Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YDR452W | PPN1 | SGDID:S000002860 | cpdA ph |
cpdA ph |
3.1.4.53 | Klebsiella aerogenes | 3d03_a | Q6XBH1 | 99.30 | 2.40E-16 | 2.60E-20 | 151.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR452W | PPN1 | SGDID:S000002860 | Smpdl3a Asml3a |
Acid sphingomyelinase-like phosphodiesterase 3a (ASM-like phosphodiesterase 3a) (EC 3.1.4.-) |
3.1.4.- | Mus musculus | 5fc1_a | P70158 | 99.90 | 6.10E-31 | 6.10E-35 | 279.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR452W | PPN1 | SGDID:S000002860 | SMPD1 ASM |
Sphingomyelin phosphodiesterase (EC 3.1.4.12) (Acid sphingomyelinase) (aSMase) |
3.1.4.12 | Homo sapiens | Lysosomal And Lipase Deficiency,Mucolipidosis,Gaucher'S Disease,Sphingolipidosis,Lipid Storage Disease,Sandhoff Disease,Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy,Aggressive Systemic Mastocytosis,Cystic Fibrosis,Acid Sphingomyelinase Deficiency,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Mucopolysaccharidosis Iv,Ceroid Lipofuscinosis, Neuronal, 6,Acquired Hyperkeratosis,Tay-Sachs Disease,Nephrotic Syndrome, Type 14,Cerebral Lipidosis,Lysosomal Storage Disease,Pick Disease Of Brain,Lysosomal Acid Lipase Deficiency,Gm2 Gangliosidosis,Alacrima, Achalasia, And Mental Retardation Syndrome,Gm1 Gangliosidosis,Neuronal Ceroid Lipofuscinosis,Niemann-Pick Disease,Farber Lipogranulomatosis,Disease Of Mental Health,Gm1-Gangliosidosis, Type I,Gaucher Disease, Type I,Beckwith-Wiedemann Syndrome,Krabbe Disease,Metachromatic Leukodystrophy,Niemann-Pick Disease, Type B,Niemann-Pick Disease, Type C2,Mucolipidosis Ii Alpha/Beta,Ceroid Lipofuscinosis, Neuronal, 3,Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive,C Syndrome,Niemann-Pick Disease, Type A,Niemann-Pick Disease, Type C1 |
5i81_a | P17405 | ENSG00000166311 | SMPD1 | 99.90 | 8.40E-32 | 7.90E-36 | 301.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR452W | PPN1 | SGDID:S000002860 | lmo2642 |
lmo2642 |
Listeria monocytogenes | 2xmo_b | Q8Y432 | 99.30 | 1.60E-16 | 1.70E-20 | 166.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR452W | PPN1 | SGDID:S000002860 | ACP5 |
Tartrate-resistant acid phosphatase type 5 (TR-AP) (EC 3.1.3.2) (Tartrate-resistant acid ATPase) (TrATPase) (Type 5 acid phosphatase) (Uteroferrin) (UF) |
3.1.3.2 | Sus scrofa | 1ute_a | P09889 | 99.20 | 7.40E-16 | 7.70E-20 | 152.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR452W | PPN1 | SGDID:S000002860 | adprm zgc:64213 |
Manganese-dependent ADP-ribose/CDP-alcohol diphosphatase (EC 3.6.1.13) (EC 3.6.1.16) (EC 3.6.1.53) (ADPRibase-Mn) (CDP-choline phosphohydrolase) |
3.6.1.13,3.6.1.16,3.6.1.53 | Danio rerio | 2nxf_a | Q7T291 | 99.20 | 7.20E-16 | 7.80E-20 | 151.50 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | |||
YDR452W | PPN1 | SGDID:S000002860 | Smpd1 Asm |
Sphingomyelin phosphodiesterase (EC 3.1.4.12) (Acid sphingomyelinase) (ASMase) |
3.1.4.12 | Mus musculus | 5fib_b | Q04519 | 99.90 | 4.00E-32 | 3.80E-36 | 300.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR452W | PPN1 | SGDID:S000002860 | Smpdl3b Asml3b |
Acid sphingomyelinase-like phosphodiesterase 3b (ASM-like phosphodiesterase 3b) (EC 3.1.4.-) |
3.1.4.- | Mus musculus | 5kar_a | P58242 | 99.90 | 2.00E-30 | 2.00E-34 | 274.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR452W | PPN1 | SGDID:S000002860 | SMPDL3A ASML3A |
Acid sphingomyelinase-like phosphodiesterase 3a (ASM-like phosphodiesterase 3a) (EC 3.1.4.-) |
3.1.4.- | Homo sapiens | 5ebb_a | Q92484 | ENSG00000172594 | SMPDL3A | 99.90 | 2.70E-32 | 2.80E-36 | 287.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR452W | PPN1 | SGDID:S000002860 | ACP5 |
Tartrate-resistant acid phosphatase type 5 (TR-AP) (EC 3.1.3.2) (Tartrate-resistant acid ATPase) (TrATPase) (Type 5 acid phosphatase) |
3.1.3.2 | Homo sapiens | Bone Disease,Bone Remodeling Disease,Ischemic Bone Disease,Bone Resorption Disease,Metaphyseal Dysplasia,Bone Giant Cell Tumor,Connective Tissue Disease,Gaucher'S Disease,Teeth Hard Tissue Disease,Diamond-Blackfan Anemia 1,Sjogren-Larsson Syndrome,Villonodular Synovitis,Secondary Hyperparathyroidism,Chronic Kidney Disease,Hyperthyroidism,Epiglottis Cancer,Periapical Periodontitis,Periodontitis,Osteopetrosis, Autosomal Recessive 8,Nodular Tenosynovitis,Pigmented Villonodular Synovitis,Synovitis,Arthritis,Renal Osteodystrophy,Osteonecrosis,Osteomyelitis,Enchondromatosis, Multiple, Ollier Type,Tooth Resorption,Paget'S Disease Of Bone,Hairy Cell Leukemia,Osteopetrosis, Autosomal Dominant 2,Osteoporosis,Femoral Cancer,Osteopetrosis,Hyperparathyroidism,Malignant Giant Cell Tumor Of Soft Parts,Microphthalmia,Hemiplegia,Bone Inflammation Disease,Parathyroid Gland Disease,Tendinitis,Mammary Paget'S Disease,Brittle Bone Disorder,Craniometaphyseal Dysplasia, Autosomal Dominant,Rheumatoid Arthritis,Congenital Hypothyroidism,Camurati-Engelmann Disease,Odontochondrodysplasia,Endosteal Hyperostosis, Autosomal Dominant,Acid Phosphatase Deficiency,Bone Benign Neoplasm,Scoliosis,Leukemia, Chronic Lymphocytic,Spondyloenchondrodysplasia With Immune Dysregulation,Glucocorticoid-Induced Osteoporosis,Myelofibrosis,Osteopetrosis, Autosomal Recessive 2,Pycnodysostosis |
1war_a | P13686 | ENSG00000102575 | ACP5 | 99.10 | 5.50E-15 | 6.10E-19 | 142.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR452W | PPN1 | SGDID:S000002860 | PF3D7_0918000 |
PF3D7_0918000 |
3.1.3.2 | Plasmodium falciparum | 3tgh_a | Q8I2X3 | 99.10 | 6.30E-15 | 6.70E-19 | 147.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |