Glycerate kinase

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== Disease ==
== Disease ==
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Mutation in GK is the cause of inherited D-glyceric acidemia) (D-glyceric aciduria)<ref>PMID:20949620</ref>.
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Mutation in GK is the cause of inherited D-glyceric acidemia (D-glyceric aciduria)<ref>PMID:20949620</ref>.
</StructureSection>
</StructureSection>
== 3D Structures of glycerate kinase ==
== 3D Structures of glycerate kinase ==

Current revision

Glycerate kinase dimer complex with sulfate ions (PDB code 1to6).

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3D Structures of glycerate kinase

Updated on 03-March-2020

1to6 – GK – Neisseria meningitides
2b8n – GK – Thermotoga maritima
1x3l – GK – Pyrococcus horikoshii
3cwc – GK – Salmonella enterica
6ckg – GK – Cryptococcus neoformans

References

  1. ↑ Doughty CC, Hayashi JA, Guenther HL. Purification and properties of D-glycerate 3-kinase from Escherichia coli. J Biol Chem. 1966 Feb 10;241(3):568-72. PMID:5325263
  2. ↑ Sass JO, Fischer K, Wang R, Christensen E, Scholl-Burgi S, Chang R, Kapelari K, Walter M. D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK). Hum Mutat. 2010 Dec;31(12):1280-5. doi: 10.1002/humu.21375. Epub 2010 Nov 9. PMID:20949620 doi:http://dx.doi.org/10.1002/humu.21375

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky, Joel L. Sussman, Eran Hodis

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