Structure of PDB 1now Chain A Binding Site BS01 |
>1now Chain A (length=480) Species: 9606 (Homo sapiens)
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ALWPLPLSVKMTPNLLHLAPENFYISHSPNSTAGPSCTLLEEAFRRYHGY IFGTQVQQLLVSITLQSECDAFPNISSDESYTLLVKEPVAVLKANRVWGA LRGLETFSQLVYQDSYGTFTINESTIIDSPRFSHRGILIDTSRHYLPVKI ILKTLDAMAFNKFNVLHWHIVDDQSFPYQSITFPELSNKGSYSLSHVYTP NDVRMVIEYARLRGIRVLPEFDTPGHTLSWGKGQKDLLTPCYSLDSFGPI NPTLNTTYSFLTTFFKEISEVFPDQFIHLGGDEVEFKCWESNPKIQDFMR QKGFGTDFKKLESFYIQKVLDIIATINKGSIVWQEVFDDKAKLAPGTIVE VWKDSAYPEELSRVTASGFPVILSAPWYLDLISYGQDWRKYYKVEPLDFG GTQKQKQLFIGGEACLWGEYVDATNLTPRLWPRASAVGERLWSSKDVRDM DDAYDRLTRHRCRMVERGIAAQPLYAGYCN |
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Ligand ID | IFG |
InChI | InChI=1S/C8H16N2O4/c1-4(12)10-8-7(14)6(13)5(3-11)2-9-8/h5-9,11,13-14H,2-3H2,1H3,(H,10,12)/t5-,6+,7+,8-/m1/s1 |
InChIKey | IWVRQJNSUOIUFV-VGRMVHKJSA-N |
SMILES | Software | SMILES |
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OpenEye OEToolkits 1.5.0 | CC(=O)NC1C(C(C(CN1)CO)O)O | ACDLabs 10.04 | O=C(NC1NCC(CO)C(O)C1O)C | CACTVS 3.341 | CC(=O)N[C@H]1NC[C@H](CO)[C@H](O)[C@@H]1O | OpenEye OEToolkits 1.5.0 | CC(=O)N[C@@H]1[C@H]([C@H]([C@H](CN1)CO)O)O | CACTVS 3.341 | CC(=O)N[CH]1NC[CH](CO)[CH](O)[CH]1O |
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Formula | C8 H16 N2 O4 |
Name | (2R,3R,4S,5R)-2-ACETAMIDO-3,4-DIHYDROXY-5-HYDROXYMETHYL-PIPERIDINE |
ChEMBL | |
DrugBank | DB03861 |
ZINC |
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PDB chain | 1now Chain A Residue 557
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Catalytic site (original residue number in PDB) |
D354 E355 |
Catalytic site (residue number reindexed from 1) |
D282 E283 |
Enzyme Commision number |
3.2.1.52: beta-N-acetylhexosaminidase. |
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