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

8 structures for O00762

Entry ID Method Resolution Chain Position Source
1I7K X-ray 195 A A/B 1-179 PDB
4YII X-ray 180 A U 27-179 PDB
5A31 EM 430 A Q 29-173 PDB
5KHR EM 610 A Q 1-179 PDB
5L9U EM 640 A U 1-179 PDB
8TAR EM 400 A Q 29-173 PDB
8TAU EM 350 A Q 1-179 PDB
AF-O00762-F1 Predicted AlphaFoldDB

148 variants for O00762

Variant ID(s) Position Change Description Diseaes Association Provenance
CA409185301
rs1225528823
3 S>F No ClinGen
TOPMed
gnomAD
rs984421119
CA315616073
5 N>T No ClinGen
gnomAD
rs561525053
CA315616091
6 R>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA9880537
rs561525053
6 R>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs867231207
CA315616095
7 D>A No ClinGen
Ensembl
CA409185340
rs763421388
10 A>P No ClinGen
ExAC
TOPMed
gnomAD
rs763421388
CA9880539
10 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs763421388
CA315616099
10 A>T No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 11 T>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA409185349
rs1243957339
11 T>I No ClinGen
TOPMed
gnomAD
rs1202446446
CA409185346
11 T>S No ClinGen
TOPMed
gnomAD
rs1222721494
CA409185356
12 S>R No ClinGen
TOPMed
CA409185364
rs766882355
14 A>P No ClinGen
ExAC
TOPMed
gnomAD
rs766882355
CA409185365
14 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs766882355
CA9880540
14 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA409185366
rs1186759513
14 A>V No ClinGen
gnomAD
rs1392036860
CA409185369
15 A>T No ClinGen
gnomAD
rs1271204292
CA409185377
16 A>S No ClinGen
TOPMed
rs1429651798
CA409185380
16 A>V No ClinGen
gnomAD
rs774646356
CA9880541
17 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs774646356
CA409185382
17 R>G No ClinGen
ExAC
TOPMed
gnomAD
CA409185385
rs1376325872
17 R>L No ClinGen
gnomAD
rs1337052897
CA409185398
19 G>E No ClinGen
gnomAD
CA409185394
rs1467881661
19 G>R No ClinGen
gnomAD
CA409185401
rs1601038029
20 A>T No ClinGen
Ensembl
rs1387449323
CA409185414
22 P>S No ClinGen
gnomAD
CA9880543
rs11537645
23 S>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA409185428
rs761413591
24 G>R No ClinGen
ExAC
gnomAD
rs1368653521
CA409185430
24 G>V No ClinGen
TOPMed
rs761413591
CA9880545
24 G>W No ClinGen
ExAC
gnomAD
VAR_007694 25 G>D No UniProt
CA409185438
rs1386174145
26 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs749925974
CA9880548
27 A>P No ClinGen
ExAC
TOPMed
gnomAD
CA409185444
rs749925974
27 A>S No ClinGen
ExAC
TOPMed
gnomAD
CA9880547
rs749925974
27 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs1223889210
CA409185449
28 R>W No ClinGen
gnomAD
rs1267182417
CA409185467
31 V>L No ClinGen
TOPMed
gnomAD
rs1267182417
CA409185465
31 V>M No ClinGen
TOPMed
gnomAD
CA409185474
rs1356214083
32 G>D No ClinGen
TOPMed
gnomAD
rs1207003316
CA409185471
32 G>S No ClinGen
gnomAD
CA409185475
rs1356214083
32 G>V No ClinGen
TOPMed
gnomAD
rs761500077
CA9880565
36 Q>E No ClinGen
ExAC
TOPMed
gnomAD
rs1190657829
CA409185517
37 Q>* No ClinGen
gnomAD
rs1258952908
CA409185523
38 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs1207386492
CA409185532
39 L>V No ClinGen
TOPMed
CA409185543
rs1269104737
40 M>I No ClinGen
TOPMed
rs138058971
CA9880566
40 M>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA409185549
rs1423586972
41 T>I Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA409185547
rs1423586972
41 T>N No ClinGen
gnomAD
rs1223941923
CA409185558
43 M>L No ClinGen
gnomAD
rs545175408
CA9880567
43 M>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA409185557
rs1223941923
43 M>V No ClinGen
gnomAD
CA9880588
rs766016081
47 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA409185647
rs1189026288
54 P>S No ClinGen
TOPMed
CA315617320
rs377081477
56 S>* No ClinGen
ESP
TOPMed
rs144831911
CA9880589
57 D>N No ClinGen
1000Genomes
ExAC
gnomAD
CA9880590
rs759589512
59 L>F No ClinGen
ExAC
TOPMed
gnomAD
CA409185688
rs1174298561
60 F>S No ClinGen
gnomAD
rs767562250
CA9880591
62 W>C No ClinGen
ExAC
gnomAD
CA9880592
rs752601468
64 G>A No ClinGen
ExAC
gnomAD
CA409185731
rs1225404499
66 I>M No ClinGen
TOPMed
CA409185733
rs1319994180
67 H>D No ClinGen
gnomAD
CA409185737
rs1433546288
67 H>Q No ClinGen
gnomAD
CA315617334
rs956674941
67 H>R No ClinGen
TOPMed
gnomAD
rs1319994180
CA409185734
67 H>Y No ClinGen
gnomAD
CA409185750
rs1271262675
69 A>V No ClinGen
gnomAD
rs779653538
CA9880649
73 V>L No ClinGen
ExAC
gnomAD
rs746495033
CA9880650
74 Y>* No ClinGen
ExAC
gnomAD
rs768695868
CA9880651
75 E>D No ClinGen
ExAC
gnomAD
rs1448910805
CA409186132
77 L>P No ClinGen
gnomAD
CA9880652
rs547850953
78 R>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA9880653
rs761667583
79 Y>F No ClinGen
ExAC
TOPMed
gnomAD
CA9880654
rs769604009
80 K>* No ClinGen
ExAC
gnomAD
rs772939191
CA9880655
80 K>N No ClinGen
ExAC
gnomAD
rs763209065
CA9880656
82 S>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA9880658
rs751722028
84 E>D No ClinGen
ExAC
TOPMed
gnomAD
rs371616231
CA9880660
86 P>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs759551578
CA9880659
86 P>T No ClinGen
ExAC
gnomAD
CA9880661
rs753288094
87 S>G No ClinGen
ExAC
TOPMed
gnomAD
CA9880662
rs756640882
87 S>R No ClinGen
ExAC
gnomAD
CA9880664
rs754226233
89 Y>* No ClinGen
ExAC
rs778333049
CA9880663
89 Y>S No ClinGen
ExAC
gnomAD
rs374439898
CA315618202
90 P>A No ClinGen
ESP
rs758135325
CA9880665
92 N>S No ClinGen
ExAC
TOPMed
gnomAD
rs367706641
CA9880668
95 T>A No ClinGen
ESP
ExAC
gnomAD
rs367706641
CA409186238
95 T>S No ClinGen
ESP
ExAC
gnomAD
CA9880669
rs780709357
96 V>M No ClinGen
ExAC
gnomAD
CA9880671
rs769693911
97 K>N No ClinGen
ExAC
gnomAD
CA315618220
rs976266522
97 K>R No ClinGen
TOPMed
CA409186268
rs1198408107
100 T>A No ClinGen
gnomAD
CA9880672
COSM1027285
rs773029038
100 T>M Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA409186278
rs1254022907
101 P>L No ClinGen
TOPMed
gnomAD
rs932190109
CA315618263
103 Y>F No ClinGen
TOPMed
gnomAD
rs770704295
CA409186312
106 N>I No ClinGen
ExAC
TOPMed
gnomAD
CA9880676
rs770704295
106 N>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA9880678
rs759764860
107 V>M No ClinGen
ExAC
TOPMed
gnomAD
rs1225682574
CA409186331
109 T>N No ClinGen
gnomAD
CA9880679
rs767520518
111 G>D No ClinGen
ExAC
gnomAD
rs761307294
CA9880683
115 L>P No ClinGen
ExAC
gnomAD
CA9880684
rs764691584
121 K>T No ClinGen
ExAC
gnomAD
CA315618299
rs1033161095
122 W>R No ClinGen
Ensembl
rs1244942351
CA409186433
124 A>S No ClinGen
TOPMed
TCGA novel 124 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA9880686
COSM188841
rs757572822
125 L>P large_intestine Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs757572822
CA9880687
125 L>Q No ClinGen
ExAC
TOPMed
gnomAD
rs148799246
CA9880690
126 Y>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA9880689
rs148799246
126 Y>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA315618344
rs7352110
129 R>G No ClinGen
Ensembl
rs371311367
CA409186469
130 T>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs371311367
CA9880692
130 T>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA315618347
rs201176918
131 I>M No ClinGen
1000Genomes
rs767584548
CA315618348
133 L>F No ClinGen
Ensembl
rs777703076
CA9880693
136 Q>R No ClinGen
ExAC
TOPMed
gnomAD
CA315618357
rs902257654
138 L>F No ClinGen
TOPMed
rs1163401493
CA409186528
140 G>E No ClinGen
TOPMed
CA315618441
rs1036918950
141 E>D No ClinGen
Ensembl
rs1313636957
CA409186555
142 P>R No ClinGen
gnomAD
rs142378082
CA315618445
145 D>N No ClinGen
ESP
TOPMed
gnomAD
rs1274157914
CA409186591
146 S>N No ClinGen
gnomAD
CA409186622
rs1272519354
150 T>K No ClinGen
gnomAD
CA9880719
rs201125748
154 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs1198011557
CA409186654
155 L>I No ClinGen
TOPMed
CA9880720
rs776802939
156 W>R No ClinGen
ExAC
gnomAD
rs762275535
CA9880721
157 K>E No ClinGen
ExAC
TOPMed
gnomAD
rs770303252
CA9880722
157 K>R No ClinGen
ExAC
gnomAD
CA409186678
CA9880723
rs61760191
158 N>K No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
TCGA novel 158 N>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA9880724
rs763391914
159 P>T No ClinGen
ExAC
gnomAD
rs373084608
CA9880725
160 T>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA409186704
rs774676127
161 A>G No ClinGen
ExAC
TOPMed
gnomAD
rs752378234
CA9880726
161 A>P No ClinGen
ExAC
TOPMed
gnomAD
rs752378234
CA409186689
161 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA9880744
rs774676127
161 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA409186734
rs1318325554
165 Y>F No ClinGen
gnomAD
CA409186743
rs753350058
167 Q>* No ClinGen
ExAC
gnomAD
CA9880747
rs753350058
167 Q>E No ClinGen
ExAC
gnomAD
rs1029457888
CA315619068
167 Q>R Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA9880748
rs761402285
168 E>K No ClinGen
ExAC
CA315619079
rs202149476
169 T>A No ClinGen
1000Genomes
CA409186755
rs202149476
169 T>P No ClinGen
1000Genomes
CA409186763
rs1568717224
170 Y>S No ClinGen
Ensembl
rs955166544
CA315619099
173 Q>* No ClinGen
TOPMed
gnomAD
CA9880750
rs376878469
174 V>G No ClinGen
ESP
ExAC
gnomAD
CA9880751
rs758357409
175 T>P No ClinGen
ExAC
gnomAD
CA409186809
rs1324101765
177 Q>* No ClinGen
TOPMed
gnomAD
rs766325761
CA9880752
177 Q>R No ClinGen
ExAC
gnomAD
CA409186820
rs1282135234
178 E>D No ClinGen
gnomAD
rs985255663
CA315619134
178 E>G No ClinGen
Ensembl

No associated diseases with O00762

2 regional properties for O00762

Type Name Position InterPro Accession
domain Ubiquitin-conjugating enzyme E2 30 - 175 IPR000608
active_site Ubiquitin-conjugating enzyme, active site 103 - 118 IPR023313

Functions

Description
EC Number 2.3.2.23 Aminoacyltransferases
Subcellular Localization
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

6 GO annotations of cellular component

Name Definition
anaphase-promoting complex A ubiquitin ligase complex that degrades mitotic cyclins and anaphase inhibitory protein, thereby triggering sister chromatid separation and exit from mitosis. Substrate recognition by APC occurs through degradation signals, the most common of which is termed the Dbox degradation motif, originally discovered in cyclin B.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
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.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
ubiquitin ligase complex A protein complex that includes a ubiquitin-protein ligase and enables ubiquitin protein ligase activity. The complex also contains other proteins that may confer substrate specificity on the complex.

5 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.
ubiquitin protein ligase activity Catalysis of the transfer of ubiquitin to a substrate protein via the reaction X-ubiquitin + S -> X + S-ubiquitin, where X is either an E2 or E3 enzyme, the X-ubiquitin linkage is a thioester bond, and the S-ubiquitin linkage is an amide bond: an isopeptide bond between the C-terminal glycine of ubiquitin and the epsilon-amino group of lysine residues in the substrate or, in the linear extension of ubiquitin chains, a peptide bond the between the C-terminal glycine and N-terminal methionine of ubiquitin residues.
ubiquitin-like protein ligase binding Binding to a ubiquitin-like protein ligase, such as ubiquitin-ligase.
ubiquitin-protein transferase activity Catalysis of the transfer of ubiquitin from one protein to another via the reaction X-Ub + Y --> Y-Ub + X, where both X-Ub and Y-Ub are covalent linkages.

12 GO annotations of biological process

Name Definition
anaphase-promoting complex-dependent catabolic process The chemical reactions and pathways resulting in the breakdown of a protein or peptide by hydrolysis of its peptide bonds, initiated by the covalent attachment of ubiquitin, with ubiquitin-protein ligation catalyzed by the anaphase-promoting complex, and mediated by the proteasome.
cell division The process resulting in division and partitioning of components of a cell to form more cells; may or may not be accompanied by the physical separation of a cell into distinct, individually membrane-bounded daughter cells.
exit from mitosis The cell cycle transition where a cell leaves M phase and enters a new G1 phase. M phase is the part of the mitotic cell cycle during which mitosis and cytokinesis take place.
free ubiquitin chain polymerization The process of creating free ubiquitin chains, compounds composed of a large number of ubiquitin monomers. These chains are not conjugated to a protein.
positive regulation of exit from mitosis Any process that activates or increases the rate of progression from anaphase/telophase (high mitotic CDK activity) to G1 (low mitotic CDK activity).
positive regulation of ubiquitin protein ligase activity Any process that activates or increases the frequency, rate or extent of ubiquitin protein ligase activity.
protein K11-linked ubiquitination A protein ubiquitination process in which ubiquitin monomers are attached to a protein, and then ubiquitin polymers are formed by linkages between lysine residues at position 11 of the ubiquitin monomers. K11-linked polyubiquitination targets the substrate protein for degradation. The anaphase-promoting complex promotes the degradation of mitotic regulators by assembling K11-linked polyubiquitin chains.
protein K48-linked ubiquitination A protein ubiquitination process in which a polymer of ubiquitin, formed by linkages between lysine residues at position 48 of the ubiquitin monomers, is added to a protein. K48-linked ubiquitination targets the substrate protein for degradation.
protein polyubiquitination Addition of multiple ubiquitin groups to a protein, forming a ubiquitin chain.
protein ubiquitination The process in which one or more ubiquitin groups are added to a protein.
regulation of mitotic metaphase/anaphase transition Any process that modulates the frequency, rate or extent of the cell cycle process in which a cell progresses from metaphase to anaphase during mitosis, triggered by the activation of the anaphase promoting complex by Cdc20/Sleepy homolog which results in the degradation of Securin.
ubiquitin-dependent protein catabolic process The chemical reactions and pathways resulting in the breakdown of a protein or peptide by hydrolysis of its peptide bonds, initiated by the covalent attachment of a ubiquitin group, or multiple ubiquitin groups, to the protein.

12 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q32PA5 UBE2C Ubiquitin-conjugating enzyme E2 C 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
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
Q7Z7E8 UBE2Q1 Ubiquitin-conjugating enzyme E2 Q1 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
Q9D1C1 Ube2c Ubiquitin-conjugating enzyme E2 C Mus musculus (Mouse) PR
10 20 30 40 50 60
MASQNRDPAA TSVAAARKGA EPSGGAARGP VGKRLQQELM TLMMSGDKGI SAFPESDNLF
70 80 90 100 110 120
KWVGTIHGAA GTVYEDLRYK LSLEFPSGYP YNAPTVKFLT PCYHPNVDTQ GNICLDILKE
130 140 150 160 170
KWSALYDVRT ILLSIQSLLG EPNIDSPLNT HAAELWKNPT AFKKYLQETY SKQVTSQEP