Q8N1D0 AF NFT

Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein

MOLNFT AF v1 smart contract in GenesisL1 blockchain: 
0xBf7491af3407816DFa88a5EA4c82e8A2B1D721eD
IPFS of NFT metadata: 
bafybeifm3t7jacbxiyrjubd2emj7ige6ijbvcglfsswaslrl2apkswffny/metadata.json
IPFS of structure file: 
bafybeiclfyrchldtbrxfvmrgn2bfliqc3ye425gbdwyf6tjwlmwcyqqn6u/AF-Q8N1D0-F1-model_v2.pdb
First NFT owner address (eip-55): 
0xB44F19a0cb161828322eEEd13F55d4C3C34938d2
First NFT owner address (bech32): 
genesis1k383ngxtzcvzsv3wamgn74w5c0p5jwxjy9e46q
Current NFT ID #47388 owner (web3):

First owner GALLERY | EVM EXPLORER | COSMOS EXPLORER

MOLNFT AF v1

NFT id:
47388
Accession (UniProt):
Q8N1D0
Name::
Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein
Experimental Method:
Predicted structure
Sequence source:
HOMO SAPIENS

NFT data

MolNFT AF v1 is an AlphaFold database of AI predicted Swiss-Prot protein sequences preserved as regular ERC-721 NFT tokens on GenesisL1 blockchain for public free use, research and entertainment:

https://alphafold.ebi.ac.uk/
Jumper, J., Evans, R., Pritzel, A. et al. Highly accurate protein structure prediction with AlphaFold. 
Nature 596, 583–589 (2021). https://doi.org/10.1038/s41586-021-03819-2

MOLNFT Q8N1D0 research and analysis (ICN3D with VR)

FASTA sequences

>sp|Q8N1D0|BWR1B_HUMAN Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein OS=Homo sapiens OX=9606 GN=SLC22A18AS PE=1 SV=3 MGELPGSEGMWENCPLGWVKKKASGTLAPLDFLLQRKRLWLWASEPVRPQPQGIHRFREARRQFCRMRGSRLTGGRKGFGSSGLRFGRGGFSEEVMPQPVLKAMRCAEGAWWFSPDGPAGSAASIWPAEGAEGLPGQLGRDRLEVVYSVPDNVPGQNGSRRPLVCKITGKCLSVCSEENAKAGGCSAFPLLLSQLGARMTGREHAHKGPELTTPDSGLPRPPNPALAGFRALAQHSPPLGTSTPSAVLLSAAT