Structure of PDB 1i3m Chain B Binding Site BS02
Receptor Information
>1i3m Chain B (length=345) Species:
9606
(Homo sapiens) [
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AEKVLVTGGAGYIGSHTVLELLEAGYLPVVIDNFHNAFRGGGSLPESLRR
VQELTGRSVEFEEMDILDQGALQRLFKKYSFMAVIHFAGLKAMGESVQKP
LDYYRVNLTGTIQLLEIMKAHGVKNLVFSSSATVYGNPQYLPLDEAHPTG
GCTNPYGKSKFFIEEMIRDLCQADKTWNVVLLRYFNPTGAHASGCIGEDP
QGIPNNLMPYVSQVAIGRREALNVFGNDYDTEDGTGVRDYIHVVDLAKGH
IAALRKLKEQCGCRIYNLGTGTGYSVLQMVQAMEKASGKKIPYKVVARRE
GDVAACYANPSLAQEELGWTAALGLDRMCEDLWRWQKQNPSGFGT
Ligand information
Ligand ID
UD1
InChI
InChI=1S/C17H27N3O17P2/c1-6(22)18-10-13(26)11(24)7(4-21)35-16(10)36-39(31,32)37-38(29,30)33-5-8-12(25)14(27)15(34-8)20-3-2-9(23)19-17(20)28/h2-3,7-8,10-16,21,24-27H,4-5H2,1H3,(H,18,22)(H,29,30)(H,31,32)(H,19,23,28)/t7-,8-,10-,11-,12-,13-,14-,15-,16-/m1/s1
InChIKey
LFTYTUAZOPRMMI-CFRASDGPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)NC1C(C(C(OC1OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
CACTVS 3.341
CC(=O)N[CH]1[CH](O)[CH](O)[CH](CO)O[CH]1O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O
ACDLabs 10.04
O=P(OC1OC(C(O)C(O)C1NC(=O)C)CO)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
CACTVS 3.341
CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O
OpenEye OEToolkits 1.5.0
CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1O[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
Formula
C17 H27 N3 O17 P2
Name
URIDINE-DIPHOSPHATE-N-ACETYLGLUCOSAMINE
ChEMBL
CHEMBL388154
DrugBank
DB03397
ZINC
ZINC000008551100
PDB chain
1i3m Chain B Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
1i3m
Molecular basis for severe epimerase deficiency galactosemia. X-ray structure of the human V94m-substituted UDP-galactose 4-epimerase.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
Y157 N187 N206 N207 L208 N224 F226 R239 Y241 V277 R300 D303
Binding residue
(residue number reindexed from 1)
Y156 N186 N205 N206 L207 N223 F225 R238 Y240 V276 R299 D302
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S132 A133 T134 Y157 K161
Catalytic site (residue number reindexed from 1)
S131 A132 T133 Y156 K160
Enzyme Commision number
5.1.3.2
: UDP-glucose 4-epimerase.
5.1.3.7
: UDP-N-acetylglucosamine 4-epimerase.
Gene Ontology
Molecular Function
GO:0003974
UDP-N-acetylglucosamine 4-epimerase activity
GO:0003978
UDP-glucose 4-epimerase activity
GO:0016853
isomerase activity
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
Biological Process
GO:0006012
galactose metabolic process
GO:0019388
galactose catabolic process
GO:0033499
galactose catabolic process via UDP-galactose
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1i3m
,
PDBe:1i3m
,
PDBj:1i3m
PDBsum
1i3m
PubMed
11279193
UniProt
Q14376
|GALE_HUMAN UDP-glucose 4-epimerase (Gene Name=GALE)
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