| Organism name | Berberis sibirica | 
|---|---|
| Genus | Berberis | 
| Family | Berberidaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Berberis | 
|---|---|
| Linked NCBI taxonomy ID | 22774 | 
| Linked level | genus | 
| Family in NCBI taxonomy | Berberidaceae | 
|---|---|
| ID | 41773 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | eudicotyledons | 
|---|---|
| ID | 71240 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00001817   | Berbamine / d-Berbamine / (+)-Berbamine | CHEMBL504323 CHEMBL507540 CHEMBL1198334 | C027870 | 4 / 3 / 4 | 9 / 1 | No. 10 | No. 4 |   | 
| C00001897   | Oxyacanthine | CHEMBL510022 CHEMBL509999 CHEMBL1983122 | C092646 | 5 / 4 / 1 | No. 10 | No. 4 |   | |
| C00025266   | Isosinomenin A / Isotetrandrine / Isosinomenine A / O-Methylberbamine / (+)-Isotetrandrine / O,O-Dimethylobamegine / O,O'-Dimethylobamegine / O,O-Dimethylstepholine / O,O'-Dimethylstepholine | No. 10 | No. 4 |   | ||||
| C00001905   | Milthanthine / Pronuciferine / (+)-Pronuciferine / N-Methylstepharine / N,O-Dimethylcrotonosine | CHEMBL237766 | No. 688 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q99700 | Ataxin-2 | Unclassified protein | C00001897 | 1 / 1 | 
| P54750 | Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A | PDE_1A | C00001817 | 0 / 0 | 
| O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00001817 | 0 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00001897 | 2 / 0 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001817 | 3 / 3 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001817 | 0 / 1 | 
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00001897 | 0 / 0 | 
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001897 | 1 / 0 | 
| P43351 | DNA repair protein RAD52 homolog | Unclassified protein | C00001897 | 0 / 0 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 598 | BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS | BCL2-like 1 | C00001817 | 
| 637 | BID, FP497 | BH3 interacting domain death agonist | C00001817 | 
| 332 | BIRC5, API4, EPR-1 | baculoviral IAP repeat containing 5 | C00001817 | 
| 836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) | C00001817 | 
| 595 | CCND1, BCL1, D11S287E, PRAD1, U21B31 | cyclin D1 | C00001817 | 
| 1147 | CHUK, IKBKA, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16 | conserved helix-loop-helix ubiquitous kinase (EC:2.7.11.10) | C00001817 | 
| 4792 | NFKBIA, IKBA, MAD-3, NFKBI | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha | C00001817 | 
| 5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A | C00001817 | 
| 7128 | TNFAIP3, A20, OTUD7C, TNFA1P2 | tumor necrosis factor, alpha-induced protein 3 (EC:3.4.19.12) | C00001817 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | Q99714 | 
| #114500 | Colorectal cancer; crc | P84022 | 
| #137800 | Glioma susceptibility 1; glm1 | O75874 | 
| #613795 | Loeys-dietz syndrome, type 3; lds3 | P84022 | 
| #300705 | Mental retardation, x-linked 17; mrx17 | Q99714 | 
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 | Q99714 | 
| #183090 | Spinocerebellar ataxia 2; sca2 | Q99700 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q99700
                            (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) |