CPLM 1.0 - Compendium of Protein Lysine Modification
TagContent
CPLM ID CPLM-012201
UniProt Accession
Genbank Protein ID
Genbank Nucleotide ID
Protein Name
 Phorbol-12-myristate-13-acetate-induced protein 1 
Protein Synonyms/Alias
 PMA-induced protein 1; Immediate-early-response protein APR; Protein Noxa 
Gene Name
 PMAIP1 
Gene Synonyms/Alias
 NOXA 
Created Date
 July 27, 2013 
Organism
 Homo sapiens (Human) 
NCBI Taxa ID
 9606 
Lysine Modification
Position
Peptide
Type
References
35QLRRFGDKLNFRQKLubiquitination[1, 2, 3, 4, 5, 6, 7]
41DKLNFRQKLLNLISKubiquitination[2, 3, 4, 5, 6, 8]
48KLLNLISKLFCSGT*ubiquitination[3, 8, 9]
Reference
 [1] Mass spectrometric analysis of lysine ubiquitylation reveals promiscuity at site level.
 Danielsen JM, Sylvestersen KB, Bekker-Jensen S, Szklarczyk D, Poulsen JW, Horn H, Jensen LJ, Mailand N, Nielsen ML.
 Mol Cell Proteomics. 2011 Mar;10(3):M110.003590. [PMID: 21139048]
 [2] A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles.
 Wagner SA, Beli P, Weinert BT, Nielsen ML, Cox J, Mann M, Choudhary C.
 Mol Cell Proteomics. 2011 Oct;10(10):M111.013284. [PMID: 21890473]
 [3] Systematic and quantitative assessment of the ubiquitin-modified proteome.
 Kim W, Bennett EJ, Huttlin EL, Guo A, Li J, Possemato A, Sowa ME, Rad R, Rush J, Comb MJ, Harper JW, Gygi SP.
 Mol Cell. 2011 Oct 21;44(2):325-40. [PMID: 21906983]
 [4] Systems-wide analysis of ubiquitylation dynamics reveals a key role for PAF15 ubiquitylation in DNA-damage bypass.
 Povlsen LK, Beli P, Wagner SA, Poulsen SL, Sylvestersen KB, Poulsen JW, Nielsen ML, Bekker-Jensen S, Mailand N, Choudhary C.
 Nat Cell Biol. 2012 Oct;14(10):1089-98. [PMID: 23000965]
 [5] Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments.
 Udeshi ND, Svinkina T, Mertins P, Kuhn E, Mani DR, Qiao JW, Carr SA.
 Mol Cell Proteomics. 2013 Mar;12(3):825-31. [PMID: 23266961]
 [6] hCKSAAP_UbSite: improved prediction of human ubiquitination sites by exploiting amino acid pattern and properties.
 Chen Z, Zhou Y, Song J, Zhang Z.
 Biochim Biophys Acta. 2013 Aug;1834(8):1461-7. [PMID: 23603789]
 [7] Integrated proteomic analysis of post-translational modifications by serial enrichment.
 Mertins P, Qiao JW, Patel J, Udeshi ND, Clauser KR, Mani DR, Burgess MW, Gillette MA, Jaffe JD, Carr SA.
 Nat Methods. 2013 Jul;10(7):634-7. [PMID: 23749302]
 [8] Proteome-wide identification of ubiquitylation sites by conjugation of engineered lysine-less ubiquitin.
 Oshikawa K, Matsumoto M, Oyamada K, Nakayama KI.
 J Proteome Res. 2012 Feb 3;11(2):796-807. [PMID: 22053931]
 [9] Global analysis of lysine ubiquitination by ubiquitin remnant immunoaffinity profiling.
 Xu G, Paige JS, Jaffrey SR.
 Nat Biotechnol. 2010 Aug;28(8):868-73. [PMID: 20639865
Functional Description
 Promotes activation of caspases and apoptosis. Promotes mitochondrial membrane changes and efflux of apoptogenic proteins from the mitochondria. Contributes to p53/TP53-dependent apoptosis after radiation exposure. Promotes proteasomal degradation of MCL1. Competes with BAK1 for binding to MCL1 and can displace BAK1 from its binding site on MCL1 (By similarity). Competes with BIM/BCL2L11 for binding to MCL1 and can displace BIM/BCL2L11 from its binding site on MCL1. 
Sequence Annotation
 REGION 41 50 Required for mitochondrial location.
 MOTIF 29 37 BH3.  
Keyword
 3D-structure; Apoptosis; Complete proteome; Mitochondrion; Reference proteome. 
Sequence Source
 UniProt (SWISSPROT/TrEMBL); GenBank; EMBL 
Protein Length
 54 AA 
Protein Sequence
MPGKKARKNA QPSPARAPAE LEVECATQLR RFGDKLNFRQ KLLNLISKLF CSGT 54 
Gene Ontology
 GO:0005829; C:cytosol; IDA:UniProtKB.
 GO:0005741; C:mitochondrial outer membrane; TAS:Reactome.
 GO:0005634; C:nucleus; IDA:UniProtKB.
 GO:0006919; P:activation of cysteine-type endopeptidase activity involved in apoptotic process; IDA:HGNC.
 GO:0006921; P:cellular component disassembly involved in execution phase of apoptosis; IDA:HGNC.
 GO:0042149; P:cellular response to glucose starvation; IMP:UniProtKB.
 GO:0071456; P:cellular response to hypoxia; IEP:UniProtKB.
 GO:0006917; P:induction of apoptosis; IDA:UniProtKB.
 GO:0072332; P:intrinsic apoptotic signaling pathway by p53 class mediator; IMP:UniProtKB.
 GO:0048147; P:negative regulation of fibroblast proliferation; IEA:Compara.
 GO:0010917; P:negative regulation of mitochondrial membrane potential; ISS:UniProtKB.
 GO:0043517; P:positive regulation of DNA damage response, signal transduction by p53 class mediator; IMP:UniProtKB.
 GO:0010907; P:positive regulation of glucose metabolic process; IDA:UniProtKB.
 GO:2001244; P:positive regulation of intrinsic apoptotic signaling pathway; IDA:UniProtKB.
 GO:0043525; P:positive regulation of neuron apoptotic process; IEA:Compara.
 GO:1900740; P:positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway; TAS:Reactome.
 GO:0032461; P:positive regulation of protein oligomerization; IDA:UniProtKB.
 GO:0090200; P:positive regulation of release of cytochrome c from mitochondria; IDA:UniProtKB.
 GO:0010498; P:proteasomal protein catabolic process; IDA:UniProtKB.
 GO:0072593; P:reactive oxygen species metabolic process; IDA:UniProtKB.
 GO:0046902; P:regulation of mitochondrial membrane permeability; IDA:UniProtKB.
 GO:0001836; P:release of cytochrome c from mitochondria; IEA:Compara.
 GO:0006974; P:response to DNA damage stimulus; IEA:Compara.
 GO:0043331; P:response to dsRNA; IDA:HGNC.
 GO:0009411; P:response to UV; IEA:Compara.
 GO:0010165; P:response to X-ray; IEA:Compara.
 GO:0043029; P:T cell homeostasis; ISS:UniProtKB.
 GO:0006926; P:virus-infected cell apoptotic process; IDA:HGNC. 
Interpro
 IPR024140; PMA-induced_Noxa. 
Pfam
  
SMART
  
PROSITE
 PS01259; BH3 
PRINTS