CPLM 1.0 - Compendium of Protein Lysine Modification
TagContent
CPLM ID CPLM-023273
UniProt Accession
Genbank Protein ID
Genbank Nucleotide ID
Protein Name
 B9 domain-containing protein 1 
Protein Synonyms/Alias
 MKS1-related protein 1 
Gene Name
 B9D1 
Gene Synonyms/Alias
 MKSR1 
Created Date
 July 27, 2013 
Organism
 Homo sapiens (Human) 
NCBI Taxa ID
 9606 
Lysine Modification
Position
Peptide
Type
References
129FVPESTSKLQKFTSWubiquitination[1]
132ESTSKLQKFTSWFMGubiquitination[2, 3, 4]
180VVTKDMRKLGYDTGPubiquitination[2, 4]
Reference
 [1] 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]
 [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] 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]
 [4] 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
Functional Description
 Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Required for ciliogenesis and sonic hedgehog/SHH signaling (By similarity). 
Sequence Annotation
 DOMAIN 9 127 B9.  
Keyword
 Alternative splicing; Cell projection; Ciliopathy; Cilium biogenesis/degradation; Complete proteome; Cytoplasm; Cytoskeleton; Meckel syndrome; Polymorphism; Reference proteome. 
Sequence Source
 UniProt (SWISSPROT/TrEMBL); GenBank; EMBL 
Protein Length
 204 AA 
Protein Sequence
MATASPSVFL LMVNGQVESA QFPEYDDLYC KYCFVYGQDW APTAGLEEGI SQITSKSQDV 60
RQALVWNFPI DVTFKSTNPY GWPQIVLSVY GPDVFGNDVV RGYGAVHVPF SPGRHKRTIP 120
MFVPESTSKL QKFTSWFMGR RPEYTDPKVV AQGEGREVTR VRSQGFVTLL FNVVTKDMRK 180
LGYDTGPSDT QGVLGPSPPQ SFPQ 204 
Gene Ontology
 GO:0005813; C:centrosome; IDA:UniProtKB.
 GO:0035085; C:cilium axoneme; IEA:UniProtKB-SubCell.
 GO:0005932; C:microtubule basal body; IDA:UniProtKB.
 GO:0036038; C:TCTN-B9D complex; ISS:UniProtKB.
 GO:0008158; F:hedgehog receptor activity; ISS:UniProtKB.
 GO:0042384; P:cilium assembly; ISS:UniProtKB.
 GO:0007224; P:smoothened signaling pathway; ISS:UniProtKB. 
Interpro
 IPR010796; B9_dom. 
Pfam
 PF07162; B9-C2 
SMART
  
PROSITE
 PS51381; B9 
PRINTS