Structure of PDB 4n54 Chain A Binding Site BS01
Receptor Information
>4n54 Chain A (length=340) Species:
543734
(Lacticaseibacillus casei BL23) [
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KTIKIGIVGLGRLGKIHATNIATKIQHAKLQAATSVVPAELDWAKKELGV
EEVFEDFDDMVQHADIDAVFIVSPSGFHLQQIESALNAGKHVFSEKPIGL
DIEAIEHTQQVIAQHANLKFQLGFMRRFDDSYRYAKQLVDQGKIGDITLI
RSYSIDPAAGMASFVKFATSANSGGLFLDMSIHDIDVIRWFTGKEIDKVW
AIGLNRAYPVLDKAGELETGAALMQLEDKTMAILVAGRNAAHGYHVETEI
IGTKGMLRIAQVPEKNLVTVMNEEGIIRPTSQNFPERFAQAFLSEEQAFV
NSILNNQDVGITAEDGLQGTKAALALQEAFEKNDIVQVAS
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
4n54 Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4n54
Crystal structure of scyllo-inositol dehydrogenase from Lactobacillus casei with bound cofactor NAD(H) and scyllo-inositol
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
V11 G12 L13 G14 R15 L16 S38 V39 E43 S76 P77 F80 H81 E98 K99 M128 F170 F287
Binding residue
(residue number reindexed from 1)
V8 G9 L10 G11 R12 L13 S35 V36 E40 S73 P74 F77 H78 E95 K96 M125 F167 F284
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K99 H186
Catalytic site (residue number reindexed from 1)
K96 H183
Enzyme Commision number
1.1.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
Biological Process
GO:0006740
NADPH regeneration
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4n54
,
PDBe:4n54
,
PDBj:4n54
PDBsum
4n54
PubMed
UniProt
A0A0J9X1Y7
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