Species

KNApSAcK Entry

Organism name Athyrium mesosorum
Genus Athyrium
Family Woodsiaceae / Dryopteridaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Athyrium
Linked NCBI taxonomy ID 32109
Linked level genus

Family

Family in NCBI taxonomy Athyriaceae
ID 1203520

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Euphyllophyta
ID 78536

Metabolite list (4)

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
C00002942 External link 512 Athyriol
No. 3 No. 15
C00002956 External link 512 Isoathyriol
No. 3 No. 15
C00002962 External link 512 Aphloiol
/ Mangiferin
/ 2-beta-D-Glucopyranosyl-1,3,6,7-tetrahydroxy xanthone
CHEMBL1329826
C013592
27 / 17 / 17 39 / 41 No. 22 No. 15
C00002968 External link 512 Norathyriol
/ 1,3,6,7-Tetrahydroxyxanthoene
CHEMBL187265
C069053
9 / 10 / 7 4 / 0 No. 71 No. 15

Human Protein / Gene in interactions

36 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002962 0 / 0
P29466 Caspase-1 C14 C00002962 0 / 0
P39900 Macrophage metalloelastase M10A C00002968 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00002968 2 / 2
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002962 0 / 0
Q9Y5X4 Photoreceptor-specific nuclear receptor NR2E3 C00002962 2 / 2
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002968 1 / 1
P49327 Fatty acid synthase Transferase C00002968 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002962 0 / 0
O75496 Geminin Unclassified protein C00002962 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002962 0 / 0
P03956 Interstitial collagenase M10A C00002968 0 / 1
Q9Y253 DNA polymerase eta Enzyme C00002962 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00002962 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00002962 3 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00002962 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002962 0 / 0
P45452 Collagenase 3 M10A C00002968 1 / 1
P10696 Alkaline phosphatase, placental-like Enzyme C00002962 0 / 1
P08253 72 kDa type IV collagenase M10A C00002968 1 / 3
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002962 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002962 2 / 2
P12821 Angiotensin-converting enzyme M2 C00002968 4 / 2
P55210 Caspase-7 C14 C00002962 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002962 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002962 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002962 0 / 0
P08254 Stromelysin-1 M10A C00002968 1 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002962 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002962 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002962 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00002962 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002962 1 / 4
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002962 5 / 3
Q9Y618 Nuclear receptor corepressor 2 Unclassified protein C00002962 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002962 0 / 0

41 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002962 C00002968
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00002962 C00002968
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00002962
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002962
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00002962
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002962
847 CAT catalase (EC:1.11.1.6) C00002962
891 CCNB1, CCNB cyclin B1 C00002962
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00002962
1147 CHUK, IKBKA, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16 conserved helix-loop-helix ubiquitous kinase (EC:2.7.11.10) C00002962
7852 CXCR4, CD184, D2S201E, FB22, HM89, HSY3RR, LAP3, LCR1, LESTR, NPY3R, NPYR, NPYRL, NPYY3R, WHIM chemokine (C-X-C motif) receptor 4 C00002962
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002962
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00002962
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00002962
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00002962
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00002962
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00002962
355 FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 Fas cell surface death receptor C00002962
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00002962
3551 IKBKB, IKK-beta, IKK2, IKKB, NFKBIKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta (EC:2.7.11.10) C00002962
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00002962
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002962
4023 LPL, HDLCQ11, LIPD lipoprotein lipase (EC:3.1.1.34) C00002962
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002962
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002962
4793 NFKBIB, IKBB, TRIP9 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, beta C00002962
4803 NGF, Beta-NGF, HSAN5, NGFB nerve growth factor (beta polypeptide) C00002962
5320 PLA2G2A, MOM1, PLA2, PLA2B, PLA2L, PLA2S, PLAS1, sPLA2 phospholipase A2, group IIA (platelets, synovial fluid) (EC:3.1.1.4) C00002962
25 ABL1, ABL, JTK7, bcr/abl, c-ABL, p150, v-abl c-abl oncogene 1, non-receptor tyrosine kinase (EC:2.7.10.2) C00002962
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002962
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002962
6716 SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2) (EC:1.3.1.22) C00002962
7015 TERT, CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT telomerase reverse transcriptase (EC:2.7.7.49) C00002962
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00002962
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002962
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002962
7364 UGT2B7, UDPGT_2B9, UDPGT2B7, UDPGTH2, UGT2B9 UDP glucuronosyltransferase 2 family, polypeptide B7 (EC:2.4.1.17) C00002962
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00002962
331 XIAP, API3, BIRC4, IAP-3, ILP1, MIHA, XLP2, hIAP-3, hIAP3 X-linked inhibitor of apoptosis C00002962
5467 PPARD, FAAR, NR1C2, NUC1, NUCI, NUCII, PPARB peroxisome proliferator-activated receptor delta C00002968
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00002968

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (27)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
%606641 Body mass index; bmi P37231
#300615 Brunner syndrome P21397
#609338 Carotid intimal medial thickness 1 P37231
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#119900 Digital clubbing, isolated congenital P15428
#268100 Enhanced s-cone syndrome; escs Q9Y5X4
#137800 Glioma susceptibility 1; glm1 P37231
#614519 Hemorrhage, intracerebral, susceptibility to; ich P12821
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#603932 Intervertebral disc disease; idd P14780
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#612624 Microvascular complications of diabetes, susceptibility to, 3; mvcd3 P12821
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#601665 Obesity P37231
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#267430 Renal tubular dysgenesis; rtd P12821
#611131 Retinitis pigmentosa 37; rp37 Q9Y5X4
#602111 Spondyloepimetaphyseal dysplasia, missouri type P45452
#601367 Stroke, ischemic P12821
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (24)

KEGG name UniProt
H00028 Choriocarcinoma P03956 (related)
P08253 (related)
H00213 Hypophosphatasia P05186 (related)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00023 Testicular cancer P10696 (marker)
H00083 Allograft rejection P12821 (related)
H00575 Renal tubular dysgenesis P12821 (related)
H00479 Metaphyseal dysplasias P14780 (related)
P45452 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00548 Brunner syndrome P21397 (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) 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)
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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)
H00527 Retinitis pigmentosa (RP) Q9Y5X4 (related)
H00805 Vitreoretinal degeneration Q9Y5X4 (related)

Diseases related to CTD interactions

41 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D016301 Alveolar Bone Loss C00002962
D000707 Anaphylaxis C00002962
D050197 Atherosclerosis C00002962
D001847 Bone Diseases C00002962
D001862 Bone Resorption C00002962
D003248 Constipation C00002962
D003457 Cryptosporidiosis C00002962
D003921 Diabetes Mellitus, Experimental C00002962
D003924 Diabetes Mellitus, Type 2 C00002962
D003928 Diabetic Nephropathies C00002962
D056486 Drug-Induced Liver Injury C00002962
D005234 Fatty Liver C00002962
D006331 Heart Diseases C00002962
D006561 Herpes Simplex C00002962
D015658 HIV Infections C00002962
D006946 Hyperinsulinism C00002962
D006949 Hyperlipidemias C00002962
D006967 Hypersensitivity C00002962
D033461 Hyperuricemia C00002962
D007154 Immune System Diseases C00002962
D007249 Inflammation C00002962
D007333 Insulin Resistance C00002962
D007511 Ischemia C00002962
D007674 Kidney Diseases C00002962
D007859 Learning Disorders C00002962
D015464 Leukemia, Myelogenous, Chronic, BCR-ABL Positive C00002962
D015470 Leukemia, Myeloid, Acute C00002962
D008175 Lung Neoplasms C00002962
D008569 Memory Disorders C00002962
D008630 Mercury Poisoning C00002962
D009203 Myocardial Infarction C00002962
D009336 Necrosis C00002962
D009410 Nerve Degeneration C00002962
D009437 Neuralgia C00002962
D010300 Parkinson Disease C00002962
D010518 Periodontitis C00002962
D011470 Prostatic Hyperplasia C00002962
D011833 Radiation Injuries, Experimental C00002962
D012772 Shock, Septic C00002962
D013276 Stomach Ulcer C00002962
D014235 Trichinellosis C00002962