2ZN9,1Y1X


Conserved Protein Domain Family
EFh_PEF_Group_I

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cd16180: EFh_PEF_Group_I 
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Penta-EF hand, calcium binding motifs, found in Group I PEF proteins
The family corresponds to Group I PEF proteins that have been found not only in higher animals but also in lower animals, plants, fungi and protists. Group I PEF proteins include apoptosis-linked gene 2 protein (ALG-2), peflin and similar proteins. ALG-2, also termed programmed cell death protein 6 (PDCD6), is a widely expressed calcium-binding modulator protein associated with cell proliferation and death, as well as cell survival. It forms a homodimer in the cell or a heterodimer with its closest paralog peflin. Among the PEF proteins, ALG-2 can bind three Ca2+ ions through its EF1, EF3, and EF5 hands, where it is unique in that its EF5 hand binds Ca2+ ion in a canonical coordination. Peflin is a ubiquitously expressed 30-kD PEF protein containing five EF-hand motifs in its C-terminal domain and a longer N-terminal hydrophobic domain (NHB domain) than any other member of the PEF family. The NHB domain harbors nine repeats of a nonapeptide (A/PPGGPYGGP). Peflin may modulate the function of ALG-2 in Ca2+ signaling. It exists only as a heterodimer with ALG-2, and binds two Ca2+ ions through its EF1 and EF3 hands. Its additional EF5 hand is unpaired and does not bind Ca2+ ion but mediates the heterodimerization with ALG-2. The dissociation of heterodimer occurs in the presence of Ca2+.
Statistics
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PSSM-Id: 320055
Aligned: 40 rows
Threshold Bit Score: 183.113
Created: 18-Nov-2014
Updated: 2-Oct-2020
Structure
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Program:
Drawing:
Aligned Rows:
  next features
Conserved site includes 11 residues -Click on image for an interactive view with Cn3D
Feature 1:Ca binding site [ion binding site]
Evidence:
  • Comment:Due to the presence of unfavorable residues at the Ca2+-coordinating positions, the EF5 hand of some family members may not be able to bind Ca2+ ion.
  • Structure:2ZN9; Homo sapiens ALG-2 binds three Ca2+ ions through its EF1, EF3 and EF5 hands.
    View structure with Cn3D
  • Structure:1Y1X; Leishmania major Friedlin PDCD6-like protein binds two Ca2+ ions through its EF1 and EF2 hands.
    View structure with Cn3D

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                 # # #      #                                                           
2ZN9_A         8 FLWNVFQRVDKDRSGVISDTELQQALSNGTwtpf--npvTVRSIISMF--DRENKAGVNFSEFTGVWKYITDWQNVFRTY 83  human
1Y1X_A        28 ELMEWFRAVDTDGSGAISVPELNAALSSAGvpf---slaTTEKLLHMY--DKNHSGEITFDEFKDLHHFILSMREGFRKR 102 Leishmania majo...
CEF63908      11 AADAFFLILDRNRSGTISMDEFQRGMSNGTterf--dmdTVSLLFAMI--DREGHKKLNMSQFRVVFSFVEAWKRAFHAV 86  Strongyloides r...
Q8W4L0       168 NIVACFQAADRDNSGFIDDKELQGALSSYNqsf---sirTVHLLMYLF--TNSNVRKIGPKEFTSLFFSLQNWRSIFERF 242 thale cress
CDP06909     125 GVIRTFQMVDRDGSGFIEESELRQALSSGYqrf---smrTIRLLIFLFknPSDSALRIGPKEFSALWSCLGQWRAIFERF 201 Coffea canephora
Q9ZQH1        56 EIVRSFESADRNRSGFLEESELRQALSLSGydgi--snrTIRLLLFIYkiPVDSLLRLGPKEYVELWNCLAQWRAIFNRY 133 thale cress
ABR17289      87 EIIRSFQMCDQDGSGFIDDKELQRALSSAShsf---slrTVHLLMFEF--TRNNSMKIGPQEFTSLWHSLQAWRAIFERF 161 Sitka spruce
XP_001757697   8 EVTRLFQMADLDRSGTIDAHELGRVLSTGRvaf---sprTLRLMLHLFgdLKNDSTRIGPVGFAKLWKEIQQWNKKFSEF 84  Physcomitrella ...
XP_002119334  11 RLWAKFQACDKDKNGSITVDELRASLLSGCdyqrpfsyeVCRMMMSMY--DKNRNGRLTFDEYVNLDGYIRNWYGYFTRN 88  vase tunicate
XP_003737924  28 KIEELFRMMDVAGRGRLDKPELVEGMKYYNgisl--kteTIVLLAGMY--GSEATGGLTLEDFKRLHHTLMTWSSLFRRH 103 western predato...
Feature 1        # # #      #                                                        # # #       
2ZN9_A        84 DrDNSGMIDKNELKQALSGFGyrlsdqFHDILIRKFDRq--GRGQIAFDDFIQGCIVLQRLTDIFRRYDtDQDGWIQVSY 161 human
1Y1X_A       103 DsSGDGRLDSNEVRAALLSSGyqvseqTFQALMRKFDRq--RRGSLGFDDYVELSIFVCRVRNVFAFYDrERTGQVTFTF 180 Leishmania majo...
CEF63908      87 DrDRSGAIEVREFKELLYHMGykisdaSIMLFVNKFARk--RPMTLFFDDFIRSVISLQLLTDAFKVKDiGKQGFIQLSY 164 Strongyloides r...
Q8W4L0       243 DkDRSGRIDTNELRDALMSLGfsvspvILDLLVSKFDKsggRNRAIEYDNFIECCLTVKGLTEKFKEKDtALSGSAIFNY 322 thale cress
CDP06909     202 DrDRSGKIDATELRDALNGIGytvppsVFQVLISRYEEgngRRVELSFDSFVECGMIVKGLTEKFKEKDpRYTGSATMTY 281 Coffea canephora
Q9ZQH1       134 DrDRSGKMNSTQLRDAFYNLGcvlptsVHQLIVSQFDDgtgKTVDLCFDSFLECGMIVKGLTEKFRENDpGYTGYATLSY 213 thale cress
ABR17289     162 DrDRSGKIETMELRDALLSLGysisptILQTLVSKYDKt-gQSRGIDYDNFIECSLVVKGLTDKFKEKDkSYVGSASLTY 240 Sitka spruce
XP_001757697  85 DrDGSGSIDAQELHQALMSFNfnippsVLQMLVSKYDVt-gGSRSIGYDNFVECGFVVKGLTEKFKGQDkSLTGNATFDY 163 Physcomitrella ...
XP_002119334  89 DvNRDGRLEHRDFQTAITGLGfrlnqdFFNQIWMDLMKg-aGSNGVVFDQFMHVCIVMQMLTNAWNKRVpNNVTTLEIEH 167 vase tunicate
XP_003737924 104 DvDSQEYLLHHSLCSALHELGykldrtTTRSLTRKLGR---QAKYIQEDAFVRICCLLRRLSTAFKKKDlNRQKNIQLSY 180 western predato...
Feature 1                  
2ZN9_A       162 EQYLSMVFSI 171 human
1Y1X_A       181 DTFIGGSVSI 190 Leishmania major strain Friedlin
CEF63908     165 EEFLLILGQS 174 Strongyloides ratti
Q8W4L0       323 ENFMLTVLPF 332 thale cress
CDP06909     282 DSFMSMIIPF 291 Coffea canephora
Q9ZQH1       214 DVFMLMVIPF 223 thale cress
ABR17289     241 EEFMQIVLPF 250 Sitka spruce
XP_001757697 164 TSFMLMVIPF 173 Physcomitrella patens
XP_002119334 168 VDFASIIMGI 177 vase tunicate
XP_003737924 181 YEVLHMALDS 190 western predatory mite

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