ADAN database


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Protein (*) Link 1 Link 2 Peptide Position Foldx Score Mint Code (*) Interactions Mint Score PubMed Short Description (*)
Q5KSL6 APID UniProt PSPSPSPSPRT 197-207 4.65 nd nd nd nd DGKK_HUMAN Diacylglycerol kinase kappa - Homo sapiens
Q1HE16 APID UniProt APGHPLAKGYL 13-23 4.65 nd nd nd nd Q1HE16_HUMAN Feline leukemia virus subgroup C cellular receptor - Homo sapiens
Q16144 APID UniProt SLCRPGAPLLN 20-30 4.65 nd nd nd nd Q16144_HUMAN Cholecystokinin B receptor - Homo sapiens
Q6F5E8 APID UniProt PSCRPGPGSQG 1273-1283 4.65 nd nd nd nd LR16C_HUMAN Leucine-rich repeat-containing protein 16C - Homo sapiens
Q68DL5 APID UniProt DGPHAPVPCLL 220-230 4.65 nd nd nd nd Q68DL5_HUMAN Putative uncharacterized protein DKFZp686M13211 - Homo sapiens
Q5THL0 APID UniProt RGGFPPRGPRG 494-504 4.65 nd nd nd nd Q5THL0_HUMAN Ewing sarcoma breakpoint region 1 - Homo sapiens
Q6IB64 APID UniProt PSRKRPELPRA 109-119 4.65 nd nd nd nd Q6IB64_HUMAN TCEA2 protein - Homo sapiens
Q9Y5Y0 APID UniProt APGHPLAKGYL 13-23 4.65 nd nd nd nd FLVC1_HUMAN Feline leukemia virus subgroup C receptor-related protein 1 - Homo sapiens
P59051 APID UniProt APAVPRRGPRS 130-140 4.65 nd nd nd nd CU087_HUMAN Uncharacterized protein C21orf87 - Homo sapiens
Q8TDC3 APID UniProt GEQPPPPSARS 505-515 4.65 nd nd nd nd BRSK1_HUMAN BR serine/threonine-protein kinase 1 - Homo sapiens
Q5TAV2 APID UniProt FKPLPRPPPLA 228-238 4.65 nd nd nd nd Q5TAV2_HUMAN Deafness, autosomal recessive 31 - Homo sapiens
Q5TG53 APID UniProt AGPGPRAPARS 12-22 4.65 nd nd nd nd Q5TG53_HUMAN Chromosome 1 open reading frame 133 - Homo sapiens
Q9P1D2 APID UniProt SSCTAPPRPRS 9-19 4.65 nd nd nd nd Q9P1D2_HUMAN PRO2472 - Homo sapiens
Q5T0W9 APID UniProt YKPHFVPNFNG 358-368 4.65 nd nd nd nd FA83B_HUMAN Protein FAM83B - Homo sapiens
Q9Y4F5 APID UniProt SRGRRSPRAPG 780-790 4.65 nd nd nd nd K0284_HUMAN Protein KIAA0284 - Homo sapiens
O95137 APID UniProt HPSELPIPQRL 275-285 4.65 nd nd nd nd O95137_HUMAN Cell cycle related kinase - Homo sapiens
Q5TAV1 APID UniProt FKPLPRPPPLA 196-206 4.65 nd nd nd nd Q5TAV1_HUMAN Deafness, autosomal recessive 31 - Homo sapiens
Q86V09 APID UniProt PPPAPRPTSRY 492-502 4.65 nd nd nd nd Q86V09_HUMAN Fragile X mental retardation, autosomal homolog 2 - Homo sapiens
A8K7P9 APID UniProt SLCRPGAPLLN 20-30 4.65 nd nd nd nd A8K7P9_HUMAN cDNA FLJ77169, highly similar to Homo sapiens cholecystokinin B receptor (CCKBR), mRNA - Homo sapiens
Q9H1U4 APID UniProt EPSHPFPRATA 62-72 4.65 nd nd nd nd MEGF9_HUMAN Multiple epidermal growth factor-like domains 9 precursor - Homo sapiens

 


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