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Ketohexokinase

From Wikipedia, the free encyclopedia
KHK
Ketohexokinase homodimer, Human
Identifiers
AliasesKHK, ketohexokinase, FRUCTU, Hepatic fructokinase
External IDsOMIM: 614058; MGI: 1096353; GeneCards: KHK
Available structures
PDBOrtholog search: PDBe RCSB
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
2.7.1.3↗↗↗↗
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000221
NM_006488

NM_008439
NM_001310524
NM_001310525
NM_001349066

RefSeq (protein)

NP_000212
NP_006479

NP_001297453
NP_001297454
NP_032465
NP_001335995

Location (UCSC)Chr 2: 27.09 – 27.1 MbChr 5: 31.08 – 31.09 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Ketohexokinase
Identifiers
EC no.2.7.1.3
CAS no.9030-50-6
Databases
BRENDAenzyme data
ExPASyNiceZyme view
KEGGenzyme entry
MetaCycmetabolic pathway
Rheareactions
PDB structuresRCSB PDB PDBe PDBsum
Search
PMCarticles
PubMedarticles
NCBIproteins

Ketohexokinase (or hepatic fructokinase) is an enzyme that catalyzes the phosphorylation of fructose to produce fructose-1-phosphate.

ATP + Fru    ADP + F1P
ATP + D-fructose → ADP + D-fructose-1-phosphate[5]

Isoforms

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In humans, ketohexokinase is encoded by the KHK gene, which produces two isoforms, KHK-A and KHK-C, through alternative splicing.

  • KHK-C is primarily expressed in the liver, kidney, and intestine. It has a high affinity for fructose (low Km) and is responsible for the majority of fructose metabolism.
  • KHK-A is ubiquitously expressed in many tissues at low levels. It has a significantly lower affinity for fructose (high Km) compared to the C isoform.[6]

Role in fructose metabolism

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Ketohexokinase catalyzes the first step of fructolysis by phosphorylating fructose to form fructose 1-phosphate. The resulting fructose 1-phosphate is subsequently cleaved by aldolase B, producing intermediates that enter central carbohydrate metabolism.[7]

In humans, the KHK-C isoform is responsible for most fructose metabolism in the liver, kidney, and intestine. Unlike glucose metabolism, fructose metabolism through ketohexokinase bypasses phosphofructokinase, a major regulatory step in glycolysis, allowing fructose to enter downstream metabolic pathways through fructolysis.[8]

KHK is not allosterically inhibited by ATP or by its immediate product, fructose 1-phosphate.[9]

Essential fructosuria

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Loss-of-function mutations in KHK cause essential fructosuria, a generally benign inherited condition. After consuming fructose, affected people can have increased circulating fructose and excrete a portion of the fructose in urine.[9]

References

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  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000138030 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000029162 – Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ↑ Bais R, James HM, Rofe AM, Conyers RA (1985). "The purification and properties of human liver ketohexokinase. A role for ketohexokinase and fructose-bisphosphate aldolase in the metabolic production of oxalate from xylitol". Biochem. J. 230 (1): 53–60. doi:10.1042/bj2300053. PMC 1152585. PMID 2996495.
  6. ↑ Diggle CP, Shires M, Leitch D, Brooke D, Carr IM, Markham AF, Hayward BE, Asipu A, Bonthron DT (2009). "Ketohexokinase: Expression and Localization of the Principal Fructose-metabolizing Enzyme". Journal of Histochemistry & Cytochemistry. 57 (8): 763–774. doi:10.1369/jhc.2009.953190. PMC 2713076. PMID 19365088.
  7. ↑ Iizuka, Katsumi (2023). "Recent Progress on Fructose Metabolism—Chrebp, Fructolysis, and Polyol Pathway". Nutrients. 15 (7): 1778. doi:10.3390/nu15071778. PMC 10096667. PMID 37049617.
  8. ↑ Mirtschink, Peter; Jang, Cholsoon; Arany, Zoltan; Krek, Wilhelm (2018). "Fructose metabolism, cardiometabolic risk, and the epidemic of coronary artery disease". European Heart Journal. 39 (26): 2497–2505. doi:10.1093/eurheartj/ehx518. PMC 6037111. PMID 29020416.
  9. 1 2 Herman, Mark A.; Birnbaum, Morris J. (2021). "Molecular Aspects of Fructose Metabolism and Metabolic Disease". Cell Metabolism. 33 (12): 2329–2354. doi:10.1016/j.cmet.2021.09.010. PMC 8665132. PMID 34619074.
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