| Protein | Synonyms | Taxonomy |
|---|---|---|
| Sodium/glucose cotransporter 1 | Na(+)/glucose cotransporter 1; High affinity sodium-glucose cotransporter; Solute carrier family 5 member 1 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit beta-1 | Sodium/potassium-dependent ATPase subunit beta-1 | Homo sapiens (human) |
| Lactase-phlorizin hydrolase | Lactase-glycosylceramidase | Homo sapiens (human) |
| Solute carrier family 2, facilitated glucose transporter member 2 | Glucose transporter type 2, liver; GLUT-2 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit alpha-4 | Na(+)/K(+) ATPase alpha-4 subunit; EC 7.2.2.13; Sodium pump subunit alpha-4 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit alpha-1 | Na(+)/K(+) ATPase alpha-1 subunit; EC 7.2.2.13; Sodium pump subunit alpha-1 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit alpha-3 | Na(+)/K(+) ATPase alpha-3 subunit; EC 7.2.2.13; Na(+)/K(+) ATPase alpha(III) subunit; Sodium pump subunit alpha-3 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit beta-2 | Adhesion molecule in glia; AMOG; Sodium/potassium-dependent ATPase subunit beta-2 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit alpha-2 | Na(+)/K(+) ATPase alpha-2 subunit; EC 7.2.2.13; Sodium pump subunit alpha-2 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit beta-3 | Sodium/potassium-dependent ATPase subunit beta-3; ATPB-3 | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit gamma | Na(+)/K(+) ATPase subunit gamma; FXYD domain-containing ion transport regulator 2; Sodium pump gamma chain | Homo sapiens (human) |
| Sodium/potassium-transporting ATPase subunit beta | Homo sapiens (human) |
| Compound | Description |
|---|---|
| Orthophosphate | |
| galactose | An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. |
| Glucose | A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement. |
| Adenosine Triphosphate | An adenine nucleotide containing three phosphate groups esterified to the sugar moiety. In addition to its crucial roles in metabolism adenosine triphosphate is a neurotransmitter. |
| adenosine diphosphate | Adenosine 5'-(trihydrogen diphosphate). An adenine nucleotide containing two phosphate groups esterified to the sugar moiety at the 5'-position. |
| potassium | An element in the alkali group of metals with an atomic symbol K, atomic number 19, and atomic weight 39.10. It is the chief cation in the intracellular fluid of muscle and other cells. Potassium ion is a strong electrolyte that plays a significant role in the regulation of fluid volume and maintenance of the WATER-ELECTROLYTE BALANCE. |
| Sodium | A member of the alkali group of metals. It has the atomic symbol Na, atomic number 11, and atomic weight 23. |
| Water | A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) |