| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YOL095C | HMI1 | SGDID:S000005455 | uvrD mutU pdeB rad recL b3813 JW3786 |
DNA helicase II (EC 3.6.4.12) |
3.6.4.12 | Escherichia coli | 3lfu_a | P03018 | 99.80 | 3.70E-24 | 3.00E-28 | 244.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
| YOL095C | HMI1 | SGDID:S000005455 | DR_1775 |
DR_1775 |
3.6.4.12 | Deinococcus radiodurans | 4c2u_a | Q9RTI9 | 99.80 | 5.00E-25 | 4.00E-29 | 252.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOL095C | HMI1 | SGDID:S000005455 | IGHMBP2 SMBP2 SMUBP2 |
DNA-binding protein SMUBP-2 (EC 3.6.4.12) (EC 3.6.4.13) (ATP-dependent helicase IGHMBP2) (Glial factor 1) (GF-1) (Immunoglobulin mu-binding protein 2) |
3.6.4.13 | Homo sapiens | Spinal Muscular Atrophy With Lower Extremity Predominance,Adult Respiratory Distress Syndrome,Myopathy,Progressive Multifocal Leukoencephalopathy,Neuromuscular Disease,Amyotrophic Lateral Sclerosis 1,Neuronopathy, Distal Hereditary Motor, Type Iib,Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease Type 2a2a,Muscular Atrophy,Anterior Horn Cell Disease,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Distal Hereditary Motor Neuronopathy Type 2,Motor Peripheral Neuropathy,Charcot-Marie-Tooth Hereditary Neuropathy,Diaphragmatic Eventration,Neuropathy,Charcot-Marie-Tooth Disease,Amyotrophic Lateral Sclerosis 4, Juvenile,Polyneuropathy,Neonatal Myasthenia Gravis,Autosomal Dominant Intermediate Charcot-Marie-Tooth,Tooth Disease,Respiratory Failure,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1,Scapuloperoneal Spinal Muscular Atrophy,Brown-Vialetto-Van Laere Syndrome,Spinal Muscular Atrophy, X-Linked 2,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Childhood Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Ptosis,Spinal Muscular Atrophy, Type I,Spinal Muscular Atrophy, Type Iii,Spinal Muscular Atrophy, Type Ii,Charcot-Marie-Tooth Disease, Axonal, Type 2t,Neuronopathy, Distal Hereditary Motor, Type Va |
4b3f_x | P38935 | ENSG00000132740 | IGHMBP2 | 99.40 | 1.10E-17 | 8.80E-22 | 191.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOL095C | HMI1 | SGDID:S000005455 | addA BSU10630 |
ATP-dependent helicase/nuclease subunit A (EC 3.1.-.-) (EC 3.6.4.12) (ATP-dependent helicase/nuclease AddA) |
3.1.-.-,3.6.4.12, | Bacillus subtilis | 3u4q_a | P23478 | 99.80 | 5.80E-24 | 4.60E-28 | 261.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOL095C | HMI1 | SGDID:S000005455 | recB ior rorA b2820 JW2788 |
RecBCD enzyme subunit RecB (EC 3.1.11.5) (Exodeoxyribonuclease V 135 kDa polypeptide) (Exodeoxyribonuclease V beta chain) (Exonuclease V subunit RecB) (ExoV subunit RecB) (Helicase/nuclease RecBCD subunit RecB) |
3.1.11.5 | Escherichia coli | 1w36_b | P08394 | 99.70 | 4.00E-23 | 3.20E-27 | 252.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
| YOL095C | HMI1 | SGDID:S000005455 | AQR KIAA0560 |
RNA helicase aquarius (EC 3.6.4.13) (Intron-binding protein of 160 kDa) (IBP160) |
3.6.4.13 | Homo sapiens | Robinow Syndrome, Autosomal Recessive 1,Retinitis Pigmentosa 26,Noonan Syndrome 1,Retinitis Pigmentosa 22,Histiocytosis-Lymphadenopathy Plus Syndrome,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Acrofacial Dysostosis,Acrofacial Dysostosis 1, Nager Type,Retinitis Pigmentosa 14 |
4pj3_a | O60306 | ENSG00000021776 | AQR | 99.40 | 6.10E-17 | 4.50E-21 | 198.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOL095C | HMI1 | SGDID:S000005455 | UPF1 KIAA0221 RENT1 |
Regulator of nonsense transcripts 1 (EC 3.6.4.-) (ATP-dependent helicase RENT1) (Nonsense mRNA reducing factor 1) (NORF1) (Up-frameshift suppressor 1 homolog) (hUpf1) |
3.6.4.- | Homo sapiens | Spinal Muscular Atrophy,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Long Qt Syndrome,Waardenburg Syndrome, Type 4b,Pancreatic Adenosquamous Carcinoma,Amyotrophic Lateral Sclerosis 4, Juvenile,Waardenburg Syndrome, Type 4a,Epidermolysis Bullosa, Junctional, Non-Herlitz Type,Disease Of Mental Health,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1,Coffin-Siris Syndrome 1,Choroideremia,Atrial Septal Defect 2,Ullrich Congenital Muscular Dystrophy 1 |
2xzo_a | Q92900 | ENSG00000005007 | UPF1 | 99.40 | 1.50E-17 | 1.20E-21 | 189.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOL095C | HMI1 | SGDID:S000005455 | NAM7 IFS2 MOF4 UPF1 YMR080C YM9582.05C |
ATP-dependent helicase NAM7 (EC 3.6.4.-) (Nonsense-mediated mRNA decay protein 1) (Nuclear accommodation of mitochondria 7 protein) (Up-frameshift suppressor 1) |
3.6.4.- | Saccharomyces cerevisiae | 2xzl_a | P30771 | 99.40 | 7.00E-17 | 5.30E-21 | 188.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOL095C | HMI1 | SGDID:S000005455 | rep b3778 JW5604 |
ATP-dependent DNA helicase Rep (EC 3.6.4.12) |
3.6.4.12 | Escherichia coli | 1uaa_a | P09980 | 99.90 | 4.80E-27 | 3.80E-31 | 270.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |