Protein information for: OR1E2
MMGQNQTSISDFLLLGLPIQPEQQNLCYALFLAMYLTTLLGNLLIIVLIR
LDSHLHTPVYLFLSNLSFSDLCFSSVTMPKLLQNMQNQDPSIPYADCLTQ
MYFFLYFSDLESFLLVAMAYDRYVAICFPMHYTAICAIMSPMLCLSVVAL
SWVLTTFHAMLHTLLMARLCFCADNVIPHFFCDMSALLKLACSDTRVNEW
VIFIMGGLILVIPFLLILGSYARIVSSILKVPSSKGICKAFSTCGSHLSV
VSLFYGTVIGLYLCPSANSSTLKDTVMAMMYTVVTPMLTPFIYSLRNRDM
KGALERVICKRKNPFLL
In red: predicted N-glycosylation site.
In magenta: Conserved cysteines that are predicted to form a disulfide bond.
Underlined and bold: TM regions.
Predicted binding site residues (CDRs) are highlighted according to the following amino acid color code:
| | basic (H,R,K)
| | hydrophilic, no charge (Q,N,T,S)
| | aliphatic (M,A,I,L,V)
| | aromatic (F,Y,W)
| | helix breakers (G,P)
| | acidic (D,E)
| | cysteine (C)
Sequences of the TM regions:
TM | Start position | End position | Sequence |
TM1 | 24 | 50 | QNLCYALFLAMYLTTLLGNLLIIVLIR |
TM2 | 61 | 83 | LFLSNLSFSDLCFSSVTMPKLLQ |
TM3 | 98 | 118 | LTQMYFFLYFSDLESFLLVAM |
TM4 | 144 | 164 | CLSVVALSWVLTTFHAMLHTL |
TM5 | 201 | 222 | VIFIMGGLILVIPFLLILGSYA |
TM6 | 244 | 268 | CGSHLSVVSLFYGTVIGLYLCPSAN |
TM7 | 274 | 293 | DTVMAMMYTVVTPMLTPFIY |
The information was derived from a multiple alignment of ORs, based on the algorithms of Man et al. Protein Sci. 2004 Jan;13(1):240-54.
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