Structure of PDB 4lis Chain A Binding Site BS02
Receptor Information
>4lis Chain A (length=364) Species:
227321
(Aspergillus nidulans FGSC A4) [
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PSGSVLVTGGTGYIGSFTTLALLEAGYKVVVADNLYNSSAEALNRIELIS
GKKAEFAQLDVTDEAAFDKVFEAHPDIDSVIHFAALKAVGESGEKPLDYY
HVNVYGTICLLRSMVRHNVTNIVFSSSATVYGDATRFPDMIPIPEHCPLG
PTNPYGNTKFAIELAITDVINAQRNNAKKAGNETEAAKWNGALLRYFNPA
GAHPSGIMGEDPQGVPYNLLPLLAQVATGKREKLLVFGDDYASHDGTAIR
DYIHILDLADGHLKALNYLRANNPGVRAWNLGTGRGSTVYEMIRAFSKAV
GRDLPYEVAPRRAGDVLNLTSNPTRANTELGWKAQRTLEQACEDLWLWTK
NNPQGYRQQPPAEL
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/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/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[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
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[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
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
4lis Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4lis
Elucidation of Substrate Specificity in Aspergillus nidulans UDP-Galactose-4-Epimerase.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
G13 Y14 I15 D34 N35 N38 S39 D61 V62 F84 A86 K88 S128 Y156 K160 Y197 P200
Binding residue
(residue number reindexed from 1)
G12 Y13 I14 D33 N34 N37 S38 D60 V61 F83 A85 K87 S127 Y155 K159 Y196 P199
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S128 A129 T130 Y156 K160
Catalytic site (residue number reindexed from 1)
S127 A128 T129 Y155 K159
Enzyme Commision number
5.1.3.2
: UDP-glucose 4-epimerase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003978
UDP-glucose 4-epimerase activity
GO:0016853
isomerase activity
Biological Process
GO:0006012
galactose metabolic process
GO:0033499
galactose catabolic process via UDP-galactose
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4lis
,
PDBe:4lis
,
PDBj:4lis
PDBsum
4lis
PubMed
24116166
UniProt
C8VAU8
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