Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

18 structures for P78417

Entry ID Method Resolution Chain Position Source
1EEM X-ray 200 A A 1-241 PDB
3LFL X-ray 210 A A/B/C 1-241 PDB
3VLN X-ray 170 A A 1-241 PDB
4IS0 X-ray 172 A A 1-241 PDB
4YQM X-ray 238 A A/B/C 1-241 PDB
4YQU X-ray 194 A A/B 1-241 PDB
4YQV X-ray 206 A A/B/C 1-241 PDB
5UEH X-ray 200 A A 1-241 PDB
5V3Q X-ray 225 A A 1-241 PDB
5YVN X-ray 133 A A 1-241 PDB
5YVO X-ray 180 A A 1-241 PDB
6MHB X-ray 275 A A/B/C/D/E/F 1-241 PDB
6MHC X-ray 200 A A/B 1-241 PDB
6MHD X-ray 216 A A/B 1-241 PDB
6PNM X-ray 182 A A 2-241 PDB
6PNN X-ray 210 A A 2-241 PDB
6PNO X-ray 182 A A 2-241 PDB
AF-P78417-F1 Predicted AlphaFoldDB

202 variants for P78417

Variant ID(s) Position Change Description Diseaes Association Provenance
rs1003018292
CA212447651
2 S>C No ClinGen
TOPMed
CA5681430
rs772396594
CA5681429
3 G>R No ClinGen
ExAC
gnomAD
TCGA novel 4 E>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA378076528
rs1474909556
6 A>V No ClinGen
gnomAD
RCV000969856
rs72559704
CA5681432
7 R>K No ClinGen
ClinVar
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA378076533
rs72559704
7 R>M No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1251385813
CA378076540
8 S>T No ClinGen
TOPMed
rs776806870
CA378076544
9 L>V No ClinGen
ExAC
TOPMed
gnomAD
rs760104472
CA5681434
10 G>E No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 10 G>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs915721379
CA212447674
11 K>R No ClinGen
gnomAD
CA378076578
rs1258278989
12 G>E No ClinGen
TOPMed
gnomAD
rs752612056
CA5681464
13 S>R No ClinGen
ExAC
gnomAD
rs777727184
CA5681466
15 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA378076599
rs1376725101
15 P>S No ClinGen
gnomAD
CA5681468
rs771344081
16 P>L No ClinGen
ExAC
gnomAD
rs1564835315 16 P>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
rs370320075
CA212447958
16 P>T No ClinGen
ESP
TOPMed
TCGA novel 17 G>E Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1288941028
CA378076651
18 P>S No ClinGen
gnomAD
CA5681470
rs746005024
19 V>I No ClinGen
ExAC
gnomAD
CA378076681
rs1181667116
20 P>A No ClinGen
gnomAD
rs769727460
CA5681471
20 P>L No ClinGen
ExAC
TOPMed
gnomAD
rs769727460
CA5681472
20 P>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA5681473
rs149222313
22 G>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA378076772
rs1470661480
25 R>H No ClinGen
gnomAD
CA5681475
rs564705573
26 I>V No ClinGen
1000Genomes
ExAC
gnomAD
CA378076849
rs1364917793
29 M>I No ClinGen
gnomAD
CA5681477
rs146896093
29 M>T No ClinGen
ESP
ExAC
gnomAD
rs762154396
CA5681476
29 M>V No ClinGen
ExAC
rs45529437
CA5681479
32 C>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs45529437
CA5681478
VAR_061231
32 C>Y No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA5681481
rs752197685
33 P>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA5681480
rs764679950
33 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs1336993429
CA378076916
34 F>C No ClinGen
gnomAD
rs1448603478
CA378076947
36 E>K No ClinGen
TOPMed
CA378076971
rs1388272778
37 R>K No ClinGen
TOPMed
CA5681483
rs764125468
38 T>M No ClinGen
ExAC
gnomAD
CA5681484
rs751456497
39 R>C No ClinGen
ExAC
gnomAD
rs751456497
CA378076995
39 R>G No ClinGen
ExAC
gnomAD
rs978522988
CA212448014
39 R>L No ClinGen
gnomAD
CA5681486
rs781512367
41 V>A No ClinGen
ExAC
TOPMed
gnomAD
CA212448023
rs924378265
41 V>I No ClinGen
Ensembl
rs1564835405
CA378077056
44 A>V No ClinGen
Ensembl
rs780009826
CA5681489
45 K>E No ClinGen
ExAC
TOPMed
gnomAD
rs1415972337
CA378077070
45 K>N No ClinGen
TOPMed
gnomAD
rs780009826
CA378077059
45 K>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1186845498
CA378077068
45 K>R No ClinGen
gnomAD
rs1295829625
CA378077098
48 R>K No ClinGen
TOPMed
CA5681516
rs747397917
49 H>Q No ClinGen
ExAC
CA378078074
rs1380325561
49 H>R No ClinGen
gnomAD
CA378078095
rs1297390928
52 I>T No ClinGen
gnomAD
rs769393338
CA5681517
53 N>I No ClinGen
ExAC
TOPMed
gnomAD
rs769393338
CA378078102
53 N>S No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 54 I>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA212450216
rs1042620356
55 N>S No ClinGen
Ensembl
rs1019133448
CA212450219
57 K>E No ClinGen
TOPMed
rs968020753
CA378078174
61 E>K No ClinGen
TOPMed
gnomAD
CA212450225
rs968020753
61 E>Q No ClinGen
TOPMed
gnomAD
rs1296328958
CA378078189
62 W>G No ClinGen
TOPMed
CA212450232
rs775258075
63 F>L No ClinGen
ExAC
TOPMed
CA378078213
rs762588581
64 F>L No ClinGen
ExAC
gnomAD
rs762588581
CA5681519
64 F>V No ClinGen
ExAC
gnomAD
CA378078225
rs1589844717
65 K>E No ClinGen
Ensembl
rs763724479
CA5681520
67 N>S No ClinGen
ExAC
gnomAD
rs867668983
CA212450239
68 P>L No ClinGen
Ensembl
rs1188685675
CA378078264
68 P>S No ClinGen
gnomAD
CA378078271
rs1589844728
69 F>L No ClinGen
Ensembl
CA212450243
rs1008689901
70 G>A No ClinGen
Ensembl
rs374294843
CA5681523
73 P>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 74 V>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1337492547
CA378078343
76 E>G Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA378078410
rs1431116964
82 L>V No ClinGen
TOPMed
rs760498687
CA5681525
83 I>M No ClinGen
ExAC
gnomAD
CA378078420
rs1173648582
83 I>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs750251204
CA5681524
83 I>V No ClinGen
ExAC
TOPMed
gnomAD
rs747444602
CA378078437
CA378078435
84 Y>* No ClinGen
ExAC
TOPMed
gnomAD
COSM914534
CA5681527
rs754091728
85 E>K Variant assessed as Somatic; impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
rs11509436
CA212450257
VAR_029269
86 S>C No ClinGen
UniProt
TOPMed
dbSNP
gnomAD
rs1385375315
CA378078468
87 A>V No ClinGen
gnomAD
CA212450261
rs1018697878
89 T>I No ClinGen
Ensembl
CA378078498
rs1589844800
90 C>S No ClinGen
Ensembl
CA378078547
rs1215096671
94 D>A No ClinGen
TOPMed
CA378078583
rs1373009716
97 Y>* No ClinGen
gnomAD
rs1301153852
CA378078575
97 Y>H No ClinGen
TOPMed
gnomAD
CA378078573
rs1301153852
97 Y>N No ClinGen
TOPMed
gnomAD
rs752711264
CA5681530
98 P>L No ClinGen
ExAC
gnomAD
rs146967406
CA5681529
98 P>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA5681532
rs758896615
99 G>E No ClinGen
ExAC
gnomAD
rs1261738193
CA378078608
100 K>R No ClinGen
gnomAD
rs1212133493
CA378078626
101 K>N No ClinGen
gnomAD
CA378078622
rs1310487761
101 K>R No ClinGen
TOPMed
rs148006054
CA5681533
103 L>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs141645977
CA5681535
104 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 104 P>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA5681534
rs747379810
104 P>S No ClinGen
ExAC
gnomAD
rs748966808
CA5681537
106 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs748966808
CA378078668
106 D>Y No ClinGen
ExAC
TOPMed
gnomAD
rs150506133
CA5681540
107 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5681539
rs150506133
107 P>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs569087890
CA5681541
108 Y>C No ClinGen
1000Genomes
ExAC
gnomAD
CA5681542
rs773171640
109 E>K No ClinGen
ExAC
gnomAD
rs760491652
CA5681543
110 K>E No ClinGen
ExAC
gnomAD
CA212450322
rs916334054
111 A>G No ClinGen
TOPMed
gnomAD
rs1564836628
CA378078784
116 I>S No ClinGen
Ensembl
CA378078782
rs1564836628
116 I>T No ClinGen
Ensembl
CA378078801
rs1371252485
118 E>Q No ClinGen
gnomAD
TCGA novel 119 L>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA378078851
rs1307980105
122 K>T No ClinGen
gnomAD
CA378079330
rs1473004441
123 V>M No ClinGen
gnomAD
CA5681568
rs763042697
125 S>T No ClinGen
ExAC
TOPMed
gnomAD
rs557588649
CA5681569
125 S>Y No ClinGen
1000Genomes
ExAC
gnomAD
CA378079372
rs751531910
127 V>I No ClinGen
ExAC
TOPMed
gnomAD
CA5681571
rs751531910
127 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs1374901912
CA378079398
129 S>N No ClinGen
gnomAD
rs1031409217
CA212451533
129 S>R No ClinGen
TOPMed
gnomAD
CA5681572
rs575960084
131 I>N No ClinGen
1000Genomes
ExAC
gnomAD
rs139445649
CA5681574
133 S>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs756524212
CA5681575
133 S>R No ClinGen
ExAC
gnomAD
CA378079546
rs1346508228
137 E>D No ClinGen
TOPMed
gnomAD
rs780242946
CA5681577
137 E>Q No ClinGen
ExAC
TOPMed
gnomAD
rs955721136
CA212451545
139 Y>C No ClinGen
Ensembl
VAR_016811
rs4925
CA5681578
140 A>D allele GSTO1*C; no effect on protein stability [UniProt] No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs757930662
CA5681580
143 K>E No ClinGen
ExAC
rs771562518 145 E>missing Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
rs777343283
CA5681581
145 E>Q No ClinGen
ExAC
gnomAD
CA5681582
rs746500935
146 F>L No ClinGen
ExAC
gnomAD
rs777056461
CA5681584
147 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs141387929
CA5681585
147 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs141387929
CA5681586
147 R>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs777056461
CA5681583
147 R>S No ClinGen
ExAC
TOPMed
gnomAD
CA378079710
rs775096136
148 K>* No ClinGen
ExAC
gnomAD
CA5681587
rs775096136
148 K>E No ClinGen
ExAC
gnomAD
rs1394624522
CA378079732
149 E>* Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA212451573
rs1005666879
149 E>A No ClinGen
TOPMed
CA378079789
rs1175535889
150 F>C No ClinGen
gnomAD
CA212451576
rs954444943
150 F>L No ClinGen
TOPMed
gnomAD
CA378079865
rs1318102193
153 L>R No ClinGen
TOPMed
rs869031575
CA918751490
155 E>R No ClinGen
Ensembl
VAR_016813 155 E>del allele GSTO1*B; decreased protein stability [UniProt] No UniProt
CA378080896
rs1171295245
158 T>S No ClinGen
TOPMed
rs775355821
COSM1178275
CA5681607
159 N>D prostate [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
CA378080905
rs1237962921
159 N>S No ClinGen
gnomAD
rs200745440
CA5681608
161 K>T No ClinGen
1000Genomes
ExAC
gnomAD
rs369551343
CA5681609
162 T>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
RCV000888345
rs116993524
CA5681610
163 T>I No ClinGen
ClinVar
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA378080946
rs116993524
163 T>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 165 F>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA378080994
rs1260244599
167 G>D No ClinGen
TOPMed
rs761270521
CA5681614
168 N>K No ClinGen
ExAC
gnomAD
rs148403642
CA5681613
168 N>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA212452887
rs376039597
170 I>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA378081026
rs1165520884
170 I>T No ClinGen
Ensembl
rs376039597
COSM1627302
CA5681615
170 I>V liver [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs754290509
CA5681616
171 S>Y No ClinGen
ExAC
gnomAD
rs1279898487
CA378081063
172 M>I No ClinGen
TOPMed
rs369692828
CA5681617
173 I>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5681619
rs751246906
175 Y>C No ClinGen
ExAC
gnomAD
CA5681621
rs780689474
176 L>F No ClinGen
ExAC
gnomAD
CA378081145
rs780689474
176 L>V No ClinGen
ExAC
gnomAD
CA5681622
rs749866804
178 W>* No ClinGen
ExAC
gnomAD
rs201522765
CA5681623
179 P>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1292504288
CA378081284
183 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs779840419
CA5681624
183 R>W No ClinGen
ExAC
TOPMed
gnomAD
rs1235136197
CA378081334
186 A>T No ClinGen
gnomAD
rs1427312417
CA378081661
191 E>D No ClinGen
gnomAD
CA5681647
rs772481441
193 V>A No ClinGen
ExAC
gnomAD
rs1172415741
CA378081721
195 H>N No ClinGen
gnomAD
rs560168668
CA5681649
197 P>L No ClinGen
1000Genomes
ExAC
gnomAD
rs747154809
CA5681650
198 K>Q No ClinGen
ExAC
gnomAD
rs1274976017
CA378081868
202 W>G No ClinGen
TOPMed
CA378081895
rs1233433012
203 M>I No ClinGen
TOPMed
CA5681651
rs770951049
205 A>P No ClinGen
ExAC
gnomAD
CA212453414
rs532141559
206 M>I No ClinGen
1000Genomes
CA378081933
rs1383952851
206 M>V No ClinGen
gnomAD
VAR_024484
rs11509438
CA5681652
208 E>K No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA212453423
CA212453420
rs369926436
209 D>E No ClinGen
TOPMed
rs746372013
CA5681653
210 P>S No ClinGen
ExAC
CA5681655
rs770264722
211 T>P No ClinGen
ExAC
gnomAD
rs1233688548
CA378082097
214 A>P No ClinGen
TOPMed
gnomAD
CA378082095
rs1233688548
214 A>T No ClinGen
TOPMed
gnomAD
CA5681657
rs763287842
215 L>P No ClinGen
ExAC
gnomAD
CA378082153
rs15032
217 T>I No ClinGen
gnomAD
CA212453444
rs15032
217 T>N No ClinGen
gnomAD
CA5681660
rs772817786
220 K>R No ClinGen
ExAC
gnomAD
rs764766650
CA212453460
221 D>N No ClinGen
Ensembl
rs921626074
CA212453466
223 Q>E No ClinGen
Ensembl
rs1263505296
CA378082310
225 F>I No ClinGen
gnomAD
CA5681663
rs753323694
227 E>Q No ClinGen
ExAC
gnomAD
rs754940007
CA5681664
228 L>F No ClinGen
ExAC
gnomAD
rs569003679
CA5681665
229 Y>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs373305518
CA5681666
CA378082423
231 Q>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1176324895
CA378082419
231 Q>P No ClinGen
TOPMed
gnomAD
rs888045519
CA212453490
234 P>S No ClinGen
Ensembl
rs11509439
VAR_026583
CA5681668
236 A>V No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA212453505
rs986118514
237 C>Y No ClinGen
TOPMed
gnomAD
rs747220782
CA5681669
238 D>V No ClinGen
ExAC
gnomAD
CA378082477
rs1324025414
239 Y>* No ClinGen
gnomAD
rs148530043
CA5681670
239 Y>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA5681671
rs781132094
241 L>F No ClinGen
ExAC
gnomAD
rs1220103732
CA378082492
242 L>G No ClinGen
gnomAD
rs548093642
CA5681672
242 L>S No ClinGen
1000Genomes
ExAC
gnomAD

No associated diseases with P78417

3 regional properties for P78417

Type Name Position InterPro Accession
domain Glutathione S-transferase, N-terminal 22 - 101 IPR004045
domain Glutathione S-transferase, C-terminal 140 - 218 IPR004046
domain Glutathione S-transferase, C-terminal-like 106 - 230 IPR010987

Functions

Description
EC Number 1.8.5.1 With a quinone or similar compound as acceptor
Subcellular Localization
  • Cytoplasm, cytosol
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

3 GO annotations of cellular component

Name Definition
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
extracellular exosome A vesicle that is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane. Extracellular exosomes, also simply called exosomes, have a diameter of about 40-100 nm.

4 GO annotations of molecular function

Name Definition
glutathione dehydrogenase (ascorbate) activity Catalysis of the reaction: dehydroascorbate + 2 glutathione = L-ascorbate + glutathione disulfide.
glutathione transferase activity Catalysis of the reaction: R-X + glutathione = H-X + R-S-glutathione. R may be an aliphatic, aromatic or heterocyclic group; X may be a sulfate, nitrile or halide group.
methylarsonate reductase activity Catalysis of the reaction: 2 glutathione + H(+) + methylarsonate = glutathione disulfide + H(2)O + methylarsonous acid.
oxidoreductase activity Catalysis of an oxidation-reduction (redox) reaction, a reversible chemical reaction in which the oxidation state of an atom or atoms within a molecule is altered. One substrate acts as a hydrogen or electron donor and becomes oxidized, while the other acts as hydrogen or electron acceptor and becomes reduced.

9 GO annotations of biological process

Name Definition
cellular response to arsenic-containing substance Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arsenic stimulus from compounds containing arsenic, including arsenates, arsenites, and arsenides.
glutathione metabolic process The chemical reactions and pathways involving glutathione, the tripeptide glutamylcysteinylglycine, which acts as a coenzyme for some enzymes and as an antioxidant in the protection of sulfhydryl groups in enzymes and other proteins; it has a specific role in the reduction of hydrogen peroxide (H2O2) and oxidized ascorbate, and it participates in the gamma-glutamyl cycle.
L-ascorbic acid metabolic process The chemical reactions and pathways involving L-ascorbic acid, (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2,5-dihydrofuran-3-olate; L-ascorbic acid is vitamin C and has co-factor and anti-oxidant activities in many species.
negative regulation of ryanodine-sensitive calcium-release channel activity Any process that decreases the activity of a ryanodine-sensitive calcium-release channel. The ryanodine-sensitive calcium-release channel catalyzes the transmembrane transfer of a calcium ion by a channel that opens when a ryanodine class ligand has been bound by the channel complex or one of its constituent parts.
positive regulation of ryanodine-sensitive calcium-release channel activity Any process that increases the activity of a ryanodine-sensitive calcium-release channel. The ryanodine-sensitive calcium-release channel catalyzes the transmembrane transfer of a calcium ion by a channel that opens when a ryanodine class ligand has been bound by the channel complex or one of its constituent parts.
positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Any process that activates, maintains or increases the frequency, rate or extent of skeletal muscle contraction via the regulation of the release of sequestered calcium ion by sarcoplasmic reticulum into cytosol. The sarcoplasmic reticulum is the endoplasmic reticulum of striated muscle, specialised for the sequestration of calcium ions that are released upon receipt of a signal relayed by the T tubules from the neuromuscular junction.
regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion Any process that modulates the frequency, rate or extent of cardiac muscle contraction via the regulation of the release of sequestered calcium ion by sarcoplasmic reticulum into cytosol. The sarcoplasmic reticulum is the endoplasmic reticulum of striated muscle, specialised for the sequestration of calcium ions that are released upon receipt of a signal relayed by the T tubules from the neuromuscular junction.
regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum Any process that modulates the rate, frequency or extent of release of sequestered calcium ion into cytosol by the sarcoplasmic reticulum, the process in which the release of sequestered calcium ion by sarcoplasmic reticulum into cytosol occurs via calcium release channels.
xenobiotic catabolic process The chemical reactions and pathways resulting in the breakdown of a xenobiotic compound, a compound foreign to the organim exposed to it. It may be synthesized by another organism (like ampicilin) or it can be a synthetic chemical.

6 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
O09131 Gsto1 Glutathione S-transferase omega-1 Mus musculus (Mouse) PR
Q9N1F5 GSTO1 Glutathione S-transferase omega-1 Sus scrofa (Pig) PR
Q9Z339 Gsto1 Glutathione S-transferase omega-1 Rattus norvegicus (Rat) PR
P46421 GSTU5 Glutathione S-transferase U5 Arabidopsis thaliana (Mouse-ear cress) PR
Q9FUS9 GSTU18 Glutathione S-transferase U18 Arabidopsis thaliana (Mouse-ear cress) PR
Q9ZW30 GSTU1 Glutathione S-transferase U1 Arabidopsis thaliana (Mouse-ear cress) PR
10 20 30 40 50 60
MSGESARSLG KGSAPPGPVP EGSIRIYSMR FCPFAERTRL VLKAKGIRHE VININLKNKP
70 80 90 100 110 120
EWFFKKNPFG LVPVLENSQG QLIYESAITC EYLDEAYPGK KLLPDDPYEK ACQKMILELF
130 140 150 160 170 180
SKVPSLVGSF IRSQNKEDYA GLKEEFRKEF TKLEEVLTNK KTTFFGGNSI SMIDYLIWPW
190 200 210 220 230 240
FERLEAMKLN ECVDHTPKLK LWMAAMKEDP TVSALLTSEK DWQGFLELYL QNSPEACDYG
L