KEGG   ORTHOLOGY: K14592Help
Entry
K14592                      KO                                     

Name
FOLH1, GCPII
Definition
glutamate carboxypeptidase II (folate hydrolase 1) [EC:3.4.17.21]
Pathway
Alanine, aspartate and glutamate metabolism
Vitamin digestion and absorption
Brite
KEGG Orthology (KO) [BR:ko00001]
 Metabolism
  Amino acid metabolism
   00250 Alanine, aspartate and glutamate metabolism
    K14592  FOLH1, GCPII; glutamate carboxypeptidase II (folate hydrolase 1)
 Organismal Systems
  Digestive system
   04977 Vitamin digestion and absorption
    K14592  FOLH1, GCPII; glutamate carboxypeptidase II (folate hydrolase 1)
Enzymes [BR:ko01000]
 3. Hydrolases
  3.4  Acting on peptide bonds (peptidases)
   3.4.17  Metallocarboxypeptidases
    3.4.17.21  glutamate carboxypeptidase II
     K14592  FOLH1, GCPII; glutamate carboxypeptidase II (folate hydrolase 1)
Peptidases [BR:ko01002]
 Metallo Peptidases
  Family M28: aminopeptidase Y family
   K14592  FOLH1, GCPII; glutamate carboxypeptidase II (folate hydrolase 1)
BRITE hierarchy
Other DBs
Genes
HSA: 
2346(FOLH1)
PTR: 
451185(FOLH1) 451475
PPS: 
GGO: 
101147888(FOLH1)
PON: 
100453848(FOLH1)
MCC: 
707714(FOLH1)
MCF: 
MMU: 
53320(Folh1)
RNO: 
85309(Folh1)
CGE: 
HGL: 
101725016(Folh1)
TUP: 
102487205(FOLH1B)
CFA: 
476775(FOLH1)
AML: 
FCA: 
101089641(FOLH1B)
PTG: 
102957765(FOLH1B)
BTA: 
505865(FOLH1)
BOM: 
102272952(FOLH1B)
PHD: 
102323016(FOLH1B)
CHX: 
102190665(FOLH1B)
SSC: 
397677(FOLH1)
CFR: 
102510657(FOLH1B)
BACU: 
LVE: 
ECB: 
100060132(FOLH1B)
MYB: 
MYD: 
102761189(FOLH1B)
PALE: 
102895068(FOLH1B)
MDO: 
SHR: 
OAA: 
GGA: 
419011(FOLH1)
MGP: 
TGU: 
FAB: 
101814982(FOLH1)
PHI: 
102105283(FOLH1B)
APLA: 
FPG: 
FCH: 
102058819(FOLH1B)
CLV: 
102095234(FOLH1B)
ASN: 
102387587(FOLH1B)
AMJ: 
PSS: 
102455710(FOLH1B)
CMY: 
102934118(FOLH1B)
ACS: 
PBI: 
XTR: 
100485577(folh1)
BFO: 
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Guo J, Xie H, Wang J, Zhao H, Wang F, Liu C, Wang L, Lu X, Bao Y, Zou J, Wang G, Niu B, Zhang T
  Title
The maternal folate hydrolase gene polymorphism is associated with neural tube defects in a high-risk Chinese population.
  Journal
Genes Nutr 8:191-7 (2013)

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