Protein Shmt1

URN urn:agi-llid:6470
Connectivity 42
Name Shmt1
Description serine hydroxymethyltransferase 1 (soluble)
Notes This gene encodes the cellular form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing of this gene results in 2 transcript variants encoding 2 different isoforms. Additional transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq]

Pathway folate cycle metabolic pathway
folated mediated one carbon metabolic pathway

GO Molecular Function catalytic activity
transferase activity
amino acid binding
pyridoxal phosphate binding
protein homodimerization activity
methyltransferase activity
glycine hydroxymethyltransferase activity
L-allo-threonine aldolase activity

GO Cellular Component cytoplasm
cytosol
mitochondrion

GO Biological Process one-carbon metabolic process
folic acid metabolic process
purine base biosynthetic process
glycine biosynthetic process
glycine biosynthetic process from serine
L-serine catabolic process
glycine metabolic process
L-serine metabolic process
protein tetramerization
protein homotetramerization

Ariadne Ontology Ser-Gly metabolism

Group Ser-Gly metabolism
catalytic activity
one-carbon metabolic process
folic acid metabolic process
purine base biosynthetic process
glycine biosynthetic process
glycine biosynthetic process from serine
L-serine catabolic process
glycine metabolic process
L-serine metabolic process
protein tetramerization
protein homotetramerization
transferase activity
amino acid binding
pyridoxal phosphate binding
protein homodimerization activity
methyltransferase activity
glycine hydroxymethyltransferase activity
L-allo-threonine aldolase activity
cytoplasm
cytosol
mitochondrion

MedScan ID 6470

Hugo ID 10850

Human chromosome position 17p11.2

LocusLink ID 6470
20425
287379

Alias SHMT
CSHMT
MGC15229
MGC24556
serine hydroxymethyltransferase, cytosolic
14 kDa protein
serine methylase
glycine hydroxymethyltransferase
cytoplasmic serine hydroxymethyltransferase
mshmt
C81125
mshmt1
mshmt2
AI324848
AI385541
RP23-278I21.7
OTTMUSP00000008170
LRRGT00032
cytosolic Serine hydroxymethyltransferase
Glycine hydroxymethyltransferase 1
Glycine hydroxymethyltransferase I
mshmt I
serine hydroxymethyl transferase 1
serine hydroxymethyl transferase 1 (soluble)
serine hydroxymethyl transferase I
serine hydroxymethyltransferase 1
serine hydroxymethyltransferase 1 (soluble)
serine hydroxymethyltransferase I
Serine methylase 1
Serine methylase I
SHMT I
SHMT1
soluble serine hydroxymethyltransferase

Organism Homo sapiens
Mus musculus
Rattus norvegicus

GenBank ID NC_000017
NM_148918
NP_683718
NM_004169
NP_004160
NT_010718
NW_926628
NW_001838410
AC_000060
AC_000149
AC127537
AF017064
AL353997
CH471196
EAW55637
EAW55638
EAW55639
EAW55640
EAW55641
EAW55642
EAW55643
Y14489
CAB54842
Y14490
CAB54843
AF017065
AAC39726
AK223552
BAD97272
AK298415
BAG60641
AK302834
BAG64027
BC007979
AAH07979
BC022874
AAH22874
BC038598
AAH38598
CR592100
CR594273
CR599388
CR613144
L11931
AAA63257
L23928
AAA36018
AAA36019
AAA36020
Y14485
CAB54838
Y14486
CAB54839
Y14488
CAB54841
P34896
Q53ET7
Q9UMC8
Q9UMC9
Q9UMD0
DQ893242
ABM84168
EU176779
ABW03580
NC_000077
NM_009171
NP_033197
NT_096135
AL596215
CAI35264
CH467490
EDL01257
AF237702
AAK15040
AK010439
BAB26940
AK132342
BC026055
AAH26055
BQ832130
BQ942592
CF159149
X94478
CAA64225
X94479
CAA64226
P50431
Q8R0X9
Q9CWR5
NC_005109
NM_001047842
NW_047334
NW_001084656
AC_000078
AY383687
AAQ96245
BC099219
AAH99219
Q4KLG7
Q6TXG7

OMIM ID 182144

Mouse chromosome position 11

GO ID 0008732
0016597
0004372
0042803
0030170
0016740
0006565
0046655
0019264
0006730
0051289
0051262
0009113
0005737
0005829
0005739
0003824
0008168
0006563
0006545
0006544

Rat chromosome position 10q22

Swiss-Prot Accession P34896
Q53ET7
Q9UMC8
Q9UMC9
Q9UMD0
Q8R0X9
P50431
Q9CWR5
Q6TXG7
Q4KLG7
Q96HY0
Q9UMD1
Q9UMD2

PIR ID A46746

Unigene ID Hs.513987
Hs.636044
Mm.364956
Rn.3684

KEGG ID hsa:6470
mmu:20425
rno:287379

EC Number 2.1.2.1

Swiss-Prot ID GLYC_HUMAN
Q6TXG7_RAT
Q8R0X9_MOUSE
Q96HY0_HUMAN

Cell Localization Cytoplasm

IPI ID IPI00002519
IPI00220668
IPI00220669
IPI00421364
IPI00608017
IPI00008665
IPI00793862
IPI00791841
IPI00796912
IPI00118059
IPI00627076

Homologene ID 3074

RGD ID 1312011

MGI ID 98299