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

2 structures for Q7Z7E8

Entry ID Method Resolution Chain Position Source
2QGX X-ray 256 A A/B/C/D 247-414 PDB
AF-Q7Z7E8-F1 Predicted AlphaFoldDB

176 variants for Q7Z7E8

Variant ID(s) Position Change Description Diseaes Association Provenance
rs971266222
CA30822557
6 P>Q No ClinGen
TOPMed
rs771152409
CA1130573
11 Q>L No ClinGen
ExAC
CA342628945
rs1184846428
12 P>A No ClinGen
TOPMed
CA342628941
rs1453369815
12 P>L No ClinGen
TOPMed
gnomAD
rs1453369815
CA342628942
12 P>R No ClinGen
TOPMed
gnomAD
rs1402375108
CA342628929
14 P>L No ClinGen
TOPMed
CA342628931
rs1402375108
14 P>Q No ClinGen
TOPMed
rs1318819764
CA342628925
15 G>A No ClinGen
TOPMed
CA342628913
rs1371343835
16 Q>H No ClinGen
TOPMed
CA342628915
rs1294741983
16 Q>L No ClinGen
TOPMed
rs1439647371
CA342628889
18 L>R No ClinGen
TOPMed
rs1225993830
CA342628881
19 G>E No ClinGen
TOPMed
rs1251189872
CA342628883
19 G>W No ClinGen
TOPMed
gnomAD
CA342628859
rs1285649866
21 Q>R No ClinGen
TOPMed
rs917971089
CA30822550
22 G>R No ClinGen
TOPMed
gnomAD
rs1213787886
CA342628821
24 A>V No ClinGen
TOPMed
rs1254911006
CA342628810
25 P>R No ClinGen
TOPMed
CA342628795
rs1326049244
26 G>E No ClinGen
TOPMed
gnomAD
rs992248839
CA30822547
26 G>R No ClinGen
TOPMed
CA30822539
rs959485135
27 A>S No ClinGen
TOPMed
TCGA novel 27 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA342628785
rs1407571668
27 A>V No ClinGen
TOPMed
gnomAD
CA342628782
rs1221282076
28 G>R No ClinGen
gnomAD
CA342628752
rs1398856343
30 G>D No ClinGen
TOPMed
rs549444803
CA30822469
32 G>A No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA1130569
rs549444803
32 G>E No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA30822484
rs778022056
CA1130570
32 G>R No ClinGen
ExAC
TOPMed
gnomAD
rs549444803
CA1130568
32 G>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1448704725
CA342628378
33 G>A No ClinGen
gnomAD
CA1130567
CA30822459
rs755410020
33 G>R No ClinGen
ExAC
TOPMed
gnomAD
rs755410020
CA1130566
33 G>W No ClinGen
ExAC
TOPMed
gnomAD
rs759160193 34 G>A Variant assessed as Somatic; 0.0007761 impact. [NCI-TCGA] No NCI-TCGA
CA342628374
rs752073705
34 G>C No ClinGen
ExAC
TOPMed
gnomAD
CA342628373
rs752073705
34 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA1130565
rs752073705
34 G>S No ClinGen
ExAC
TOPMed
gnomAD
rs1469467683
CA342628365
34 G>V No ClinGen
gnomAD
CA342628361
rs1189896763
35 P>A No ClinGen
TOPMed
CA1130562
rs765835407
35 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA342628342
rs1161574903
36 G>A No ClinGen
gnomAD
rs1356816076
CA342628330
37 P>L No ClinGen
gnomAD
CA342628335
rs1241942353
37 P>S No ClinGen
TOPMed
gnomAD
CA342628328
rs1571012636
38 G>R No ClinGen
Ensembl
CA342628303
rs1295712310
40 C>S No ClinGen
TOPMed
rs1463087988
CA342628281
42 R>K No ClinGen
gnomAD
CA342628274
rs1241671911
42 R>S No ClinGen
gnomAD
TCGA novel 43 R>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 43 R>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA342628217
rs1260887468
48 L>V No ClinGen
gnomAD
CA342628069
rs775595854
67 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA342628049
rs1185228904
70 S>I No ClinGen
TOPMed
TCGA novel 74 L>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs772172320
CA1130553
76 A>P No ClinGen
ExAC
gnomAD
CA1130552
rs369150212
78 A>D No ClinGen
ESP
ExAC
gnomAD
TCGA novel 79 G>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1475538185
CA342627987
80 G>V No ClinGen
TOPMed
rs1446972119
CA342627984
81 A>T No ClinGen
gnomAD
rs773220291
CA342627975
82 G>A No ClinGen
ExAC
TOPMed
gnomAD
CA30822358
rs376201812
82 G>R No ClinGen
ESP
TOPMed
gnomAD
rs773220291
CA1130551
82 G>V No ClinGen
ExAC
TOPMed
gnomAD
CA342627973
rs1264335540
83 A>T No ClinGen
TOPMed
gnomAD
CA342627969
rs1414651090
83 A>V No ClinGen
TOPMed
rs1484714830
CA342627960
85 A>S No ClinGen
TOPMed
gnomAD
rs202059318
CA1130549
86 A>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA342627956
rs202059318
86 A>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA342627949
rs1360996342
87 P>S No ClinGen
TOPMed
gnomAD
CA342627943
rs1340300733
88 G>R No ClinGen
TOPMed
rs747413918
CA1130546
89 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA1130547
rs375766283
89 P>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 90 H>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1485319244
CA342627925
91 L>F No ClinGen
TOPMed
CA342627923
rs1297518207
91 L>P No ClinGen
gnomAD
TCGA novel 91 L>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA30822319
rs917087614
92 P>S No ClinGen
TOPMed
gnomAD
TCGA novel 93 P>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs372729486
CA1130542
93 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA1130540
rs372729486
93 P>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA1130541
rs372729486
93 P>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs749948005
CA342627915
93 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs749948005
CA1130543
93 P>T No ClinGen
ExAC
TOPMed
gnomAD
CA342627913
rs1434648674
94 R>L No ClinGen
TOPMed
CA1130538
rs760511660
94 R>W No ClinGen
ExAC
gnomAD
rs200884226
CA1130537
95 G>E No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs200884226
CA1130536
95 G>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA342627901
rs1191555387
96 S>L No ClinGen
gnomAD
rs773274880
CA1130534
98 P>S No ClinGen
ExAC
gnomAD
CA1130533
rs769776532
99 G>V No ClinGen
ExAC
gnomAD
rs979819603
CA30822224
105 H>Y No ClinGen
TOPMed
rs1443321482
COSM332343
CA342627832
107 N>S lung [Cosmic] No ClinGen
cosmic curated
TOPMed
rs1179106875
CA342627233
110 E>Q No ClinGen
gnomAD
TCGA novel 113 P>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 114 A>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1426692240
CA342627066
115 V>A No ClinGen
gnomAD
CA1130503
rs777494406
116 P>R No ClinGen
ExAC
gnomAD
TCGA novel 135 L>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA342626396
rs1295887242
135 L>P No ClinGen
TOPMed
rs201163919
CA1130500
136 V>G No ClinGen
ExAC
gnomAD
rs1262680395
CA342626358
137 D>E No ClinGen
gnomAD
CA1130498
rs751419079
137 D>G No ClinGen
ExAC
gnomAD
CA342626362
rs751419079
137 D>V No ClinGen
ExAC
gnomAD
CA1130497
rs766212921
138 I>K No ClinGen
ExAC
rs1352036938
CA342626338
138 I>M No ClinGen
gnomAD
rs1002897010
CA30820465
138 I>V No ClinGen
TOPMed
TCGA novel 139 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs753847447
CA1130495
140 K>E No ClinGen
ExAC
gnomAD
CA1130494
rs764169973
144 L>V No ClinGen
ExAC
gnomAD
CA30820067
rs200287421
153 I>V No ClinGen
Ensembl
CA1130467
rs766865464
168 V>L No ClinGen
ExAC
gnomAD
CA342625494
rs1199621876
169 E>K No ClinGen
gnomAD
rs1231969743
CA342625409
172 D>E No ClinGen
TOPMed
rs1274144160
CA342625389
173 Q>H No ClinGen
TOPMed
gnomAD
CA342625343
rs1553202293
176 P>T No ClinGen
Ensembl
CA342625325
rs1489252477
177 A>T No ClinGen
gnomAD
CA342625285
rs1216621205
179 Q>E No ClinGen
gnomAD
rs560359173
CA1130439
180 C>R No ClinGen
1000Genomes
ExAC
gnomAD
CA342625147
rs1571009740
181 T>R No ClinGen
Ensembl
CA342625135
rs1226768476
182 Q>E No ClinGen
TOPMed
CA1130437
rs372396696
CA1130436
184 D>E Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
TOPMed
gnomAD
NCI-TCGA
rs770709805
CA1130438
184 D>N No ClinGen
ExAC
gnomAD
CA1130434
rs751729278
185 V>M No ClinGen
ExAC
TOPMed
gnomAD
rs766654924
CA30819517
193 E>G No ClinGen
Ensembl
CA342624504
rs1277200902
198 T>R No ClinGen
TOPMed
TCGA novel 199 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1217221602
CA342624450
200 D>E No ClinGen
TOPMed
CA30818098
rs1042067027
200 D>G No ClinGen
TOPMed
CA342624472
rs1290868665
200 D>Y No ClinGen
gnomAD
TCGA novel 208 E>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA1130412
rs142718155
209 E>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 210 E>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs528168401
CA1130408
212 A>P No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA1130409
rs528168401
212 A>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA342624019
rs764645047
214 G>D No ClinGen
ExAC
gnomAD
CA1130407
rs764645047
214 G>V No ClinGen
ExAC
gnomAD
CA342623934
rs1361589333
218 E>D No ClinGen
TOPMed
gnomAD
CA342623605
rs1378027309
228 A>V No ClinGen
TOPMed
rs1170803831
CA342623219
235 K>R No ClinGen
TOPMed
rs373938647
CA1130401
243 N>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA1130400
rs762787582
243 N>S No ClinGen
ExAC
gnomAD
rs771114797
CA1130371
245 A>T No ClinGen
ExAC
gnomAD
rs1313474576
CA342622667
245 A>V No ClinGen
TOPMed
rs770403490
CA30817562
246 V>M No ClinGen
Ensembl
TCGA novel 252 A>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA30817537
rs894189614
262 D>V No ClinGen
Ensembl
CA342621981
rs1318409304
263 I>T No ClinGen
TOPMed
rs1274387760
CA342622000
263 I>V No ClinGen
gnomAD
rs781649844
CA1130366
265 R>Q No ClinGen
ExAC
gnomAD
CA1130365
rs755537885
271 G>D No ClinGen
ExAC
gnomAD
COSM206573
rs1360882504
CA342621442
277 E>K lung Variant assessed as Somatic; 0.0 impact. large_intestine endometrium breast [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs763990597
CA1130337
279 V>M No ClinGen
ExAC
gnomAD
rs1356115562
CA342621382
280 N>S No ClinGen
gnomAD
CA1130318
rs755837391
301 N>D No ClinGen
ExAC
gnomAD
CA30816850
rs372294769
301 N>S No ClinGen
gnomAD
TCGA novel 302 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA342620018
rs1244213945
304 Q>H No ClinGen
gnomAD
rs200026897
CA1130315
307 K>N No ClinGen
ExAC
TOPMed
gnomAD
CA342619796
rs1239330949
312 A>G No ClinGen
TOPMed
rs1197670799
CA342619771
313 D>A No ClinGen
gnomAD
rs1255718672
COSM3418105
CA342619788
313 D>N Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs1415885886
CA342619714
315 I>V No ClinGen
TOPMed
CA342619658
rs1217405716
317 L>F No ClinGen
gnomAD
rs760934058
CA1130309
322 K>I No ClinGen
ExAC
gnomAD
CA342619506
rs760934058
322 K>T No ClinGen
ExAC
gnomAD
rs780802766
CA1130276
334 V>F No ClinGen
ExAC
gnomAD
CA1130275
rs768464949
336 S>A No ClinGen
ExAC
gnomAD
CA342618937
rs1482624334
340 S>C No ClinGen
gnomAD
rs1263328847
CA342618899
341 G>E No ClinGen
gnomAD
CA1130256
rs779824604
358 Q>* No ClinGen
ExAC
gnomAD
CA342617599
rs1202188337
370 I>V No ClinGen
gnomAD
CA342616462
rs1279374126
395 L>V No ClinGen
Ensembl
TCGA novel 396 T>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1414307245
CA342616296
399 Q>E No ClinGen
gnomAD
rs779158559
CA1130207
404 S>F No ClinGen
ExAC
gnomAD
CA1130205
rs754369992
410 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1415370636 412 N>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 413 G>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs771165587
CA1130184
415 Y>D No ClinGen
ExAC
gnomAD
CA1130183
rs749699818
417 P>L No ClinGen
ExAC
gnomAD

No associated diseases with Q7Z7E8

No regional properties for Q7Z7E8

Type Name Position InterPro Accession
No domain, repeats, and functional sites for Q7Z7E8

Functions

Description
EC Number 2.3.2.23 Aminoacyltransferases
Subcellular Localization
  • Nucleus
  • Cell projection, filopodium
  • Cytoplasm, cytosol
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

3 GO annotations of cellular component

Name Definition
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
filopodium Thin, stiff, actin-based protrusion extended by the leading edge of a motile cell such as a crawling fibroblast or amoeba, or an axonal or dendritic growth cone, or a dendritic shaft.
nucleus A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent.

2 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
ubiquitin conjugating enzyme activity Isoenergetic transfer of ubiquitin from one protein to another via the reaction X-ubiquitin + Y -> Y-ubiquitin + X, where both the X-ubiquitin and Y-ubiquitin linkages are thioester bonds between the C-terminal glycine of ubiquitin and a sulfhydryl side group of a cysteine residue.

7 GO annotations of biological process

Name Definition
embryo implantation Attachment of the blastocyst to the uterine lining.
fertilization The union of gametes of opposite sexes during the process of sexual reproduction to form a zygote. It involves the fusion of the gametic nuclei (karyogamy) and cytoplasm (plasmogamy).
mating behavior The behavioral interactions between organisms for the purpose of mating, or sexual reproduction resulting in the formation of zygotes.
prolactin secretion The regulated release of prolactin, a peptide hormone that stimulates lactation, from secretory granules in the anterior pituitary.
protein polyubiquitination Addition of multiple ubiquitin groups to a protein, forming a ubiquitin chain.
reproductive system development The progression of the reproductive system over time from its formation to the mature structure. The reproductive system consists of the organs that function in reproduction.
suckling behavior Specific behavior of a newborn or infant mammal that results in the derivation of nourishment from the breast.

13 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q32L27 UBE2Q2 Ubiquitin-conjugating enzyme E2 Q2 Bos taurus (Bovine) PR
Q9H8T0 AKTIP AKT-interacting protein Homo sapiens (Human) PR
Q9Y385 UBE2J1 Ubiquitin-conjugating enzyme E2 J1 Homo sapiens (Human) PR
P61086 UBE2K Ubiquitin-conjugating enzyme E2 K Homo sapiens (Human) PR
Q9NPD8 UBE2T Ubiquitin-conjugating enzyme E2 T Homo sapiens (Human) PR
O00762 UBE2C Ubiquitin-conjugating enzyme E2 C Homo sapiens (Human) PR
O14933 UBE2L6 Ubiquitin/ISG15-conjugating enzyme E2 L6 Homo sapiens (Human) PR
Q96LR5 UBE2E2 Ubiquitin-conjugating enzyme E2 E2 Homo sapiens (Human) PR
Q969T4 UBE2E3 Ubiquitin-conjugating enzyme E2 E3 Homo sapiens (Human) PR
A1L167 UBE2QL1 Ubiquitin-conjugating enzyme E2Q-like protein 1 Homo sapiens (Human) PR
Q16763 UBE2S Ubiquitin-conjugating enzyme E2 S Homo sapiens (Human) EV
A0PJN4 Ube2ql1 Ubiquitin-conjugating enzyme E2Q-like protein 1 Mus musculus (Mouse) PR
Q7TSS2 Ube2q1 Ubiquitin-conjugating enzyme E2 Q1 Mus musculus (Mouse) PR
10 20 30 40 50 60
MQQPQPQGQQ QPGPGQQLGG QGAAPGAGGG PGGGPGPGPC LRRELKLLES IFHRGHERFR
70 80 90 100 110 120
IASACLDELS CEFLLAGAGG AGAGAAPGPH LPPRGSVPGD PVRIHCNITE SYPAVPPIWS
130 140 150 160 170 180
VESDDPNLAA VLERLVDIKK GNTLLLQHLK RIISDLCKLY NLPQHPDVEM LDQPLPAEQC
190 200 210 220 230 240
TQEDVSSEDE DEEMPEDTED LDHYEMKEEE PAEGKKSEDD GIGKENLAIL EKIKKNQRQD
250 260 270 280 290 300
YLNGAVSGSV QATDRLMKEL RDIYRSQSFK GGNYAVELVN DSLYDWNVKL LKVDQDSALH
310 320 330 340 350 360
NDLQILKEKE GADFILLNFS FKDNFPFDPP FVRVVSPVLS GGYVLGGGAI CMELLTKQGW
370 380 390 400 410 420
SSAYSIESVI MQISATLVKG KARVQFGANK SQYSLTRAQQ SYKSLVQIHE KNGWYTPPKE
DG