P15529

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession MCP_HUMAN; P15529;
Entrez ID 4179
GenBank Protein ID NM_002389.4; NM_153826.3; NM_172350.2; NM_172351.2; NM_172352.2; NM_172353.2; NM_172359.2; NM_172361.2; XM_011509563.1; XM_011509564.1; XM_017001308.1; XM_017001309.1; XM_017001310.1;
GenBank Nucleotide ID NP_002380.3; NP_722548.1; NP_758860.1; NP_758861.1; NP_758862.1; NP_758863.1; NP_758869.1; NP_758871.1; XP_011507865.1; XP_011507866.1; XP_016856797.1; XP_016856798.1; XP_016856799.1;
Protein Name Membrane cofactor protein (TLX) (Trophoblast leukocyte common antigen) (CD antigen CD46)
Gene Name CD46; MCP; MIC10
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionActs as a cofactor for complement factor I, a serine protease which protects autologous cells against complement-mediated injury by cleaving C3b and C4b deposited on host tissue. May be involved in the fusion of the spermatozoa with the oocyte during fertilization. Also acts as a costimulatory factor for T-cells which induces the differentiation of CD4+ into T-regulatory 1 cells. T-regulatory 1 cells suppress immune responses by secreting interleukin-10, and therefore are thought to prevent autoimmunity.;(Microbial infection) A number of viral (view all)
Sequence
(Fasta)
MEPPGRRECP FPSWRFPGLL LAAMVLLLYS FSDACEEPPT FEAMELIGKP KPYYEIGERV 60
DYKCKKGYFY IPPLATHTIC DRNHTWLPVS DDACYRETCP YIRDPLNGQA VPANGTYEFG 120
YQMHFICNEG YYLIGEEILY CELKGSVAIW SGKPPICEKV LCTPPPKIKN GKHTFSEVEV 180
FEYLDAVTYS CDPAPGPDPF SLIGESTIYC GDNSVWSRAA PECKVVKCRF PVVENGKQIS 240
GFGKKFYYKA TVMFECDKGF YLDGSDTIVC DSNSTWDPPV PKCLKVLPPS STKPPALSHS 300
VSTSSTTKSP ASSASGPRPT YKPPVSNYPG YPKPEEGILD SLDVWVIAVI VIAIVVGVAV 360
ICVVPYRYLQ RRKKKGTYLT DETHREVKFT SL 393

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1PhosphorylationLymphomaP8649859
[Reference]: We also found an oncogenic form of cbl protein in the 70Z/3 pre-B cell lymphoma which exhibits deregulated tyrosine phosphorylation.

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 2)
MESH:D065766 ; Atypical Hemolytic Uremic Syndrome
MESH:D008457 ; Measles
DisGeNet (Curated)
(count: 4)
C0025007; Measles
C0162739; HELLP Syndrome
C2752040; HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2
C2931788; Atypical Hemolytic Uremic Syndrome
GWASdb
(count: 4)
rs2724387; Amyotrophic lateral sclerosis (sporadic); amyotrophic lateral sclerosis
rs17006738; IgE levels; selective IgE deficiency disease
rs7545126; Obesity-related traits; obesity
rs11118555; Heart rate; heart conduction disease

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 5)
303       ALSHSVSTSSTTKSP     dbPAF
320       SASGPRPTYKPPVSN     dbPAF
368       ICVVPYRYLQRRKKK     dbPAF
378       RRKKKGTYLTDETHR     dbPAF
391       HREVKFTSL******     dbPAF
Acetylation
(count: 2)
153       SVAIWSGKPPICEKV     PLMD
159       GKPPICEKVLCTPPP     PLMD
Ubiquitination
(count: 5)
224       SRAAPECKVVKCRFP     PLMD
237       FPVVENGKQISGFGK     PLMD
375       YLQRRKKKGTYLTDE     PLMD
388       DETHREVKFTSL***     PLMD
66        RVDYKCKKGYFYIPP     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource