GGT1(1-380) R107H

Stable Identifier
R-HSA-5602863
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
GGT1 heavy chain, GGT1, GGT1hc, Gamma-glutamyltranspeptidase 1, GGT1_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
GGT1, GGT
Chain
chain:1-380, chain:381-569
Other Identifiers
0004120064
0006290338
00430+2.3.2.2
00460+2.3.2.2
00480+2.3.2.2+3.4.19.13
102724197
11741396_s_at
16928293
17122238
17122240
17122242
17123034
17123036
17123038
207131_3p_x_at
207131_x_at
208284_3p_x_at
208284_x_at
209919_3p_x_at
209919_x_at
211417_3p_x_at
211417_x_at
215603_x_at
2678
32893_s_at
41868_at
45635
47534
4GDX
4GG2
4Z9O
4ZBK
4ZC6
4ZCG
5V4Q
65444
715_s_at
728441
76993_f_at
8071927
8074316
A0A140VJJ9
A_21_P0012281
A_23_P154986
AAA02884
AAA02886
AAA35889
AAA35899
AAA52546
AAA52547
AAH25927
AAH69473
AAH69504
AAI28239
AAI28240
AEE60986
AP000356
BC025927
BC069473
BC069504
BC128238
BC128239
CAA42674
CAG30380
CCDS42992
CR456494
ENSG00000100031
ENSP00000248923
ENSP00000383231
ENSP00000383232
ENSP00000384381
ENSP00000384820
ENSP00000385445
ENSP00000387499
ENST00000248923
ENST00000400380
ENST00000400382
ENST00000401885
ENST00000403838
ENST00000404532
ENST00000425895
EntrezGene:102724197
EntrezGene:2678
EntrezGene:728441
g306748_3p_s_at
g306752_3p_s_at
g306752_3p_x_at
g306754_3p_s_at
g306754_3p_x_at
g9845490_3p_s_at
g9845492_3p_s_at
GE62999
GGT1
GGT1-201
GGT1-202
GGT1-203
GGT1-204
GGT1-205
GGT1-207
GGT1-213
GGT2
GO:0000003
GO:0002376
GO:0002682
GO:0002951
GO:0003674
GO:0005515
GO:0005575
GO:0005576
GO:0005615
GO:0005623
GO:0005886
GO:0006412
GO:0006508
GO:0006520
GO:0006536
GO:0006629
GO:0006691
GO:0006749
GO:0006750
GO:0006751
GO:0006790
GO:0006805
GO:0006950
GO:0007283
GO:0008150
GO:0008233
GO:0009056
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0016746
GO:0016787
GO:0019344
GO:0031638
GO:0034641
GO:0036374
GO:0043226
GO:0044281
GO:0050727
GO:0051604
GO:0070062
GO:0102953
GO:1901750
HGNC:4250
HM005386
HPA045635
HPA047534
HPA065444
Hs.314108.0.A1_3p_s_at
ILMN_1652604
ILMN_1663324
ILMN_1669393
ILMN_1686531
ILMN_1722975
ILMN_1787180
ILMN_1813658
ILMN_2274240
ILMN_2368585
IPR000101
IPR029055
J04131
J05235
L20490
L20493
LOC102724197
M24087
M24903
MIM:137181
MIM:231950
MIM:612346
NM_001288833
NM_013421
NM_013430
NP_001275762
NP_038265
NP_038347
PF01019
PH_hs_0028212
PH_hs_0032802
PH_hs_0033869
PH_hs_0040704
PR01210
PWY-4041
PWY-5826
TC22001026.hg
TC22001235.hg
TC22001460.hg
uc003aan.2
uc003aat.3
uc003aaw.3
uc003aay.1
uc062clh.1
uc062cll.1
uc062clm.1
UPI000007080C
UPI0000073F8C
UPI00001753A8
X60069
Participant Of
Other forms of this molecule
Modified Residues
Name
L-arginine 107 replaced with L-histidine
Coordinate
107
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-histidine.
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
inherited metabolic disorder 655 Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
Cross References
GeneCards
DOCK Blaster
ZINC target
PRO
HMDB Protein