Complement receptor type 2 (CR2)

Homo sapiens — UniProt P20023

Gene: CR2Homo sapiensSwissProt reviewed

About Complement receptor type 2

Complement receptor type 2 (CR2) is a protein from Homo sapiens identified by UniProt accession P20023, 1033 residues long. MolForge cross-references it against 0 known binders and 455 disease associations.

Target properties

Protein nameComplement receptor type 2
UniProt accessionP20023
GeneCR2
OrganismHomo sapiens
Length1033 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (455)

Diseases linked to this target (Open Targets).

  • immunodeficiency, common variable, 7 · score 0.75
  • systemic lupus erythematosus · score 0.46
  • common variable immunodeficiency · score 0.40
  • recurrent infections associated with rare immunoglobulin isotypes deficiency · score 0.39
  • lupus erythematosus · score 0.37
  • Recurrent infections · score 0.37
  • immunodeficiency, common variable, 2 · score 0.34
  • genetic disorder · score 0.19
  • pancreatic adenocarcinoma · score 0.18
  • monocyte count · score 0.14

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-P20023-F1alphafoldPREDICTED74.92—

Amino-acid sequence (1033 residues)

MGAAGLLGVF LALVAPGVLG ISCGSPPPIL NGRISYYSTP IAVGTVIRYS CSGTFRLIGE KSLLCITKDK VDGTWDKPAP KCEYFNKYSS CPEPIVPGGY KIRGSTPYRH GDSVTFACKT NFSMNGNKSV WCQANNMWGP TRLPTCVSVF PLECPALPMI HNGHHTSENV GSIAPGLSVT YSCESGYLLV GEKIINCLSS GKWSAVPPTC EEARCKSLGR FPNGKVKEPP ILRVGVTANF FCDEGYRLQG PPSSRCVIAG QGVAWTKMPV CEEIFCPSPP PILNGRHIGN SLANVSYGSI VTYTCDPDPE EGVNFILIGE STLRCTVDSQ KTGTWSGPAP RCELSTSAVQ CPHPQILRGR MVSGQKDRYT YNDTVIFACM FGFTLKGSKQ IRCNAQGTWE PSAPVCEKEC QAPPNILNGQ KEDRHMVRFD PGTSIKYSCN PGYVLVGEES IQCTSEGVWT PPVPQCKVAA CEATGRQLLT KPQHQFVRPD VNSSCGEGYK LSGSVYQECQ GTIPWFMEIR LCKEITCPPP PVIYNGAHTG SSLEDFPYGT TVTYTCNPGP ERGVEFSLIG ESTIRCTSND QERGTWSGPA PLCKLSLLAV QCSHVHIANG YKISGKEAPY FYNDTVTFKC YSGFTLKGSS QIRCKADNTW DPEIPVCEKE TCQHVRQSLQ ELPAGSRVEL VNTSCQDGYQ LTGHAYQMCQ DAENGIWFKK IPLCKVIHCH PPPVIVNGKH TGMMAENFLY GNEVSYECDQ GFYLLGEKKL QCRSDSKGHG SWSGPSPQCL RSPPVTRCPN PEVKHGYKLN KTHSAYSHND IVYVDCNPGF IMNGSRVIRC HTDNTWVPGV PTCIKKAFIG CPPPPKTPNG NHTGGNIARF SPGMSILYSC DQGYLLVGEA LLLCTHEGTW SQPAPHCKEV NCSSPADMDG IQKGLEPRKM YQYGAVVTLE CEDGYMLEGS PQSQCQSDHQ WNPPLAVCRS RSLAPVLCGI AAGLILLTFL IVITLYVISK HRARNYYTDT SQKEAFHLEA REVYSVDPYN PAS

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Quick facts

UniProtP20023
GeneCR2
OrganismHomo sapiens
Length1033
Binders0
Diseases455
View on UniProt