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AHCY wt Allele

Known as: Adenosylhomocysteinase wt Allele, SAHH, adoHcyase 
Human AHCY wild-type allele is located in the vicinity of 20q11.22 and is approximately 32 kb in length. This allele, which encodes… 
National Institutes of Health

Related topics

Related topics

6 relations
20q11.22Adenosylhomocysteinase, humanAmino Acid BiosynthesisHydrolysis

Broader (1)

AHCY gene

Papers overview

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2015
2015
Corrective effects of hepatotoxicity by hepatic Dyrk1a gene delivery in mice with intermediate hyperhomocysteinemia
2008
2008
Comparative kinetics of cofactor association and dissociation for the human and trypanosomal S-adenosylhomocysteine hydrolases. 2. The role of helix 18 stability.
The S-adenosyl- l-homocysteine (AdoHcy) hydrolases (SAHH) from Homo sapiens (Hs-SAHH) and from the parasite Trypanosoma cruzi (Tc… 
2007
2007
Comparative kinetics of cofactor association and dissociation for the human and trypanosomal S-adenosylhomocysteine hydrolases. 1. Basic features of the association and dissociation processes.
The S-adenosyl-l-homocysteine (AdoHcy) hydrolases catalyze the reversible conversion of AdoHcy to adenosine and homocysteine… 
2007
2007
Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3
S-adenosylhomocysteine hydrolase (AdoHcyase) catalyzes the hydrolysis of AdoHcy to adenosine and homocysteine. Increased levels… 
2006
2006
A single mutation at Tyr143 of human S-adenosylhomocysteine hydrolase renders the enzyme thermosensitive and affects the oxidation state of bound cofactor nicotinamide-adenine dinucleotide.
Recently, we have described the first human case of AdoHcyase (S-adenosylhomocysteine hydrolase) deficiency. Two point mutations… 
2004
2004
Homogeneous enzymatic colorimetric assay for total cysteine.
Patients with vascular disease have significantly higher concentrations of plasma total cysteine (tCYS) than do healthy… 
2003
2003
Capillary electrophoresis in diagnosis and monitoring of adenosine deaminase deficiency.
BACKGROUND The diagnosis and monitoring of severe combined immunodeficiency disease (SCID) attributable to adenosine deaminase… 
2001
2001
E1 mice epilepsy shows genetic polymorphism for s-Adenosyl-l-homocysteine hydrolase
1987
1987
Family and population studies of SAHH and ADA polymorphisms. A possible pitfall in the ascertainment of SAHH electrophoretic phenotypes
Typing of both SAHH and ADA red cell electrophoretic patterns was carried out among the members of about 80 families from Latium… 
1986
1986
Altered methylation complex isozymes as selective targets for cancer chemotherapy.
MC2 is a ternary enzyme complex consisting of MAT, methyltransferase and SAHH. Three isozymes of SAHH have been identified from… 
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