Structure of PDB 1gup Chain B Binding Site BS03
Receptor Information
>1gup Chain B (length=344) Species:
562
(Escherichia coli) [
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TQFNPVDHPHRRYNPLTGQWILVSPHRAKRPWQGAQETPAKQVLPAHDPD
CFLCAGNVRVTGDKNPDYTGTYVFTNDFAALMSDTPDAPESHDPLMRCQS
ARGTSRVICFSPDHSKTLPELSVAALTEIVKTWQEQTAELGKTYPWVQVF
ENKGAAMGCSNPHPGGQIWANSFLPNEAEREDRLQKEYFAEQKSPMLVDY
VQRELADGSRTVVETEHWLAVVPYWAAWPFETLLLPKAHVLRITDLTDAQ
RSDLALALKKLTSRYDNLFQCSFPYSMGWHGAPFNGEENQHWQLHAHFYP
PLLRSATVRKFMVGYEMLAETQRDLTAEQAAERLRAVSDIHFRE
Ligand information
Ligand ID
GDU
InChI
InChI=1S/C15H24N2O17P2/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25)/t5-,6-,8+,9-,10+,11-,12-,13-,14-/m1/s1
InChIKey
HSCJRCZFDFQWRP-ABVWGUQPSA-N
SMILES
Software
SMILES
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)O)O)O)O)O
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]1O
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]1O
ACDLabs 10.04
O=P(OC1OC(C(O)C(O)C1O)CO)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
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)O)O)O)O)O
Formula
C15 H24 N2 O17 P2
Name
GALACTOSE-URIDINE-5'-DIPHOSPHATE;
UDP-D-GALACTOPYRANOSE
ChEMBL
CHEMBL439009
DrugBank
DB03501
ZINC
ZINC000008551104
PDB chain
1gup Chain B Residue 352 [
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Receptor-Ligand Complex Structure
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PDB
1gup
Structural analysis of the H166G site-directed mutant of galactose-1-phosphate uridylyltransferase complexed with either UDP-glucose or UDP-galactose: detailed description of the nucleotide sugar binding site.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
F53 V61 N77 D78 F151 N153 G159 C160 S161 Q168 W170
Binding residue
(residue number reindexed from 1)
F52 V60 N76 D77 F150 N152 G158 C159 S160 Q167 W169
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C52 C55 H115 N153 S161 H164 G166 Q168
Catalytic site (residue number reindexed from 1)
C51 C54 H114 N152 S160 H163 G165 Q167
Enzyme Commision number
2.7.7.12
: UDP-glucose--hexose-1-phosphate uridylyltransferase.
Gene Ontology
Molecular Function
GO:0004335
galactokinase activity
GO:0008108
UDP-glucose:hexose-1-phosphate uridylyltransferase activity
GO:0008198
ferrous iron binding
GO:0008270
zinc ion binding
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0006012
galactose metabolic process
GO:0033499
galactose catabolic process via UDP-galactose
GO:0046835
carbohydrate phosphorylation
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:1gup
,
PDBe:1gup
,
PDBj:1gup
PDBsum
1gup
PubMed
9063869
UniProt
P09148
|GAL7_ECOLI Galactose-1-phosphate uridylyltransferase (Gene Name=galT)
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