Structure of PDB 3st8 Chain A Binding Site BS02
Receptor Information
>3st8 Chain A (length=475) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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DTAVLVLAAGPGTRMRSDTPKVLHTLAGRSMLSHVLHAIAKLAPQRLIVV
LGHDHQRIAPLVGELADTLGRTIDVALQDRPLGTGHAVLCGLSALPDDYA
GNVVVTSGDTPLLDADTLADLIATHRAVSAAVTVLTTTLDDPFGYGRILR
TQDHEVMAIVEQTDATPSQREIREVNAGVYAFDIAALRSALSRLSSNNAQ
QELYLTDVIAILRSDGQTVHASHVDDSALVAGVNNRVQLAELASELNRRV
VAAHQLAGVTVVDPATTWIDVDVTIGRDTVIHPGTQLLGRTQIGGRCVVG
PDTTLTDVAVGDGASVVRTHGSSSSIGDGAAVGPFTYLRPGTALGADGKL
GAFVEVKNSTIGTGTKVPHLTYVGDADIGEYSNIGASSVFVNYDGTSKRR
TTVGSHVRTGSDTMFVAPVTIGDGAYTGAGTVVREDVPPGALAVSAGPQR
NIENWVQRKRPGSPAAQASKRASEM
Ligand information
Ligand ID
COA
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCS
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
3st8 Chain A Residue 498 [
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Receptor-Ligand Complex Structure
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PDB
3st8
Structure of Mycobacterium tuberculosis GlmU in complex with Acetyl CoA
Resolution
1.98 Å
Binding residue
(original residue number in PDB)
G390 A391 G415 S416 G433 A434 V449 A451
Binding residue
(residue number reindexed from 1)
G385 A386 G410 S411 G428 A429 V444 A446
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:3st8
,
PDBe:3st8
,
PDBj:3st8
PDBsum
3st8
PubMed
UniProt
P9WMN3
|GLMU_MYCTU Bifunctional protein GlmU (Gene Name=glmU)
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