| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YFR053C | HXK1 | SGDID:S000001949 | HXK1 GIN2 At4g29130 F19B15.160 |
Hexokinase-1 (EC 2.7.1.1) (Protein GLUCOSE INSENSITIVE 2) |
2.7.1.1 | Arabidopsis thaliana | 4qs7_a | Q42525 | 100.00 | 1.20E-42 | 8.40E-47 | 346.60 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YFR053C | HXK1 | SGDID:S000001949 | HK3 |
Hexokinase-3 (EC 2.7.1.1) (Hexokinase type III) (HK III) (Hexokinase-C) |
2.7.1.1 | Homo sapiens | 3hm8_a | P52790 | ENSG00000160883 | HK3 | 100.00 | 1.20E-41 | 7.90E-46 | 336.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YFR053C | HXK1 | SGDID:S000001949 | RAG5 KLLA0D11352g |
Hexokinase (EC 2.7.1.1) |
2.7.1.1 | Kluyveromyces lactis | 3o4w_a | P33284 | 100.00 | 2.00E-57 | 1.40E-61 | 454.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YFR053C | HXK1 | SGDID:S000001949 | HXK2 HEX1 HKB YGL253W NRB486 |
Hexokinase-2 (EC 2.7.1.1) (Hexokinase PII) (Hexokinase-B) |
2.7.1.1 | Saccharomyces cerevisiae | 2yhx_a | P04807 | 100.00 | 4.20E-43 | 2.80E-47 | 348.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YFR053C | HXK1 | SGDID:S000001949 | HXK6 HXK2 Os01g0742500 LOC_Os01g53930 P0439E07.19 |
Hexokinase-6 (EC 2.7.1.1) (Hexokinase-2) |
2.7.1.1 | Oryza sativa | 6jj4_a | Q8LQ68 | 100.00 | 1.10E-42 | 7.60E-47 | 346.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YFR053C | HXK1 | SGDID:S000001949 | HXK |
Hexokinase (EC 2.7.1.1) |
2.7.1.1 | Schistosoma mansoni | 1bdg_a | Q26609 | 100.00 | 1.90E-39 | 1.20E-43 | 321.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YFR053C | HXK1 | SGDID:S000001949 | GCK |
Hexokinase-4 (HK4) (EC 2.7.1.1) (Glucokinase) (Hexokinase type IV) (HK IV) (Hexokinase-D) |
2.7.1.1 | Homo sapiens | Glucose Metabolism Disease,Factitious Disorder,Hyperglycemia,Gestational Diabetes,Prediabetes Syndrome,Neonatal Diabetes,Diabetes Mellitus,Monogenic Diabetes,Hyperinsulinism,Hypoglycemia,Sudden Infant Death Syndrome,Type 1 Diabetes Mellitus,Hyperinsulinemic Hypoglycemia,Intestinal Atresia,Glucose Intolerance,Wolfram Syndrome,Maturity-Onset Diabetes Of The Young, Type 10,Hyperinsulinemic Hypoglycemia, Familial, 3,Clopidogrel Resistance,Maturity-Onset Diabetes Of The Young, Type 8, With Exocrine Dysfunction,Greig Cephalopolysyndactyly Syndrome,Hyperinsulinemic Hypoglycemia, Familial, 7,Fructose-1,6-Bisphosphatase Deficiency,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,3-Hydroxyacyl-Coa Dehydrogenase Deficiency,Maturity-Onset Diabetes Of The Young, Type 7,Maturity-Onset Diabetes Of The Young, Type 1,Maturity-Onset Diabetes Of The Young, Type 2,Type 2 Diabetes Mellitus,Insulinoma,Pancreatic Cystadenoma,Abdominal Obesity-Metabolic Syndrome 1,Diabetes Mellitus, Permanent Neonatal, 1,Maturity-Onset Diabetes Of The Young,Maturity-Onset Diabetes Of The Young, Type 4,Maturity-Onset Diabetes Of The Young, Type 6,Renal Cysts And Diabetes Syndrome,Maturity-Onset Diabetes Of The Young, Type 13,Maturity-Onset Diabetes Of The Young, Type 9,Hyperinsulinemic Hypoglycemia, Familial, 6,Donohue Syndrome,Pancreatic Agenesis,Maturity-Onset Diabetes Of The Young, Type 14,Munchausen By Proxy,Transient Neonatal Diabetes Mellitus,Permanent Neonatal Diabetes Mellitus,Maturity-Onset Diabetes Of The Young, Type 3 |
3f9m_a | P35557 | ENSG00000106633 | GCK | 100.00 | 8.60E-41 | 5.70E-45 | 332.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YFR053C | HXK1 | SGDID:S000001949 | HK1 |
Hexokinase-1 (EC 2.7.1.1) (Brain form hexokinase) (Hexokinase type I) (HK I) (Hexokinase-A) |
2.7.1.1 | Homo sapiens | Retinitis Pigmentosa,Diabetes Mellitus,Amyotrophic Lateral Sclerosis 1,Fundus Dystrophy,Retinitis Pigmentosa 79,Neuropathy,Charcot-Marie-Tooth Disease,Hemolytic Anemia,Hyperinsulinemic Hypoglycemia, Familial, 7,Cone-Rod Dystrophy 2,Hemolytic Anemia, Nonspherocytic, Due To Hexokinase Deficiency,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Neuropathy, Hereditary Motor And Sensory, Russe Type,Autosomal Recessive Disease,Neurodevelopmental Disorder With Visual Defects And Brain Anomalies,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome |
1cza_n | P19367 | ENSG00000156515 | HK1 | 100.00 | 2.80E-40 | 1.90E-44 | 355.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |