Re***ed searches : Related searches
hexokinase gene,pyruvate kinase gene,phosphoglucose isomerase gene,pfk gene,hexokinase 1 vs 4,hexokinase function,glucokinase,hexokinase iv
Na***nal Institutes of Health (.gov) : 3098 - Gene ResultHK1 hexokinase 1 [ (human)]
Jun 21, 2023 — Hexokinase 1 (HK1) is a mitochondrial protein that controls the tramsmembrane potential and blocks apoptotic signals at the mitochondria. An ...
Pe***e also ask : What is the disease HK1?
HK1 (Hexokinase 1) is a Protein Coding gene. Diseases associated with HK1 include Hemolytic Anemia, Nonspherocytic, Due To Hexokinase Deficiency and Neuropathy, Hereditary Motor And Sensory, Russe Type. Among its related pathways are glycolysis (BioCyc) and trehalose degradation.
Pe***e also ask : What is the function of hexokinase 1?
Hexokinase 1 (HK1): Hexokinase 1 is another member of the mitochondrial hexokinase family, like glucokinase; it catalyzes the first step in glycolysis, namely, the conversion of glucose into glucose-6-phosphate.
Pe***e also ask : What is hexokinase type 1?
Hexokinase type I has a low Km and therefore a high affinity for glucose. This allows the initiation of glycolysis even when blood glucose levels are relatively low.
Pe***e also ask : Where is hexokinase 1 located?
In particular, HK1 is the most ubiquitously expressed isoform out of the four hexokinases, and constitutively expressed in most tissues, though it is majorly found in brain, kidney, and red blood cells (RBCs).
Ge***ards : HK1 Gene - HXK1 Protein
HK1 (Hexokinase 1) is a Protein Coding gene. Diseases associated with HK1 include Hemolytic Anemia, Nonspherocytic, Due To Hexokinase Deficiency and ...
Wi***edia : HK1
Hexokinase-1 (HK1) is an enzyme that in humans is encoded by the HK1 gene on chromosome 10. Hexokinases phosphorylate glucose to produce glucose-6-phosphate ...
Sc***ceDirect : HK1 - an overview
Hexokinase (HK), the red cell enzyme with the lowest activity in the glycolytic pathway, catalyzes the initial step in the utilization of glucose and thus is ...
Ca***for-Rare America : HK1 | Care-for-Rare America Inc.
The HK1 gene encodes the Hexokinase 1 enzyme, which is involved in glucose metabolism. A mutation of this enzyme leads to a decrease of energy in the brain.
On***e Mendelian Inheritance in Man : Entry - *142600 - HEXOKINASE 1; HK1
1.1) catalyzes the first step in glucose metabolism, using ATP for the phosphorylation of glucose to glucose-6-phosphate. Four different forms of hexokinase, ...
Na***e Journal : De novo variants in HK1 associated with ...
by V Okur · 2019 · Cited by 20 — Homozygous and heterozygous variants in HK1 have been shown to cause autosomal recessive non-spherocytic hemolytic anemia, autosomal recessive ...
Un***ot : HK1 - Hexokinase-1 - Homo sapiens (Human) | UniProtKB
An autosomal recessive progressive peripheral neuropathy characterized by onset in the first decade of distal lower limb weakness and muscle atrophy ...
IO***| ARVO Journals : A Dominant Mutation in Hexokinase 1 (HK1) Causes Retinitis ...
by LS Sullivan · 2014 · Cited by 52 — The HK1 gene encodes the hexokinase 1 protein, best known as the enzyme that catalyzes the first step of glycolysis. Inside the photoreceptor, glucose is ...