dbacp06134
General Description
Peptide name : Solute carrier family 15 member 2
Source/Organism : Rabbit
Linear/Cyclic : Not found
Chirality : D
Sequence Information
Sequence : MNPFQQNESKETLFSPVSTEETPPRLSSPAKKTPPKICGSNYPLSIAFIVVNEFCERFSYYGMKAVLTLYFLYFLHWNEDTSTSVYHAFSSLCYFTPILGAAIADSWLGKFKTIIYLSLVNVLGHVIKSLSAFPILGGKVVHTVLSLVGLCLIALGTGGIKPCVAAFGGDQFEEKHAEERTRYFSGFYLAINAGSLISTFITPMLRGDVQCFGEDCYALAFGVPGLLMVIALVVFAMGSKMYKKPPPEGNIVAQVVKCIWFAISNRFKNRSEDIPKRQHWLDWAAEKYPKQLIMDVKTLTRVLFLYIPLPMFWALLDQQGSRWTLQATKMNGNLGFFVLQPDQMQVLNPLLVLIFIPLFDLVIYRLISKCGINFTSLRKMAVGMVLACLAFAAAATVEIKINEMAPPQPGSQEILLQVLNLADDEVKLTVLGNNNNSLLADSIKSFQKTPHYSKIHLNTKSQDFYFHLKYHNLSIYTEHSVEERNWYSLIIREDGKSISSIMVKDMENETTYGMTAIRFINTLQENVNISLGTDISLNVGENYGVSAYRTVQRGEYPAVHCKTEDKDFSLNLGLLDFGASYLFVITNSTKQGLQAWKMEDIPANKVSIAWQLPQYALVTAGEVMFSVTGLEFSYSQAPSSMKSVLQAAWLLTVAIGNIIVLVVAQFSGLVQWAEFVLFSCLLLVVCLIFSIMGYYYIPIKSEDIQGPEDKQIPHMQGnMINLETKKTKL
Peptide length: 729
C-terminal modification: Not found
N-terminal modification : Not found
Non-natural peptide information: None
Activity Information
Assay type : Not specified
Assay time : Not found
Activity : Not found
Cell line : Not found
Cancer type : Not found
Other activity : Not found
Physicochemical Properties
Amino acid composition bar chart :
Molecular mass : 81663.2299 Dalton
Aliphatic index : 1.015
Instability index : 34.5561
Hydrophobicity (GRAVY) : 0.1995
Isoelectric point : 7.164
Charge (pH 7) : 0.5599
Aromaticity : 0.115
Molar extinction coefficient (cysteine, cystine): (110700, 111450)
Hydrophobic/hydrophilic ratio : 1.26791277
hydrophobic moment : -0.009
Missing amino acid : None
Most occurring amino acid : L
Most occurring amino acid frequency : 84
Least occurring amino acid : n
Least occurring amino acid frequency : 1
Structural Information
3D structure : Not Available
Secondary structure fraction (Helix, Turn, Sheet): (0.3, 0.2, 0.4)
SMILES Notation: 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Secondary Structure :
| Method | Prediction |
|---|---|
| GOR | CCCHHHTTTTHEEECTTCCTTCCCTTCCTTTCCCCEEETCCCCCEEEEEEHHTHHHHHHHTTCHTHHHHHEEEEEETTTTTTEEEEEETTTTTECCCCECCHHHHHHHTTTEEEEEEEEEEEEEEEEEEETCCHEETTEEEEEEEEEEEEEEEEECCCCCCCEEEHTTCHHHHHHHHHHHHHHTTTEEEEECTTCEEEEEECCCCTTCCTTTTTTHHHHTTCCCTCEEEHHHHHHHHHHHHTTCCCCTTCEEEEEHHEEHHHHHHHHTTTTTHCHHHHHHHHHHHHHCHHHHEHHHHHHHHEEEEECCCCHHHHHHHHTTCHHEHHHHHTTTCCEEEEECCCCHEECCTTEEEEECCCHHHHEEEEEETTCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCEEEEEEHHHHHHHHEEEEETCCTTCEEHHHHHETTTCCTTEEEEETTTTTHHHEHHTTTTTTEEEETHHHHHHHHHHHHHHTTCCHHEEEHHHHTTHHHTTCEEEEEHHCHTTTCEEEEEEEEEEEETCEEEEEEEEEEETTCCTHHHHHCTTHHHHTTTTEEETTCEEEEEEECCCCHHHHHHHHHHCHHHHHEEEEHCHTHHEEEHHHEEEEETCCEEEETCCCTTEEEHHHHHHHEEEEEEEEEEEEEEEEHTHHHHHHHHHHHHHTHHEEEEEEEECCECCCCCCCCCTCCHTHHCHHHTTCHHHHHHHHHHH |
| Chou-Fasman (CF) | CCCHHHHHHHHCCEEEECCCCCCCCCCCCCCCCCCEECCCCEEEEEEEEEHHHHHHEEEECCCCEEEEEEEEEHHHHHHEEEEEECCCEEEEEEEEEEHHHHHHHCHHHHEEEEEEEEEEEEEEEEECCCCEEEECEEEEEEEEEEEEEECCEEECEECCEECCCCCCCHHHHHHHHHHEEEEEEECCCCCCCEEEEEEEEECCCEEEEEHHHHHHHHHEEEECCEEEEEEEECCCCCCCCCCCCCCCEEEEEEEEEEEEECCCCCCCCCCCCCCHHHHHHHHHHCCCHHHHCCEEEEEEEEEEEECCCCHHHHHHCCCCEEEHHHHHCCCCCEEEEECCCCEEEECCEEEEEEEECCEEEEEEEEECEEEEEEEHHHHHHEECCHHHHHHHHHHCCCCHHHHCCCCCCCCCCEEEEEHHHHHHHEEEEECCCCCHHHHHCEECCCCCCCCCCCCCCCCCCEEEECCCCCCEEEEHHHHHHHHEEEEEEECCCCEEEEEEEHHHHHHCEEEECEEEEEEEECCCCEEEEEEEEEEEECCCCEEEECEEEEECCCCCHHHHHHHHHHHCHHHHHHHHCCEEEEEEEECCCHHHHHHHHHHCCCCCEEEECCCCCCEEEEHHHHEEEEEHHHHEEECCCCCCEEEHHHHHEEEEECEEEEEEEEECEEEEEEHHHHEEEEECEEEEEEEEEEEEEEEEECHHHHEECCCCCCEECCCCCCCHHHHCCCCCC |
| Neural Network (NN) | CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCEEEEEEHHHHHHHHHCCHHHHHHHHHHHHHCCCCCCCCEEEEEECCCCCCCCCCCCHHHHHHHHCCCEEEEEEEHHHHHHHHCCCCCCCCCCCCEEEEEEHHHHHEEEECCCCCCCCCECCCCCCCHHHHHHHHHHHHCCCCEEEECCCCCEEEECCCCCCCCCCCCCCCCCHHCCCCCCHHHHHHHHHHHHHCCCCCCCCCCCCCHHHHHHHHEHHHCCCCCCCCCCCCCCHHHHHHHHCCCCCCHHHHHHHHHHHHEHCCCCCCHHHHHHCCCCCHHHHHHHCCCCCCCCCCCCCCHHHHCCHHHHHHCCCCHHHHHEEECCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCCCHHHHHHHCCCHHHHHHHHHCCCCCCCHHHCCCCCCCCCCCCEEECCCCCCHHHHHHHCCCCCEECCCCCHHHCCCEEEEECCCCCCCCEEEECCCCCCCCCCEEEEEECCCCCCCCECCCCCCEEECCCCCCCEEEEEECCCCCCCECCCCCCCCHHHHHHHHHCCCCEEEEEECCCCCCCHHHCCCCCCCCCCCHHHCCCCHHHHHHCCEEEEEECCCCCCCCCCCCCHHHHHHHHHHHHHCCCEEEEEEHHHCHHHHHHHHHHHHHHHHHHHHEEECCCCEECCCCCCCCCCCCCCCCCCCCCCHHHHHHHCCCC |
| Joint/Consensus | CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCEECCCCCCCEEEEEEHHHHHHHHHHCCCCCHHHHHEEECCCCCCCCCEEEEEEECCCCCCCCCCCCHHHHHHHHCCEEEEEEEEEEEEEEEECCCCCCCCCCCEEEEEEEEEEEEEEEEECCCCCCCCCCCCCCHHHHHHHHHHHHHHCCCCEEEECCCCEEEEEECCCCCCCCCCCCCCHHHHCCCCCCCEEEHHHHHHHHHCCCCCCCCCCCCEEEEECCEEECCCCCCCCCCCCCCCHHHHHHHHHHCCCHHHHCHHHHHHHHEEEEECCCCHHHHHHHCCCCCHHHHHHHCCCCCEEEECCCCCCEECCCCEEEEECCCCCCCEEEEECCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCCEEEEEHHHHHHHHEEEECCCCCCCCCCCCCCCCCCCCCCCEEECCCCCCCCCCCCCCCCCCEECCCHHHHHCCCEEECCCCCCCCCEEEHHHHCCCCCCCCEEEEEECCCCCCCEEEEEEEEEEECCCEEEEEEEEEECCCCCCHHHHHCCCHHHHHHHHHHHCCCEEEEEEECCCCHHHHHHHHHCCCCCCCEECCCCCCCCEEHHHHEEEEECCCCEEECCCCCCEEEHHHHHHHEEEEEEEEEEEEEEEECCHHHHHHHHHHHHHCCCEEEEEEEECCEECCCCCCCCCCCCCCCCCCCCCCHHHHHHHCCCC |
Molecular Descriptors and ADMET Properties
Molecular Descriptors: Not available.
ADMET Properties: Not available.
Cross Referencing databases
CancerPPD : Not available
ApIAPDB : Not available
CancerPPD2 ID : Not available
Reference
1 : Boll M, et al. Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter. Proc Natl Acad Sci U S A. 1996; 93:284-9. doi: 10.1073/pnas.93.1.284
Literature
Paper title : Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter.
Doi : https://doi.org/10.1073/pnas.93.1.284
Abstract : The presence of a proton-coupled electrogenic high-affinity peptide transporter in the apical membrane of tubular cells has been demonstrated by microperfusion studies and by use of brush border membrane vesicles. The transporter mediates tubular uptake of filtered di- and tripeptides and aminocephalosporin antibiotics. We have used expression cloning in Xenopus laevis oocytes for identification and characterization of the renal high-affinity peptide transporter. Injection of poly(A)+ RNA isolated from rabbit kidney cortex into oocytes resulted in expression of a pH-dependent transport activity for the aminocephalosporin antibiotic cefadroxil. After size fractionation of poly(A)+ RNA the transport activity was identified in the 3.0- to 5.0-kb fractions, which were used for construction of a cDNA library. The library was screened for expression of cefadroxil transport after injection of complementary RNA synthesized in vitro from different pools of clones. A single clone (rPepT2) was isolated that stimulated cefadroxil uptake into oocytes approximately 70-fold at a pH of 6.0. Kinetic analysis of cefadroxil uptake expressed by the transporter's complementary RNA showed a single saturable high-affinity transport system shared by dipeptides, tripeptides, and selected amino-beta-lactam antibiotics. Electrophysiological studies established that the transport activity is electrogenic and affected by membrane potential. Sequencing of the cDNA predicts a protein of 729 amino acids with 12 membrane-spanning domains. Although there is a significant amino acid sequence identity (47%) to the recently cloned peptide transporters from rabbit and human small intestine, the renal transporter shows distinct structural and functional differences.