| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YML056C | IMD4 | SGDID:S000004520 | IMD1 |
IMD1 |
1.1.1.205 | Cryptococcus neoformans | 4af0_b | E3P6S0 | 100.00 | 1.80E-38 | 1.30E-42 | 335.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YML056C | IMD4 | SGDID:S000004520 | AGOS_AER117W |
AGOS_AER117W |
1.1.1.205 | Ashbya gossypii | 4z87_b | Q756Z6 | 99.90 | 9.20E-32 | 6.70E-36 | 282.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YML056C | IMD4 | SGDID:S000004520 | IMPDH2 IMPD2 |
Inosine-5'-monophosphate dehydrogenase 2 (IMP dehydrogenase 2) (IMPD 2) (IMPDH 2) (EC 1.1.1.205) (IMPDH-II) |
1.1.1.205 | Homo sapiens | Retinitis Pigmentosa,Impdh2 Enzyme Activity, Variation In |
1nf7_a | P12268 | ENSG00000178035 | IMPDH2 | 99.90 | 1.10E-29 | 7.90E-34 | 265.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YML056C | IMD4 | SGDID:S000004520 | guaB PA3770 |
guaB PA3770 |
1.1.1.205 | Pseudomonas aeruginosa | 5ahn_a | Q9HXM5 | 99.90 | 4.70E-30 | 3.40E-34 | 267.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YML056C | IMD4 | SGDID:S000004520 | IMPDH1 IMPD1 |
Inosine-5'-monophosphate dehydrogenase 1 (IMP dehydrogenase 1) (IMPD 1) (IMPDH 1) (EC 1.1.1.205) (IMPDH-I) |
1.1.1.205 | Homo sapiens | Senior-Loken Syndrome 1,Retinitis Pigmentosa,Pseudoretinitis Pigmentosa,Leber Congenital Amaurosis 9,Pathologic Nystagmus,Eye Degenerative Disease,Leber Plus Disease,Retinal Degeneration,Fundus Dystrophy,Keratoconus,Retinal Disease,Usher Syndrome, Type I,Usher Syndrome, Type Iiia,Stargardt Disease,Cone-Rod Dystrophy 2,Retinitis,Leber Congenital Amaurosis 3,Retinitis Pigmentosa 1,Retinitis Pigmentosa 9,Retinitis Pigmentosa 10,Leber Congenital Amaurosis 6,Leber Congenital Amaurosis 7,Leber Congenital Amaurosis 8,Leber Congenital Amaurosis 11,Leber Congenital Amaurosis 15,Leber Congenital Amaurosis 4,Usher Syndrome,Osteopetrosis, Autosomal Recessive 4,Osteopetrosis, Autosomal Recessive 6,Leber Congenital Amaurosis 16,Leber Congenital Amaurosis 10,Osteopetrosis, Autosomal Recessive 7,Leber Congenital Amaurosis 1,Leber Congenital Amaurosis 2,Osteopetrosis, Autosomal Recessive 1,Joubert Syndrome 1,Osteopetrosis, Autosomal Recessive 5 |
1jcn_b | P20839 | ENSG00000106348 | IMPDH1 | 99.90 | 1.30E-30 | 9.60E-35 | 272.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |