- of
fumarase:
Fumarase A,
Fumarase B, and
Fumarase C.
Fumarase A and
Fumarase B from
Escherichia coli are
classified as
class I,
whereas Fumarase C is...
-
Fumarase deficiency (or
fumaric aciduria) is an
exceedingly rare
autosomal recessive metabolic disorder in the
Krebs cycle,
characterized by a deficiency...
-
complement control protein Family history FH, a gene that
encodes the
enzyme fumarase Ferrihydrite (Fh), a
widespread hydrous ferric oxyhydroxide mineral McDonnell...
- of the
Short Cr****
Community are
reported to have a high
incidence of
fumarase deficiency, an
extremely rare
genetic disease. It
causes encephalopathy...
- trans-Enol-oxaloacetate also
appears when
tartrate is the
substrate for
fumarase.
Oxaloacetate forms in
several ways in nature. A prin****l
route is upon...
- {\displaystyle K_{\mathrm {m} }} .
Diffusion limited enzymes, such as
fumarase, work at the
theoretical upper limit of 108 – 1010 M−1s−1,
limited by diffusion...
- triose-phosphate isomerase,
carbonic anhydrase, acetylcholinesterase, catalase,
fumarase, β-lactamase, and
superoxide di****ase.: 8.4.2 The
turnover of such enzymes...
-
enzyme succinate dehydrogenase.
Fumarate is then
converted by the
enzyme fumarase to malate.
Human skin
naturally produces fumaric acid when
exposed to sunlight...
- The
fumarate released in the
cytosol is
hydrated to
malate by
cytosolic fumarase. This
malate is then
oxidized to
oxaloacetate by
cytosolic malate dehydrogenase...
- dehydrogenase, α-ketoglutarate dehydrogenase, succinyl-CoA synthetase,
fumarase, and
malate dehydrogenase. The urea
cycle is
facilitated by
carbamoyl phosphate...
