Structure of PDB 3spt Chain A Binding Site BS03
Receptor Information
>3spt Chain A (length=474) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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DTAVLVLAAGPGTRMRSDTPKVLHTLAGRSMLSHVLHAIAKLAPQRLIVV
LGHDHQRIAPLVGELADTLGRTIDVALQDRPLGTGHAVLCGLSALPDDYA
GNVVVTSGDTPLLDADTLADLIATHRAVSAAVTVLTTTLDDPFGYGRILR
TQDHEVMAIVEQTDATPSQREIREVNAGVYAFDIAALRSALSRLSSNNAQ
QELYLTDVIAILRSDGQTVHASHVDDSALVAGVNNRVQLAELASELNRRV
VAAHQLAGVTVVDPATTWIDVDVTIGRDTVIHPGTQLLGRTQIGGRCVVG
PDTTLTDVAVGDGASVVRTHGSSSSIGDGAAVGPFTYLRPGTALGADGKL
GAFVEVKNSTIGTGTKVPHLTYVGDADIGEYSNIGASSVFVNYDGTSKRR
TTVGSHVRTGSDTMFVAPVTIGDGAYTGAGTVVREDVPPGALAVSAGPQR
NIENWVQRKRPGSPAAQASKRASE
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
3spt Chain A Residue 498 [
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Receptor-Ligand Complex Structure
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PDB
3spt
Structure of Mycobacterium tuberculosis GlmU in complex with Acetyl CoA
Resolution
2.33 Å
Binding residue
(original residue number in PDB)
L12 A13 A14 G15 Q83 P86 G88 T89 A92 D114 Y150 G151 E166 N181 T211 N239
Binding residue
(residue number reindexed from 1)
L7 A8 A9 G10 Q78 P81 G83 T84 A87 D109 Y145 G146 E161 N176 T206 N234
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
R19
Catalytic site (residue number reindexed from 1)
R14
Enzyme Commision number
2.3.1.157
: glucosamine-1-phosphate N-acetyltransferase.
2.7.7.23
: UDP-N-acetylglucosamine diphosphorylase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003977
UDP-N-acetylglucosamine diphosphorylase activity
GO:0005515
protein binding
GO:0016746
acyltransferase activity
GO:0016779
nucleotidyltransferase activity
GO:0019134
glucosamine-1-phosphate N-acetyltransferase activity
GO:0046872
metal ion binding
GO:0070569
uridylyltransferase activity
Biological Process
GO:0000902
cell morphogenesis
GO:0006048
UDP-N-acetylglucosamine biosynthetic process
GO:0008360
regulation of cell shape
GO:0009245
lipid A biosynthetic process
GO:0009252
peptidoglycan biosynthetic process
GO:0035635
entry of bacterium into host cell
GO:0044650
adhesion of symbiont to host cell
GO:0071555
cell wall organization
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3spt
,
PDBe:3spt
,
PDBj:3spt
PDBsum
3spt
PubMed
UniProt
P9WMN3
|GLMU_MYCTU Bifunctional protein GlmU (Gene Name=glmU)
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