ADAN database


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Records 1341 to 1360 of 10000 		     Records Per Page 
Protein (*) Link 1 Link 2 Peptide Position Foldx Score Mint Code (*) Interactions Mint Score PubMed Short Description (*)
A6NF26 APID UniProt GPLGTPGEQGLIG 1171-1183 6.07 nd nd nd nd A6NF26_HUMAN Uncharacterized protein COL27A1 - Homo sapiens
A6NFR5 APID UniProt GAEGSPGLPGLLG 334-346 6.07 nd nd nd nd A6NFR5_HUMAN Uncharacterized protein COL13A1 - Homo sapiens
Q5TAT6 APID UniProt GAEGSPGLPGLLG 356-368 6.07 nd nd nd nd CODA1_HUMAN Collagen alpha-1(XIII) chain - Homo sapiens
Q19QZ9 APID UniProt SPFLWPGVEGPDS 1877-1889 6.29 nd nd nd nd Q19QZ9_HUMAN T calcium channel alpha 1G subunit variant 217 - Homo sapiens
Q9NUB7 APID UniProt GLPGDPGLPGQPG 678-690 6.29 nd nd nd nd Q9NUB7_HUMAN Collagen type IV alpha 5 - Homo sapiens
Q19QZ5 APID UniProt SPFLWPGVEGPDS 1831-1843 6.29 nd nd nd nd Q19QZ5_HUMAN T calcium channel alpha 1G subunit variant 313 - Homo sapiens
Q9Y566 APID UniProt QPRGRPSSSGTPR 512-524 6.29 nd nd nd nd SHAN1_HUMAN SH3 and multiple ankyrin repeat domains protein 1 - Homo sapiens
Q9P202 APID UniProt LPLGQPRKLGRED 594-606 6.29 nd nd nd nd WHRN_HUMAN Whirlin - Homo sapiens
A7E246 APID UniProt PAHPSLLLHGPSG 354-366 6.29 nd nd nd nd A7E246_HUMAN Integrin, alpha 3 - Homo sapiens
Q19R00 APID UniProt SPFLWPGVEGPDS 1877-1889 6.29 nd nd nd nd Q19R00_HUMAN T calcium channel alpha 1G subunit variant 216 - Homo sapiens
Q19R10 APID UniProt SPFLWPGVEGPDS 1863-1875 6.29 nd nd nd nd Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
Q2TAC4 APID UniProt SPFLWPGVEGPDS 1865-1877 6.29 nd nd nd nd Q2TAC4_HUMAN Calcium channel, voltage-dependent, T type, alpha 1G subunit - Homo sapiens
Q19R04 APID UniProt SPFLWPGVEGPDS 1888-1900 6.29 nd nd nd nd Q19R04_HUMAN T calcium channel alpha 1G subunit variant 184 - Homo sapiens
Q6DN14 APID UniProt SSSPQPPPRGDRA 167-179 6.29 nd nd nd nd MCTP1_HUMAN Multiple C2 and transmembrane domain-containing protein 1 - Homo sapiens
Q8TCX5 APID UniProt MVLPRPPRAGSQP 376-388 6.29 nd nd nd nd RHPN1_HUMAN Rhophilin-1 - Homo sapiens
Q19QZ7 APID UniProt SPFLWPGVEGPDS 1877-1889 6.29 nd nd nd nd Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
Q5TAV1 APID UniProt LPLGQPRKLGRED 211-223 6.29 nd nd nd nd Q5TAV1_HUMAN Deafness, autosomal recessive 31 - Homo sapiens
Q19R12 APID UniProt SPFLWPGVEGPDS 1854-1866 6.29 nd nd nd nd Q19R12_HUMAN T calcium channel alpha 1G subunit variant 89 - Homo sapiens
A4D2H0 APID UniProt IPPPLAPVRGPLF 694-706 6.3 nd nd nd nd A4D2H0_HUMAN Putative uncharacterized protein LOC389592 - Homo sapiens
Q86UF2 APID UniProt IPPPLAPVRGPLF 649-661 6.3 nd nd nd nd CTGE6_HUMAN Protein cTAGE-6 - Homo sapiens

 


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