| Organism name | Cryptocarya longifolia Kostermans | 
|---|---|
| Genus | Cryptocarya | 
| Family | Lauraceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Cryptocarya | 
|---|---|
| Linked NCBI taxonomy ID | 22027 | 
| Linked level | genus | 
| Family in NCBI taxonomy | Lauraceae | 
|---|---|
| ID | 3433 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | Magnoliophyta | 
|---|---|
| ID | 3398 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00025397   | Rotundine / (-)-Bisnorargemonine | CHEMBL518908 CHEMBL1494954 | 1 / 0 / 0 | No. 37 | No. 4 |   | ||
| C00025402   | Norargemonine / (-)-Norargemonine / O2-Demetylargemonie / O8-Demethylargemonine | CHEMBL1570385 | 2 / 2 / 0 | No. 37 | No. 4 |   | ||
| C00026092   | Scoulerine / (-)-Scoulerine | CHEMBL191133 CHEMBL1235966 CHEMBL1395394 | 27 / 19 / 15 | No. 37 | No. 4 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| O75496 | Geminin | Unclassified protein | C00025402 C00026092 | 0 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00026092 | 0 / 0 | 
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00026092 | 0 / 0 | 
| P29466 | Caspase-1 | C14 | C00026092 | 0 / 0 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00026092 | 11 / 10 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00026092 | 0 / 1 | 
| P14416 | D(2) dopamine receptor | Dopamine receptor | C00026092 | 2 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00026092 | 0 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00025402 | 2 / 0 | 
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00026092 | 1 / 0 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00026092 | 0 / 0 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00026092 | 1 / 1 | 
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00026092 | 0 / 0 | 
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00026092 | 0 / 0 | 
| Q99700 | Ataxin-2 | Unclassified protein | C00026092 | 1 / 1 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00026092 | 0 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00026092 | 0 / 0 | 
| P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00026092 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00026092 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00026092 | 0 / 1 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00026092 | 0 / 0 | 
| O14727 | Apoptotic protease-activating factor 1 | Unclassified protein | C00026092 | 0 / 0 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00026092 | 0 / 0 | 
| P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00026092 | 1 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00026092 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00026092 | 0 / 0 | 
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00026092 | 1 / 0 | 
| Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00026092 | 0 / 0 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00025397 | 0 / 0 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #103780 | Alcohol dependence | P14416 | 
| #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 | 
| #137800 | Glioma susceptibility 1; glm1 | O75874 | 
| #610140 | Heart-hand syndrome, slovenian type | P02545 | 
| #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 | 
| #159900 | Myoclonic dystonia | P14416 | 
| #614674 | Periodic fever, menstrual cycle-dependent | P08908 | 
| #275210 | Restrictive dermopathy, lethal | P02545 | 
| #183090 | Spinocerebellar ataxia 2; sca2 | Q99700 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| 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) | 
| H01205 | Coumarin resistance | P11712
                            (related) | 
| H01171 | Poor drug metabolism (PM) | P33261
                            (related) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q99700
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |