| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YHR204W | MNL1 | SGDID:S000001247 | Caul_4035 |
Caul_4035 |
3.2.1.113 | Caulobacter | 4ayo_a | B0SWV2 | 100.00 | 4.00E-109 | 4.00E-113 | 929.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR204W | MNL1 | SGDID:S000001247 | MDS1 |
MDS1 |
3.2.1.-,3.2.1.113, | Hypocrea jecorina | 1hcu_b | Q9P8T8 | 100.00 | 5.00E-106 | 4.00E-110 | 916.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR204W | MNL1 | SGDID:S000001247 | MSDC |
Mannosyl-oligosaccharide alpha-1,2-mannosidase (EC 3.2.1.113) (Man(9)-alpha-mannosidase) |
3.2.1.113 | Penicillium citrinum | 2ri8_b | P31723 | 100.00 | 1.00E-108 | 1.00E-112 | 932.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR204W | MNL1 | SGDID:S000001247 | MDS1 |
alpha-1,2-Mannosidase (EC 3.2.1.-) |
3.2.1.-,3.2.1.113, | Hypocrea jecorina | 1hcu_a | Q9P8T8 | 100.00 | 4.00E-119 | 3.00E-123 | 1019.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR204W | MNL1 | SGDID:S000001247 | MAN1B1 UNQ747/PRO1477 |
Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase (EC 3.2.1.113) (ER alpha-1,2-mannosidase) (ER mannosidase 1) (ERMan1) (Man9GlcNAc2-specific-processing alpha-mannosidase) (Mannosidase alpha class 1B member 1) |
3.2.1.113 | Homo sapiens | Man1b1-Cdg,Anemia, Congenital Dyserythropoietic, Type Iii,Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome,Alpha-1-Antitrypsin Deficiency,Congenital Disorder Of Glycosylation, Type Iif,Fructose Intolerance, Hereditary,Congenital Disorder Of Glycosylation, Type Iim,Rafiq Syndrome,Congenital Disorder Of Glycosylation, Type Iib,Immunodeficiency 47,Congenital Disorder Of Glycosylation, Type In,Mannosidosis, Alpha B, Lysosomal,Congenital Disorder Of Glycosylation, Type Iik,Congenital Disorder Of Glycosylation, Type Iio,Congenital Disorder Of Glycosylation, Type Iip,Autosomal Recessive Non-Syndromic Intellectual Disability |
1x9d_a | Q9UKM7 | ENSG00000177239 | MAN1B1 | 100.00 | 6.00E-110 | 5.00E-114 | 953.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YHR204W | MNL1 | SGDID:S000001247 | Man1a1 Man1a |
Mannosyl-oligosaccharide 1,2-alpha-mannosidase IA (EC 3.2.1.113) (Man(9)-alpha-mannosidase) (Man9-mannosidase) (Mannosidase alpha class 1A member 1) (Processing alpha-1,2-mannosidase IA) (Alpha-1,2-mannosidase IA) |
3.2.1.113 | Mus musculus | 5kkb_a | P45700 | 100.00 | 5.00E-107 | 4.00E-111 | 917.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 |