UniProt:P0CG48 UBC

chain
  • chain:1-76
  • chain:77-152
  • chain:153-228
  • chain:229-304
  • chain:305-380
  • chain:381-456
  • chain:457-532
  • chain:533-608
  • chain:609-684
  • propeptide:-
checksum B6E7BC06FEE77196
comment
  • FUNCTION Exists either covalently attached to another protein, or free (unanchored). When covalently bound, it is conjugated to target proteins via an isopeptide bond either as a monomer (monoubiquitin), a polymer linked via different Lys residues of the ubiquitin (polyubiquitin chains) or a linear polymer linked via the initiator Met of the ubiquitin (linear polyubiquitin chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lys-6-linked may be involved in DNA repair; Lys-11-linked is involved in ERAD (endoplasmic reticulum-associated degradation) and in cell-cycle regulation; Lys-29-linked is involved in proteotoxic stress response and cell cycle; Lys-33-linked is involved in kinase modification; Lys-48-linked is involved in protein degradation via the proteasome; Lys-63-linked is involved in endocytosis, DNA-damage responses as well as in signaling processes leading to activation of the transcription factor NF-kappa-B. Linear polymer chains formed via attachment by the initiator Met lead to cell signaling. Ubiquitin is usually conjugated to Lys residues of target proteins, however, in rare cases, conjugation to Cys or Ser residues has been observed. When polyubiquitin is free (unanchored-polyubiquitin), it also has distinct roles, such as in activation of protein kinases, and in signaling.INTERACTION Phosphorylated at Ser-65 by PINK1 during mitophagy. Phosphorylated ubiquitin specifically binds and activates parkin (PRKN), triggering mitophagy (PubMed:24660806, PubMed:24751536, PubMed:24784582, PubMed:25527291). Phosphorylation does not affect E1-mediated E2 charging of ubiquitin but affects discharging of E2 enzymes to form polyubiquitin chains. It also affects deubiquitination by deubiquitinase enzymes such as USP30 (PubMed:25527291).PTM Mono-ADP-ribosylated at the C-terminus by PARP9, a component of the PPAR9-DTX3L complex. ADP-ribosylation requires processing by E1 and E2 enzymes and prevents ubiquitin conjugation to substrates such as histones.PTM (Microbial infection) Mono-ADP-ribosylated at Thr-66 by the C.violaceum CteC virulence factor. ADP-ribosylation causes the shutdown of polyubiquitin synthesis and disrupts the recognition and reversal of polyubiquitin.MISCELLANEOUS Ubiquitin is encoded by 4 different genes. UBA52 and RPS27A genes code for a single copy of ubiquitin fused to the ribosomal proteins eL40 and eS31, respectively. UBB and UBC genes code for a polyubiquitin precursor with exact head to tail repeats, the number of repeats differ between species and strains.MISCELLANEOUS For the sake of clarity sequence features are annotated only for the first chain, and are not repeated for each of the following chains.SIMILARITY Belongs to the ubiquitin family.
created [InstanceEdit:937368] Yung, CK
crossReference
databaseName UniProt
dbId 937372
description
  • recommendedName: Polyubiquitin-C component recommendedName: Ubiquitin /component
displayName UniProt:P0CG48 UBC
geneName
  • UBC
identifier P0CG48
isSequenceChanged false
keyword
  • 3D-structure
  • ADP-ribosylation
  • Cytoplasm
  • Direct protein sequencing
  • Isopeptide bond
  • Membrane
  • Mitochondrion
  • Mitochondrion outer membrane
  • Nucleus
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • Ubl conjugation
modified [InstanceEdit:12187927] Wright, Adam, 2024-03-12
name
  • UBC
otherIdentifier
  • 11744653_x_at
  • 11755503_x_at
  • 11758319_x_at
  • 1366_i_at
  • 1367_f_at
  • 16772172
  • 208980_PM_s_at
  • 208980_s_at
  • 211296_PM_x_at
  • 211296_x_at
  • 32334_f_at
  • 32335_r_at
  • 3476742
  • 3476743
  • 3476744
  • 3476745
  • 3476746
  • 3476747
  • 3476748
  • 3476749
  • 3476750
  • 3476751
  • 3476752
  • 3476753
  • 3476754
  • 3476755
  • 3476756
  • 3476757
  • 3476758
  • 3476759
  • 3476760
  • 3476761
  • 3476762
  • 3476763
  • 3476764
  • 3476765
  • 3476766
  • 3476767
  • 3476768
  • 3476769
  • 3476770
  • 3476771
  • 3476772
  • 3476773
  • 3476774
  • 3476775
  • 3476776
  • 3476777
  • 3476778
  • 7316
  • 7967563
  • A_23_P329740
  • A_24_P266880
  • GE519044
  • GO:0002020
  • GO:0003723
  • GO:0005515
  • GO:0005576
  • GO:0005615
  • GO:0005634
  • GO:0005654
  • GO:0005737
  • GO:0005739
  • GO:0005741
  • GO:0005768
  • GO:0005783
  • GO:0005789
  • GO:0005829
  • GO:0005886
  • GO:0010008
  • GO:0016020
  • GO:0016567
  • GO:0019941
  • GO:0030163
  • GO:0030666
  • GO:0031386
  • GO:0031410
  • GO:0031625
  • GO:0031982
  • GO:0036211
  • GO:0043226
  • GO:0070062
  • HMNXSV003045710
  • ILMN_1891922
  • ILMN_2038773
  • ILMN_2252160
  • ILMN_2331501
  • M26880_at
  • PH_hs_0006671
  • PH_hs_0030809
  • TC12002099.hg
  • g2647407_3p_a_at
  • g340067_3p_x_at
physicalEntity
referenceDatabase [ReferenceDatabase:2] UniProt
referenceGene
referenceTranscript
schemaClass ReferenceGeneProduct
secondaryIdentifier
  • UBC_HUMAN
  • P02248
  • P02249
  • P02250
  • P62988
  • Q29120
  • Q6LBL4
  • Q6LDU5
  • Q8WYN8
  • Q91887
  • Q91888
  • Q9BWD6
  • Q9BX98
  • Q9UEF2
  • Q9UEG1
  • Q9UEK8
  • Q9UPK7
sequenceLength 685
species [Species:48887] Homo sapiens
url https://purl.uniprot.org/uniprot/P0CG48

Referrals

(referenceEntity)
(referenceSequence)
(interactor)
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