CPLM 1.0 - Compendium of Protein Lysine Modification
TagContent
CPLM ID CPLM-016850
UniProt Accession
Genbank Protein ID
Genbank Nucleotide ID
Protein Name
 Lon protease homolog, mitochondrial 
Protein Synonyms/Alias
 Lon protease-like protein; LONP; Mitochondrial ATP-dependent protease Lon; Serine protease 15 
Gene Name
 Lonp1 
Gene Synonyms/Alias
 Prss15 
Created Date
 July 27, 2013 
Organism
 Mus musculus (Mouse) 
NCBI Taxa ID
 10090 
Lysine Modification
Position
Peptide
Type
References
221GLEPEAEKQKSRRKLacetylation[1]
363KKEFELSKLQQRLGRacetylation[1, 2, 3]
363KKEFELSKLQQRLGRsuccinylation[3]
375LGREVEEKIKQTHRKacetylation[1]
382KIKQTHRKYLLQEQLacetylation[2]
400KKELGLEKDDKDAIEacetylation[1, 4]
409DKDAIEEKFRERLREacetylation[1, 4]
707NLQKQVEKVLRKAAYacetylation[1]
Reference
 [1] Calorie restriction and SIRT3 trigger global reprogramming of the mitochondrial protein acetylome.
 Hebert AS, Dittenhafer-Reed KE, Yu W, Bailey DJ, Selen ES, Boersma MD, Carson JJ, Tonelli M, Balloon AJ, Higbee AJ, Westphall MS, Pagliarini DJ, Prolla TA, Assadi-Porter F, Roy S, Denu JM, Coon JJ.
 Mol Cell. 2013 Jan 10;49(1):186-99. [PMID: 23201123]
 [2] Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways.
 Rardin MJ, Newman JC, Held JM, Cusack MP, Sorensen DJ, Li B, Schilling B, Mooney SD, Kahn CR, Verdin E, Gibson BW.
 Proc Natl Acad Sci U S A. 2013 Apr 16;110(16):6601-6. [PMID: 23576753]
 [3] SIRT5-Mediated Lysine Desuccinylation Impacts Diverse Metabolic Pathways.
 Park J, Chen Y, Tishkoff DX, Peng C, Tan M, Dai L, Xie Z, Zhang Y, Zwaans BM, Skinner ME, Lombard DB, Zhao Y.
 Mol Cell. 2013 Jun 27;50(6):919-30. [PMID: 23806337]
 [4] Quantification of mitochondrial acetylation dynamics highlights prominent sites of metabolic regulation.
 Still AJ, Floyd BJ, Hebert AS, Bingman CA, Carson JJ, Gunderson DR, Dolan BK, Grimsrud PA, Dittenhafer-Reed KE, Stapleton DS, Keller MP, Westphall MS, Denu JM, Attie AD, Coon JJ, Pagliarini DJ.
 J Biol Chem. 2013 Jul 17;. [PMID: 23864654
Functional Description
 ATP-dependent serine protease that mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides as well as certain short-lived regulatory proteins in the mitochondrial matrix. May also have a chaperone function in the assembly of inner membrane protein complexes. Participates in the regulation of mitochondrial gene expression and in the maintenance of the integrity of the mitochondrial genome. Binds to mitochondrial promoters and RNA in a single- stranded, site-specific, and strand-specific manner. May regulate mitochondrial DNA replication and/or gene expression using site- specific, single-stranded DNA binding to target the degradation of regulatory proteins binding to adjacent sites in mitochondrial promoters (By similarity). 
Sequence Annotation
 DOMAIN 112 357 Lon.
 NP_BIND 512 519 ATP (By similarity).
 ACT_SITE 844 844 By similarity.
 ACT_SITE 887 887 By similarity.  
Keyword
 ATP-binding; Complete proteome; Direct protein sequencing; DNA-binding; Hydrolase; Mitochondrion; Nucleotide-binding; Protease; Reference proteome; Serine protease; Transit peptide. 
Sequence Source
 UniProt (SWISSPROT/TrEMBL); GenBank; EMBL 
Protein Length
 949 AA 
Protein Sequence
MAASTGYVRL WAAARCWVLR RPLLAVTGGR VPSASGSWLR RGCRACDMSA PWGGRVLPGG 60
VQWRGLWDSG NRGGSDETSE GGAEDGATAS TGEGPVVTAL APMTVPDVFP HLPLIAITRN 120
PVFPRFIKIV EVKNKKLVEL LRRKVRLAQP YVGVFLKRDD NNESDVVESL DEIYHTGTFA 180
QIHEMQDLGD KLRMIVTGHR RIHISRQLEV EPEGLEPEAE KQKSRRKLKR GKKEVEDELG 240
PKPQLEMVTE AATDTSKEVL MVEVENVAHE DFQVTEEVKA LTAEIVKTIR DIIALNPLYR 300
ESVLQMMQAG QRVVDNPIYL SDMGAALTGA ESHELQDVLE ETNILKRLYK ALSLLKKEFE 360
LSKLQQRLGR EVEEKIKQTH RKYLLQEQLK IIKKELGLEK DDKDAIEEKF RERLRELVVP 420
KHVMDVVDEE LSKLALLDNH SSEFNVTRNY LDWLTSIPWG RQSDENLDLA RAQAVLEEDH 480
YGMEDVKKRV LEFIAVSQLR GSTQGKILCF HGPPGVGKTS IARSIARALG REYFRFSVGG 540
MTDVAEIKGH RRTYVGAMPG KIIQCLKKTK TENPLVLIDE VDKIGRGYQG DPSSALLELL 600
DPEQNANFLD HYLDVPVDLS KVLFICTANV IDTIPEPLRD RMEMINVSGY VAQEKLAIAE 660
RYLVPQARTL CGLDESKAQL SAAVLTLLIK QYCRESGVRN LQKQVEKVLR KAAYKIVSGE 720
AQTVQVTPEN LQDFVGKPVF TVERMYEVTP PGVVMGLAWT AMGGSTLFVE TSLRRPQPSG 780
SKEDKDGSLE VTGQLGDVMK ESARIAYTYA RAFLMEQDPE NDFLVTSHIH LHVPEGATPK 840
DGPSAGCTIV TALLSLALGQ PVLQNLAMTG EVSLTGKVLP VGGIKEKTIA AKRAGVTCII 900
LPAENRKDYS DLAPFITEGL EVHFVEHYRD IFPIAFPRRE HREALAVER 949 
Gene Ontology
 GO:0042645; C:mitochondrial nucleoid; IBA:RefGenome.
 GO:0043531; F:ADP binding; IEA:Compara.
 GO:0005524; F:ATP binding; IBA:RefGenome.
 GO:0004176; F:ATP-dependent peptidase activity; IDA:MGI.
 GO:0051880; F:G-quadruplex DNA binding; IEA:Compara.
 GO:0070361; F:mitochondrial light strand promoter anti-sense binding; IDA:MGI.
 GO:0043565; F:sequence-specific DNA binding; IEA:HAMAP.
 GO:0004252; F:serine-type endopeptidase activity; IBA:RefGenome.
 GO:0003697; F:single-stranded DNA binding; IDA:MGI.
 GO:0003727; F:single-stranded RNA binding; IBA:RefGenome.
 GO:0007568; P:aging; IEA:Compara.
 GO:0034599; P:cellular response to oxidative stress; IBA:RefGenome.
 GO:0051131; P:chaperone-mediated protein complex assembly; IBA:RefGenome.
 GO:0006515; P:misfolded or incompletely synthesized protein catabolic process; IBA:RefGenome.
 GO:0007005; P:mitochondrion organization; IBA:RefGenome.
 GO:0070407; P:oxidation-dependent protein catabolic process; IBA:RefGenome.
 GO:0051260; P:protein homooligomerization; IBA:RefGenome.
 GO:0090296; P:regulation of mitochondrial DNA replication; IEA:HAMAP.
 GO:0010044; P:response to aluminum ion; IEA:Compara.
 GO:0009725; P:response to hormone stimulus; IEA:Compara.
 GO:0001666; P:response to hypoxia; IBA:RefGenome. 
Interpro
 IPR003593; AAA+_ATPase.
 IPR003959; ATPase_AAA_core.
 IPR004815; Lon_bac/euk-typ.
 IPR027065; Lon_Prtase.
 IPR027503; lonm_euk.
 IPR027417; P-loop_NTPase.
 IPR008269; Pept_S16_C.
 IPR003111; Pept_S16_N.
 IPR008268; Peptidase_S16_AS.
 IPR015947; PUA-like_domain.
 IPR020568; Ribosomal_S5_D2-typ_fold.
 IPR014721; Ribosomal_S5_D2-typ_fold_subgr. 
Pfam
 PF00004; AAA
 PF02190; LON
 PF05362; Lon_C 
SMART
 SM00382; AAA
 SM00464; LON 
PROSITE
 PS01046; LON_SER 
PRINTS