Ribosomal protein L10

Function

Ribosomal protein L10 (RPL10) is one of the 34 proteins which belong to the of the prokaryotic ribosome or to the ca. 49 proteins in the large 60S subunit of the eukaryotic ribosome[1]. It is found mostly in eubacteria. The L10 forms a complex with a dimer of L7/L12. This complex is called L8. The acidic ribosomal protein P0 is the equivalent of the 50S L10 and the 60S L10E.

Relevance

Mutation in RPL10 causes X-linked intellectual disability and cerebellar hypoplasia[2].

Human ribosomal protein L10 core domain complex with K+ ion (PDB code 2pa2)

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3D Structures of Ribosomal protein L103D Structures of Ribosomal protein L10

Updated on 27-February-2022

2pa2 – RPL10 core domain – human
1zav, 1zaw, 1zax – RPL10+RPL7 N-terminal – Thermotoga maritima
3a1y - RPL10 N-terminal+RPL12 – Pyrococcus horikoshii
3jsy – MjRPL10 N-terminal – Methanocaldocoddus jannaschii
5d6g – MjRPL10 + 23S RNA
5dar – MjRPL10 + RPL11 + 23S RNA
5d8h – MjRPL10 + RPL11 + 23S RNA + thiostrepton

ReferencesReferences

  1. Falcone Ferreyra ML, Casadevall R, Luciani MD, Pezza A, Casati P. New evidence for differential roles of l10 ribosomal proteins from Arabidopsis. Plant Physiol. 2013 Sep;163(1):378-91. doi: 10.1104/pp.113.223222. Epub 2013 Jul , 25. PMID:23886624 doi:http://dx.doi.org/10.1104/pp.113.223222
  2. Zanni G, Kalscheuer VM, Friedrich A, Barresi S, Alfieri P, Di Capua M, Haas SA, Piccini G, Karl T, Klauck SM, Bellacchio E, Emma F, Cappa M, Bertini E, Breitenbach-Koller L. A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia. Hum Mutat. 2015 Dec;36(12):1155-8. doi: 10.1002/humu.22860. Epub 2015 Sep 14. PMID:26290468 doi:http://dx.doi.org/10.1002/humu.22860

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