Structure of PDB 5h63 Chain D Binding Site BS02
Receptor Information
>5h63 Chain D (length=302) Species:
562
(Escherichia coli) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
GHVSFAGIDYPLLPLNHQTPLVFQWFERNPDRFGQNEIPIINTQKNPYLN
NIINAAIIEKERIIGIFVDGDFSKGQRKALGKLEQNYRNIKVIYNSDLNY
SMYDKKLTTIYLENITKLEAQSASERDEVLLNGVKKSLEDVLKNNPEETL
ISSHNKDKGHLWFDFYRNLFLLKGSDAFLEAGKPGCHHLQPGGGCIYLDA
DMLLTDKLGTLYLPDGIAIHVSRKDNHVSLENGIIAVNRSEHPALIKGLE
IMHSKPYGDPYNDWLSKGLRHYFDGSHIQDYDAFCDFIEFKHENIIMNTS
SL
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
5h63 Chain D Residue 401 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
5h63
Structural basis for arginine glycosylation of host substrates by bacterial effector proteins.
Resolution
1.92 Å
Binding residue
(original residue number in PDB)
Q64 W65 F66 Y88 F203 D204 R207 D239 D241 E271 N272 G273 N338 S340
Binding residue
(residue number reindexed from 1)
Q24 W25 F26 Y48 F163 D164 R167 D199 D201 E231 N232 G233 N298 S300
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.4.1.-
Gene Ontology
Molecular Function
GO:0016757
glycosyltransferase activity
GO:0046872
metal ion binding
GO:0090729
toxin activity
GO:0106362
protein-arginine N-acetylglucosaminyltransferase activity
Biological Process
GO:0035821
modulation of process of another organism
Cellular Component
GO:0005576
extracellular region
GO:0043657
host cell
GO:0044177
host cell Golgi apparatus
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5h63
,
PDBe:5h63
,
PDBj:5h63
PDBsum
5h63
PubMed
30327479
UniProt
Q8ZNP4
|SSEK2_SALTY Protein-arginine N-acetylglucosaminyltransferase SseK2 (Gene Name=sseK2)
[
Back to BioLiP
]