Guanidinoacetate N-methyltransferase: Difference between revisions

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*{{cite journal  | author=Grimwood J |title=The DNA sequence and biology of human chromosome 19 |journal=Nature |volume=428 |issue= 6982 |pages= 529–35 |year= 2004 |pmid= 15057824 |doi= 10.1038/nature02399  |name-list-format=vanc| author2=Gordon LA  | author3=Olsen A  | display-authors=3  | last4=Terry  | first4=Astrid  | last5=Schmutz  | first5=Jeremy  | last6=Lamerdin  | first6=Jane  | last7=Hellsten  | first7=Uffe  | last8=Goodstein  | first8=David  | last9=Couronne  | first9=Olivier }}
*{{cite journal  | author=Grimwood J |title=The DNA sequence and biology of human chromosome 19 |journal=Nature |volume=428 |issue= 6982 |pages= 529–35 |year= 2004 |pmid= 15057824 |doi= 10.1038/nature02399  |name-list-format=vanc| author2=Gordon LA  | author3=Olsen A  | display-authors=3  | last4=Terry  | first4=Astrid  | last5=Schmutz  | first5=Jeremy  | last6=Lamerdin  | first6=Jane  | last7=Hellsten  | first7=Uffe  | last8=Goodstein  | first8=David  | last9=Couronne  | first9=Olivier }}
*{{cite journal  | author=Strausberg RL |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241  |name-list-format=vanc| author2=Feingold EA  | author3=Grouse LH  | display-authors=3  | last4=Derge  | first4=JG  | last5=Klausner  | first5=RD  | last6=Collins  | first6=FS  | last7=Wagner  | first7=L  | last8=Shenmen  | first8=CM  | last9=Schuler  | first9=GD }}
*{{cite journal  | author=Strausberg RL |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241  |name-list-format=vanc| author2=Feingold EA  | author3=Grouse LH  | display-authors=3  | last4=Derge  | first4=JG  | last5=Klausner  | first5=RD  | last6=Collins  | first6=FS  | last7=Wagner  | first7=L  | last8=Shenmen  | first8=CM  | last9=Schuler  | first9=GD }}
*{{cite journal  | author=Komoto J |title=Crystallization and preliminary x-ray diffraction studies of guanidinoacetate methyltransferase from rat liver |journal=Acta Crystallogr. D |volume=55 |issue= Pt 11 |pages= 1928–9 |year= 2000 |pmid= 10531498 |doi=10.1107/S0907444999010318  |name-list-format=vanc| author2=Huang Y  | author3=Hu Y  | display-authors=3  | last4=Takata  | first4=Yoshimi  | last5=Konishi  | first5=Kiyoshi  | last6=Ogawa  | first6=Hirofumi  | last7=Gomi  | first7=Tomoharu  | last8=Fujioka  | first8=Motoji  | last9=Takusagawa  | first9=Fusao  }}
*{{cite journal  | author=Komoto J |title=Crystallization and preliminary x-ray diffraction studies of guanidinoacetate methyltransferase from rat liver |journal=Acta Crystallogr. D |volume=55 |issue= Pt 11 |pages= 1928–9 |year= 2000 |pmid= 10531498 |doi=10.1107/S0907444999010318  |name-list-format=vanc| author2=Huang Y  | author3=Hu Y  | display-authors=3  | last4=Takata  | first4=Yoshimi  | last5=Konishi  | first5=Kiyoshi  | last6=Ogawa  | first6=Hirofumi  | last7=Gomi  | first7=Tomoharu  | last8=Fujioka  | first8=Motoji  | last9=Takusagawa  | first9=Fusao  |url=https://kuscholarworks.ku.edu/bitstream/1808/17175/1/TakusagawaF_AC_55%2811%291928.pdf}}
*{{cite journal  | author=Chae YJ |title=The gene encoding guanidinoacetate methyltransferase (GAMT) maps to human chromosome 19 at band p13.3 and to mouse chromosome 10 |journal=Genomics |volume=49 |issue= 1 |pages= 162–4 |year= 1998 |pmid= 9570966 |doi= 10.1006/geno.1998.5236  |name-list-format=vanc| author2=Chung CE  | author3=Kim BJ  | display-authors=3  | last4=Lee  | first4=MH  | last5=Lee  | first5=H }}
*{{cite journal  | author=Chae YJ |title=The gene encoding guanidinoacetate methyltransferase (GAMT) maps to human chromosome 19 at band p13.3 and to mouse chromosome 10 |journal=Genomics |volume=49 |issue= 1 |pages= 162–4 |year= 1998 |pmid= 9570966 |doi= 10.1006/geno.1998.5236  |name-list-format=vanc| author2=Chung CE  | author3=Kim BJ  | display-authors=3  | last4=Lee  | first4=MH  | last5=Lee  | first5=H }}
*{{cite journal  |vauthors=Jenne DE, Olsen AS, Zimmer M |title=The human guanidinoacetate methyltransferase (GAMT) gene maps to a syntenic region on 19p13.3, homologous to band C of mouse chromosome 10, but GAMT is not mutated in jittery mice |journal=Biochem. Biophys. Res. Commun. |volume=238 |issue= 3 |pages= 723–7 |year= 1997 |pmid= 9325156 |doi= 10.1006/bbrc.1997.9992 }}
*{{cite journal  |vauthors=Jenne DE, Olsen AS, Zimmer M |title=The human guanidinoacetate methyltransferase (GAMT) gene maps to a syntenic region on 19p13.3, homologous to band C of mouse chromosome 10, but GAMT is not mutated in jittery mice |journal=Biochem. Biophys. Res. Commun. |volume=238 |issue= 3 |pages= 723–7 |year= 1997 |pmid= 9325156 |doi= 10.1006/bbrc.1997.9992 }}

Latest revision as of 14:09, 4 November 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human
guanidinoacetate N-methyltransferase
Identifiers
EC number2.1.1.2
CAS number9029-75-8
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO

Guanidinoacetate N-methyltransferase (EC 2.1.1.2) is an enzyme that catalyzes the chemical reaction and is encoded by gene GAMT located on chromosome 19p13.3.[1]

S-adenosyl-L-methionine + guanidinoacetate <math>\rightleftharpoons</math> S-adenosyl-L-homocysteine + creatine

Thus, the two substrates of this enzyme are S-adenosyl methionine and guanidinoacetate, whereas its two products are S-adenosylhomocysteine and creatine.

This enzyme belongs to the family of transferases, specifically those transferring one-carbon group methyltransferases. The systematic name of this enzyme class is S-adenosyl-L-methionine:N-guanidinoacetate methyltransferase. Other names in common use include GA methylpherase, guanidinoacetate methyltransferase, guanidinoacetate transmethylase, methionine-guanidinoacetic transmethylase, and guanidoacetate methyltransferase. This enzyme participates in glycine, serine and threonine metabolism and arginine and proline metabolism.

The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals. Two transcript variants encoding different isoforms have been described for this gene.[1]

Structural studies

As of late 2007, 7 structures have been solved for this class of enzymes, with PDB accession codes 1KHH, 1P1B, 1P1C, 1XCJ, 1XCL, 1ZX0, and 2BLN.

See also

References

  1. 1.0 1.1 "Entrez Gene: GAMT guanidinoacetate N-methyltransferase".