metaphyseal dysplasias P14780 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00408 Type I diabetes mellitus Q04759 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)