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Database: UniProt
Entry: RM01_HUMAN
LinkDB: RM01_HUMAN
Original site: RM01_HUMAN 
ID   RM01_HUMAN              Reviewed;         325 AA.
AC   Q9BYD6; A6NG03; Q4W5B8; Q6IAG4; Q96BW3; Q9H793; Q9NRL5;
DT   17-OCT-2006, integrated into UniProtKB/Swiss-Prot.
DT   16-JUN-2009, sequence version 2.
DT   27-MAR-2024, entry version 168.
DE   RecName: Full=Large ribosomal subunit protein uL1m {ECO:0000303|PubMed:25278503};
DE   AltName: Full=39S ribosomal protein L1, mitochondrial;
DE            Short=L1mt;
DE            Short=MRP-L1;
DE   Flags: Precursor;
GN   Name=MRPL1; ORFNames=BM-022;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Bone marrow;
RA   Zhao M., Song H., Li N., Peng Y., Han Z., Chen Z.;
RT   "A novel gene expressed in human bone marrow.";
RL   Submitted (DEC-1999) to the EMBL/GenBank/DDBJ databases.
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=15815621; DOI=10.1038/nature03466;
RA   Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P.,
RA   Wagner-McPherson C., Layman D., Wylie K., Sekhon M., Becker M.C.,
RA   Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Kremitzki C., Oddy L.,
RA   Du H., Sun H., Bradshaw-Cordum H., Ali J., Carter J., Cordes M., Harris A.,
RA   Isak A., van Brunt A., Nguyen C., Du F., Courtney L., Kalicki J.,
RA   Ozersky P., Abbott S., Armstrong J., Belter E.A., Caruso L., Cedroni M.,
RA   Cotton M., Davidson T., Desai A., Elliott G., Erb T., Fronick C., Gaige T.,
RA   Haakenson W., Haglund K., Holmes A., Harkins R., Kim K., Kruchowski S.S.,
RA   Strong C.M., Grewal N., Goyea E., Hou S., Levy A., Martinka S., Mead K.,
RA   McLellan M.D., Meyer R., Randall-Maher J., Tomlinson C.,
RA   Dauphin-Kohlberg S., Kozlowicz-Reilly A., Shah N., Swearengen-Shahid S.,
RA   Snider J., Strong J.T., Thompson J., Yoakum M., Leonard S., Pearman C.,
RA   Trani L., Radionenko M., Waligorski J.E., Wang C., Rock S.M.,
RA   Tin-Wollam A.-M., Maupin R., Latreille P., Wendl M.C., Yang S.-P., Pohl C.,
RA   Wallis J.W., Spieth J., Bieri T.A., Berkowicz N., Nelson J.O., Osborne J.,
RA   Ding L., Meyer R., Sabo A., Shotland Y., Sinha P., Wohldmann P.E.,
RA   Cook L.L., Hickenbotham M.T., Eldred J., Williams D., Jones T.A., She X.,
RA   Ciccarelli F.D., Izaurralde E., Taylor J., Schmutz J., Myers R.M.,
RA   Cox D.R., Huang X., McPherson J.D., Mardis E.R., Clifton S.W., Warren W.C.,
RA   Chinwalla A.T., Eddy S.R., Marra M.A., Ovcharenko I., Furey T.S.,
RA   Miller W., Eichler E.E., Bork P., Suyama M., Torrents D., Waterston R.H.,
RA   Wilson R.K.;
RT   "Generation and annotation of the DNA sequences of human chromosomes 2 and
RT   4.";
RL   Nature 434:724-731(2005).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases.
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANTS LYS-47 AND SER-177.
RC   TISSUE=Bone marrow, and Skin;
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [MRNA] OF 10-325, AND SUBCELLULAR LOCATION.
RX   PubMed=11279069; DOI=10.1074/jbc.m100432200;
RA   Suzuki T., Terasaki M., Takemoto-Hori C., Hanada T., Ueda T., Wada A.,
RA   Watanabe K.;
RT   "Structural compensation for the deficit of rRNA with proteins in the
RT   mammalian mitochondrial ribosome. Systematic analysis of protein components
RT   of the large ribosomal subunit from mammalian mitochondria.";
RL   J. Biol. Chem. 276:21724-21736(2001).
RN   [6]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 23-325.
RA   Ebert L., Schick M., Neubert P., Schatten R., Henze S., Korn B.;
RT   "Cloning of human full open reading frames in Gateway(TM) system entry
RT   vector (pDONR201).";
RL   Submitted (JUN-2004) to the EMBL/GenBank/DDBJ databases.
RN   [7]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 68-325.
RC   TISSUE=Coronary artery;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [8]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RX   PubMed=21269460; DOI=10.1186/1752-0509-5-17;
RA   Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T.,
RA   Bennett K.L., Superti-Furga G., Colinge J.;
RT   "Initial characterization of the human central proteome.";
RL   BMC Syst. Biol. 5:17-17(2011).
RN   [9]
RP   NOMENCLATURE.
RX   PubMed=25278503; DOI=10.1126/science.1258026;
RA   Brown A., Amunts A., Bai X.C., Sugimoto Y., Edwards P.C., Murshudov G.,
RA   Scheres S.H., Ramakrishnan V.;
RT   "Structure of the large ribosomal subunit from human mitochondria.";
RL   Science 346:718-722(2014).
RN   [10]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RX   PubMed=25944712; DOI=10.1002/pmic.201400617;
RA   Vaca Jacome A.S., Rabilloud T., Schaeffer-Reiss C., Rompais M., Ayoub D.,
RA   Lane L., Bairoch A., Van Dorsselaer A., Carapito C.;
RT   "N-terminome analysis of the human mitochondrial proteome.";
RL   Proteomics 15:2519-2524(2015).
CC   -!- SUBUNIT: Component of the mitochondrial large ribosomal subunit (mt-
CC       LSU) (PubMed:11279069). Mature mammalian 55S mitochondrial ribosomes
CC       consist of a small (28S) and a large (39S) subunit. The 28S small
CC       subunit contains a 12S ribosomal RNA (12S mt-rRNA) and 30 different
CC       proteins. The 39S large subunit contains a 16S rRNA (16S mt-rRNA), a
CC       copy of mitochondrial valine transfer RNA (mt-tRNA(Val)), which plays
CC       an integral structural role, and 52 different proteins
CC       (PubMed:25278503). {ECO:0000250|UniProtKB:A6QPQ5,
CC       ECO:0000305|PubMed:11279069, ECO:0000305|PubMed:25278503}.
CC   -!- INTERACTION:
CC       Q9BYD6; Q9HD26: GOPC; NbExp=3; IntAct=EBI-5325394, EBI-349832;
CC       Q9BYD6; Q8N0X2-4: SPAG16; NbExp=3; IntAct=EBI-5325394, EBI-11946259;
CC       Q9BYD6; Q8N1B4: VPS52; NbExp=3; IntAct=EBI-5325394, EBI-2799833;
CC   -!- SUBCELLULAR LOCATION: Mitochondrion {ECO:0000250|UniProtKB:A6QPQ5,
CC       ECO:0000305|PubMed:11279069}.
CC   -!- SIMILARITY: Belongs to the universal ribosomal protein uL1 family.
CC       {ECO:0000305}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=AAF87327.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};
CC       Sequence=AAF87327.1; Type=Frameshift; Evidence={ECO:0000305};
CC       Sequence=AAH14356.1; Type=Erroneous initiation; Evidence={ECO:0000305};
CC       Sequence=AAH15109.1; Type=Erroneous initiation; Evidence={ECO:0000305};
CC       Sequence=AAH32595.1; Type=Erroneous initiation; Evidence={ECO:0000305};
CC       Sequence=AAY41057.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305};
CC       Sequence=BAB15005.1; Type=Erroneous initiation; Evidence={ECO:0000305};
CC       Sequence=BAB40180.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};
CC       Sequence=BAB40180.1; Type=Frameshift; Evidence={ECO:0000305};
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DR   EMBL; AF212225; AAF87327.1; ALT_SEQ; mRNA.
DR   EMBL; AC112225; AAY41057.1; ALT_SEQ; Genomic_DNA.
DR   EMBL; AC114801; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH471057; EAX05820.1; -; Genomic_DNA.
DR   EMBL; BC014356; AAH14356.1; ALT_INIT; mRNA.
DR   EMBL; BC015109; AAH15109.1; ALT_INIT; mRNA.
DR   EMBL; BC032595; AAH32595.1; ALT_INIT; mRNA.
DR   EMBL; AB049474; BAB40180.1; ALT_SEQ; mRNA.
DR   EMBL; CR457191; CAG33472.1; -; mRNA.
DR   EMBL; AK024791; BAB15005.1; ALT_INIT; mRNA.
DR   CCDS; CCDS3583.2; -.
DR   RefSeq; NP_064621.3; NM_020236.3.
DR   RefSeq; XP_011530500.1; XM_011532198.2.
DR   RefSeq; XP_011530501.1; XM_011532199.1.
DR   PDB; 7A5K; EM; 3.70 A; n=23-308.
DR   PDB; 7QI4; EM; 2.21 A; z=1-325.
DR   PDB; 7QI5; EM; 2.63 A; z=1-325.
DR   PDB; 7QI6; EM; 2.98 A; z=1-325.
DR   PDB; 8ANY; EM; 2.85 A; z=1-325.
DR   PDB; 8OIR; EM; 3.10 A; Bj=1-325.
DR   PDB; 8OIT; EM; 2.90 A; Bj=1-325.
DR   PDBsum; 7A5K; -.
DR   PDBsum; 7QI4; -.
DR   PDBsum; 7QI5; -.
DR   PDBsum; 7QI6; -.
DR   PDBsum; 8ANY; -.
DR   PDBsum; 8OIR; -.
DR   PDBsum; 8OIT; -.
DR   AlphaFoldDB; Q9BYD6; -.
DR   EMDB; EMD-11646; -.
DR   EMDB; EMD-13980; -.
DR   EMDB; EMD-13981; -.
DR   EMDB; EMD-13982; -.
DR   EMDB; EMD-15544; -.
DR   EMDB; EMD-16897; -.
DR   EMDB; EMD-16899; -.
DR   SMR; Q9BYD6; -.
DR   BioGRID; 122371; 200.
DR   ComplexPortal; CPX-5226; 39S mitochondrial large ribosomal subunit.
DR   CORUM; Q9BYD6; -.
DR   IntAct; Q9BYD6; 94.
DR   MINT; Q9BYD6; -.
DR   STRING; 9606.ENSP00000315017; -.
DR   GlyGen; Q9BYD6; 1 site, 1 O-linked glycan (1 site).
DR   iPTMnet; Q9BYD6; -.
DR   PhosphoSitePlus; Q9BYD6; -.
DR   SwissPalm; Q9BYD6; -.
DR   BioMuta; MRPL1; -.
DR   DMDM; 239938694; -.
DR   EPD; Q9BYD6; -.
DR   jPOST; Q9BYD6; -.
DR   MassIVE; Q9BYD6; -.
DR   MaxQB; Q9BYD6; -.
DR   PaxDb; 9606-ENSP00000315017; -.
DR   PeptideAtlas; Q9BYD6; -.
DR   ProteomicsDB; 79621; -.
DR   Pumba; Q9BYD6; -.
DR   Antibodypedia; 24877; 240 antibodies from 27 providers.
DR   DNASU; 65008; -.
DR   Ensembl; ENST00000315567.13; ENSP00000315017.8; ENSG00000169288.18.
DR   GeneID; 65008; -.
DR   KEGG; hsa:65008; -.
DR   MANE-Select; ENST00000315567.13; ENSP00000315017.8; NM_020236.4; NP_064621.3.
DR   UCSC; uc003hku.3; human.
DR   AGR; HGNC:14275; -.
DR   CTD; 65008; -.
DR   GeneCards; MRPL1; -.
DR   HGNC; HGNC:14275; MRPL1.
DR   HPA; ENSG00000169288; Low tissue specificity.
DR   MIM; 611821; gene.
DR   neXtProt; NX_Q9BYD6; -.
DR   OpenTargets; ENSG00000169288; -.
DR   PharmGKB; PA30938; -.
DR   VEuPathDB; HostDB:ENSG00000169288; -.
DR   eggNOG; KOG1569; Eukaryota.
DR   GeneTree; ENSGT00940000162168; -.
DR   HOGENOM; CLU_074129_0_0_1; -.
DR   InParanoid; Q9BYD6; -.
DR   OMA; FKHNEKR; -.
DR   OrthoDB; 5353955at2759; -.
DR   PhylomeDB; Q9BYD6; -.
DR   TreeFam; TF314989; -.
DR   PathwayCommons; Q9BYD6; -.
DR   Reactome; R-HSA-5368286; Mitochondrial translation initiation.
DR   Reactome; R-HSA-5389840; Mitochondrial translation elongation.
DR   Reactome; R-HSA-5419276; Mitochondrial translation termination.
DR   SignaLink; Q9BYD6; -.
DR   SIGNOR; Q9BYD6; -.
DR   BioGRID-ORCS; 65008; 130 hits in 1160 CRISPR screens.
DR   ChiTaRS; MRPL1; human.
DR   GeneWiki; MRPL1; -.
DR   GenomeRNAi; 65008; -.
DR   Pharos; Q9BYD6; Tbio.
DR   PRO; PR:Q9BYD6; -.
DR   Proteomes; UP000005640; Chromosome 4.
DR   RNAct; Q9BYD6; Protein.
DR   Bgee; ENSG00000169288; Expressed in left ventricle myocardium and 181 other cell types or tissues.
DR   ExpressionAtlas; Q9BYD6; baseline and differential.
DR   Genevisible; Q9BYD6; HS.
DR   GO; GO:0005743; C:mitochondrial inner membrane; TAS:Reactome.
DR   GO; GO:0005762; C:mitochondrial large ribosomal subunit; NAS:ComplexPortal.
DR   GO; GO:0003723; F:RNA binding; HDA:UniProtKB.
DR   GO; GO:0003735; F:structural constituent of ribosome; IEA:InterPro.
DR   GO; GO:0032543; P:mitochondrial translation; NAS:ComplexPortal.
DR   Gene3D; 3.30.190.20; -; 1.
DR   Gene3D; 3.40.50.790; -; 1.
DR   InterPro; IPR023674; Ribosomal_uL1-like.
DR   InterPro; IPR028364; Ribosomal_uL1/biogenesis.
DR   InterPro; IPR016095; Ribosomal_uL1_3-a/b-sand.
DR   InterPro; IPR005879; Ribosomal_uL1_mit.
DR   NCBIfam; TIGR01170; rplA_mito; 1.
DR   PANTHER; PTHR36427:SF3; 39S RIBOSOMAL PROTEIN L1, MITOCHONDRIAL; 1.
DR   PANTHER; PTHR36427; 54S RIBOSOMAL PROTEIN L1, MITOCHONDRIAL; 1.
DR   Pfam; PF00687; Ribosomal_L1; 1.
DR   SUPFAM; SSF56808; Ribosomal protein L1; 1.
PE   1: Evidence at protein level;
KW   3D-structure; Mitochondrion; Reference proteome; Ribonucleoprotein;
KW   Ribosomal protein; Transit peptide.
FT   TRANSIT         1..50
FT                   /note="Mitochondrion"
FT                   /evidence="ECO:0000255"
FT   CHAIN           51..325
FT                   /note="Large ribosomal subunit protein uL1m"
FT                   /id="PRO_0000252440"
FT   VARIANT         47
FT                   /note="T -> K (in dbSNP:rs17851275)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_027865"
FT   VARIANT         177
FT                   /note="F -> S (in dbSNP:rs17855456)"
FT                   /evidence="ECO:0000269|PubMed:15489334"
FT                   /id="VAR_027866"
FT   CONFLICT        85
FT                   /note="D -> N (in Ref. 7; BAB15005)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        229
FT                   /note="D -> H (in Ref. 4; CAG33472)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        265
FT                   /note="D -> G (in Ref. 7; BAB15005)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   325 AA;  36909 MW;  EB53BEE59065B682 CRC64;
     MAAAVRCMGR ALIHHQRHSL SKMVYQTSLC SCSVNIRVPN RHFAAATKSA KKTKKGAKEK
     TPDEKKDEIE KIKAYPYMEG EPEDDVYLKR LYPRQIYEVE KAVHLLKKFQ ILDFTSPKQS
     VYLDLTLDMA LGKKKNVEPF TSVLSLPYPF ASEINKVAVF TENASEVKIA EENGAAFAGG
     TSLIQKIWDD EIVADFYVAV PEIMPELNRL RKKLNKKYPK LSRNSIGRDI PKMLELFKNG
     HEIKVDEERE NFLQTKIATL DMSSDQIAAN LQAVINEVCR HRPLNLGPFV VRAFLRSSTS
     EGLLLKIDPL LPKEVKNEES EKEDA
//
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