Structure of PDB 1uda Chain A Binding Site BS02
Receptor Information
>1uda Chain A (length=338) Species:
562
(Escherichia coli) [
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MRVLVTGGSGYIGSHTCVQLLQNGHDVIILDNLCNSKRSVLPVIERLGGK
HPTFVEGDIRNEALMTEILHDHAIDTVIHFAGLKAVGESVQKPLEYYDNN
VNGTLRLISAMRAANVKNFIFSSSATVYGDNPKIPYVESFPTGTPQSPYG
KSKLMVEQILTDLQKAQPDWSIALLRYFNPVGAHPSGDMGEDPQGIPNNL
MPYIAQVAVGRRDSLAIFGNDYPTEDGTGVRDYIHVMDLADGHVVAMEKL
ANKPGVHIYNLGAGVGNSVLDVVNAFSKACGKPVNYHFAPRREGDLPAYW
ADASKADRELNWRVTRTLDEMAQDTWHWQSRHPQGYPD
Ligand information
Ligand ID
UFG
InChI
InChI=1S/C15H23FN2O16P2/c16-8-5(3-19)32-14(12(24)10(8)22)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)18-2-1-7(20)17-15(18)25/h1-2,5-6,8-14,19,21-24H,3-4H2,(H,26,27)(H,28,29)(H,17,20,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1
InChIKey
OAPPZHVTNHJVAL-JZMIEXBBSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)CO)F)O)O)O)O
ACDLabs 10.04
O=P(OC1OC(C(F)C(O)C1O)CO)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
CACTVS 3.341
OC[C@H]1O[C@H](O[P@@](O)(=O)O[P@@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O)[C@H](O)[C@@H](O)[C@@H]1F
CACTVS 3.341
OC[CH]1O[CH](O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O)[CH](O)[CH](O)[CH]1F
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)(O)O[P@@](=O)(O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)F)O)O)O)O
Formula
C15 H23 F N2 O16 P2
Name
URIDINE-5'-DIPHOSPHATE-4-DEOXY-4-FLUORO-ALPHA-D-GALACTOSE
ChEMBL
CHEMBL593125
DrugBank
DB04097
ZINC
ZINC000016051558
PDB chain
1uda Chain A Residue 341 [
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Receptor-Ligand Complex Structure
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PDB
1uda
Structural analysis of UDP-sugar binding to UDP-galactose 4-epimerase from Escherichia coli.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
T126 N179 N199 L200 A216 I217 F218 R231 Y233 R292 D295 Y299
Binding residue
(residue number reindexed from 1)
T126 N179 N199 L200 A216 I217 F218 R231 Y233 R292 D295 Y299
Annotation score
3
Binding affinity
MOAD
: Ki=1.4mM
Enzymatic activity
Catalytic site (original residue number in PDB)
S124 A125 T126 Y149 K153 M189
Catalytic site (residue number reindexed from 1)
S124 A125 T126 Y149 K153 M189
Enzyme Commision number
5.1.3.2
: UDP-glucose 4-epimerase.
Gene Ontology
Molecular Function
GO:0003978
UDP-glucose 4-epimerase activity
GO:0005515
protein binding
GO:0016853
isomerase activity
GO:0016857
racemase and epimerase activity, acting on carbohydrates and derivatives
GO:0042802
identical protein binding
GO:0070403
NAD+ binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006012
galactose metabolic process
GO:0009242
colanic acid biosynthetic process
GO:0033499
galactose catabolic process via UDP-galactose
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1uda
,
PDBe:1uda
,
PDBj:1uda
PDBsum
1uda
PubMed
9174344
UniProt
P09147
|GALE_ECOLI UDP-glucose 4-epimerase (Gene Name=galE)
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