| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YOR335C | ALA1 | SGDID:S000005862 | tRNA-synt_2c |
tRNA synthetases class II (A) |
pfam Family | PF01411 | 100.00 | 1.20E-94 | 9.00E-99 | 849.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YOR335C | ALA1 | SGDID:S000005862 | alaS AF_2255 |
Alanine--tRNA ligase (EC 6.1.1.7) (Alanyl-tRNA synthetase) (AlaRS) |
6.1.1.7 | Archaeoglobus fulgidus | 2ztg_a | O28029 | 100.00 | 9.00E-123 | 6.00E-127 | 1110.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOR335C | ALA1 | SGDID:S000005862 | alaS PH0297 |
Alanine--tRNA ligase (EC 6.1.1.7) (Alanyl-tRNA synthetase) (AlaRS) |
6.1.1.7 | Pyrococcus horikoshii | 2zze_a | O58035 | 100.00 | 6.00E-128 | 4.00E-132 | 1155.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOR335C | ALA1 | SGDID:S000005862 | alaS aq_1293 |
Alanine--tRNA ligase (EC 6.1.1.7) (Alanyl-tRNA synthetase) (AlaRS) |
6.1.1.7 | Aquifex aeolicus | 1yfs_b | O67323 | 100.00 | 4.20E-99 | 3.00E-103 | 860.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOR335C | ALA1 | SGDID:S000005862 | alaS lovB b2697 JW2667 |
Alanine--tRNA ligase (EC 6.1.1.7) (Alanyl-tRNA synthetase) (AlaRS) |
6.1.1.7 | Escherichia coli | 3hxx_a | P00957 | 100.00 | 1.40E-99 | 1.00E-103 | 860.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
| YOR335C | ALA1 | SGDID:S000005862 | AARS1 AARS |
Alanine--tRNA ligase, cytoplasmic (EC 6.1.1.7) (Alanyl-tRNA synthetase) (AlaRS) (Renal carcinoma antigen NY-REN-42) |
6.1.1.7 | Homo sapiens | Robinow Syndrome, Autosomal Recessive 1,Clubfoot,Charcot-Marie-Tooth Disease, Dominant Intermediate C,Neuromuscular Disease,Infantile Liver Failure Syndrome,Combined Oxidative Phosphorylation Deficiency 12,Myositis,Undetermined Early-Onset Epileptic Encephalopathy,Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease, Axonal, Type 2d,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Trichohepatoenteric Syndrome 1,Charcot-Marie-Tooth Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2n,Microcephaly,Tooth Disease,Cataract 4, Multiple Types,Rigid Spine Muscular Dystrophy 1,Charcot-Marie-Tooth Disease, Axonal, Type 2a1,Charcot-Marie-Tooth Disease And Deafness,Charcot-Marie-Tooth Disease, Recessive Intermediate B,Microphthalmia, Syndromic 5,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Charcot-Marie-Tooth Disease, Axonal, Type 2b2,Pontocerebellar Hypoplasia, Type 6,Charcot-Marie-Tooth Disease Intermediate Type,Charcot-Marie-Tooth Disease, Axonal, Type 2u,Developmental And Epileptic Encephalopathy 29,Perrault Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2i,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Mitochondrial Dna Depletion Syndrome 4a,Neuronopathy, Distal Hereditary Motor, Type Va |
4xem_a | P49588 | ENSG00000090861 | AARS1 | 100.00 | 2.00E-108 | 1.00E-112 | 935.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |