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 Description | Acts 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 |
|
Database | Annotation |
---|---|
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 | 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 |
Network | Interaction | ||
---|---|---|---|
A | B | Source | |