| class name | count | 
|---|---|
| rosids | 11 | 
| class name | count | 
|---|---|
| Phyllanthaceae | 10 | 
| Polygalaceae | 1 | 
| br08003 Category | # of metabolite | 
|---|
| br08003 Category | KEGG ID | KNApSAcK 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  | 
                      figure | 
|---|---|---|---|---|---|---|
| 
                        C00002360
                        
                           | 
                      
                        Securinine
                         | 
                      
                        CHEMBL303062
                         CHEMBL1355372 CHEMBL1358404 CHEMBL1495075 CHEMBL1529147 CHEMBL1965517  | 
                      
                        C000785
                         | 
                      19 / 26 / 19 | 
                         
                       | 
                    |
| 
                        C00026161
                        
                           | 
                      
                        4-Methoxynorsecurinine
                         | 
                      
                         
                       | 
                    ||||
| 
                        C00038167
                        
                           | 
                      
                        15alpha-Methoxy-14,15-dihydrophyllochrysine
                         | 
                      
                        CHEMBL398307
                         | 
                      
                         
                       | 
                    |||
| 
                        C00038277
                        
                           | 
                      
                        4-Epiphyllanthine
                         | 
                      
                         
                       | 
                    ||||
| 
                        C00039994
                        
                           | 
                      
                        Phyllantidine
                         / (-)-Phyllantidine  | 
                      
                        CHEMBL398499
                         | 
                      
                         
                       | 
                    |||
| 
                        C00040270
                        
                           | 
                      
                        Securitinine
                         | 
                      
                         
                       | 
                    
| accession | description | class description | KNApSAcK metabolite in interactions | 
                          # of diseases
                           (OMIM / KEGG)  | 
                      
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002360 | 1 / 0 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00002360 | 4 / 1 | 
| Q99700 | Ataxin-2 | Unclassified protein | C00002360 | 1 / 1 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00002360 | 11 / 10 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002360 | 0 / 1 | 
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002360 | 1 / 0 | 
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00002360 | 0 / 0 | 
| P42858 | Huntingtin | Unclassified protein | C00002360 | 1 / 1 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002360 | 2 / 0 | 
| O75496 | Geminin | Unclassified protein | C00002360 | 0 / 0 | 
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00002360 | 0 / 0 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002360 | 0 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002360 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002360 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002360 | 0 / 1 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00002360 | 4 / 3 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002360 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002360 | 0 / 0 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002360 | 0 / 0 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a | 
                            P02545
                             | 
                        
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism | 
                            P02545
                             | 
                        
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 | 
                            P02545
                             | 
                        
| #114500 | Colorectal cancer; crc | 
                            P84022
                             | 
                        
| #609535 | Drug metabolism, poor, cyp2c19-related | 
                            P33261
                             | 
                        
| #608902 | Drug metabolism, poor, cyp2d6-related | 
                            P10635
                             | 
                        
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | 
                            P02545
                             | 
                        
| #600274 | Frontotemporal dementia; ftd | 
                            P10636
                             | 
                        
| #610140 | Heart-hand syndrome, slovenian type | 
                            P02545
                             | 
                        
| #143100 | Huntington disease; hd | 
                            P42858
                             | 
                        
| #176670 | Hutchinson-gilford progeria syndrome; hgps | 
                            P02545
                             | 
                        
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 | 
                            P02545
                             | 
                        
| #613795 | Loeys-dietz syndrome, type 3; lds3 | 
                            P84022
                             | 
                        
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada | 
                            P02545
                             | 
                        
| #613205 | Muscular dystrophy, congenital, lmna-related | 
                            P02545
                             | 
                        
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b | 
                            P02545
                             | 
                        
| #160900 | Myotonic dystrophy 1; dm1 | 
                            Q9NR56
                             | 
                        
| #260540 | Parkinson-dementia syndrome | 
                            P10636
                             | 
                        
| #172700 | Pick disease of brain | 
                            P10636
                             | 
                        
| #275210 | Restrictive dermopathy, lethal | 
                            P02545
                             | 
                        
| #253300 | Spinal muscular atrophy, type i; sma1 | 
                            Q16637
                             | 
                        
| #253550 | Spinal muscular atrophy, type ii; sma2 | 
                            Q16637
                             | 
                        
| #253400 | Spinal muscular atrophy, type iii; sma3 | 
                            Q16637
                             | 
                        
| #271150 | Spinal muscular atrophy, type iv; sma4 | 
                            Q16637
                             | 
                        
| #183090 | Spinocerebellar ataxia 2; sca2 | 
                            Q99700
                             | 
                        
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | 
                            P10636
                             | 
                        
| KEGG | name | UniProt | 
|---|---|---|
| H00264 | Charcot-Marie-Tooth disease (CMT) | 
                            P02545
                            (related)
                             | 
                        
| H00294 | Dilated cardiomyopathy (DCM) | 
                            P02545
                            (related)
                             | 
                        
| H00420 | Familial partial lipodystrophy (FPL) | 
                            P02545
                            (related)
                             | 
                        
| H00563 | Emery-Dreifuss muscular dystrophy | 
                            P02545
                            (related)
                             | 
                        
| H00590 | Congenital muscular dystrophies (CMD/MDC) | 
                            P02545
                            (related)
                             | 
                        
| H00593 | Limb-girdle muscular dystrophy (LGMD) | 
                            P02545
                            (related)
                             | 
                        
| H00601 | Hutchinson-Gilford progeria syndrome | 
                            P02545
                            (related)
                             | 
                        
| H00663 | Restrictive dermopathy | 
                            P02545
                            (related)
                             | 
                        
| H00665 | Mandibuloacral dysplasia | 
                            P02545
                            (related)
                             | 
                        
| H01216 | Left ventricular noncompaction (LVNC) | 
                            P02545
                            (related)
                             | 
                        
| H00036 | Osteosarcoma | 
                            P08684
                            (marker)
                             | 
                        
| H00058 | Amyotrophic lateral sclerosis (ALS) | 
                            P10636
                            (related)
                             | 
                        
| H00077 | Progressive supranuclear palsy (PSP) | 
                            P10636
                            (related)
                             | 
                        
| H00078 | Frontotemporal lobar degeneration (FTLD) | 
                            P10636
                            (related)
                             | 
                        
| H01205 | Coumarin resistance | 
                            P11712
                            (related)
                             | 
                        
| H01171 | Poor drug metabolism (PM) | 
                            P33261
                            (related)
                             | 
                        
| H00059 | Huntington's disease (HD) | 
                            P42858
                            (related)
                             | 
                        
| H00455 | Spinal muscular atrophy (SMA) | 
                            Q16637
                            (related)
                             | 
                        
| H00063 | Spinocerebellar ataxia (SCA) | 
                            Q99700
                            (related)
                             |