Structure of PDB 3x1j Chain C Binding Site BS01
Receptor Information
>3x1j Chain C (length=158) Species:
350703
(Pseudomonas aeruginosa 2192) [
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MNRVLYPGTFDPITKGHGDLIERASRLFDHVIIAVAASPKKNPLFSLEQR
VALAQEVTKHLPNVEVVGFSTLLAHFVKEQKANVFLRGLRAVSDFEYEFQ
LANMNRQLAPDVESMFLTPSEKYSFISSTLVREIAALGGDISKFVHPAVA
DALAERFK
Ligand information
Ligand ID
ACO
InChI
InChI=1S/C23H38N7O17P3S/c1-12(31)51-7-6-25-14(32)4-5-26-21(35)18(34)23(2,3)9-44-50(41,42)47-49(39,40)43-8-13-17(46-48(36,37)38)16(33)22(45-13)30-11-29-15-19(24)27-10-28-20(15)30/h10-11,13,16-18,22,33-34H,4-9H2,1-3H3,(H,25,32)(H,26,35)(H,39,40)(H,41,42)(H2,24,27,28)(H2,36,37,38)/t13-,16-,17-,18+,22-/m1/s1
InChIKey
ZSLZBFCDCINBPY-ZSJPKINUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(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)O
CACTVS 3.341
CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(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
ACDLabs 10.04
O=C(SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O)C
CACTVS 3.341
CC(=O)SCCNC(=O)CCNC(=O)[CH](O)C(C)(C)CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
Formula
C23 H38 N7 O17 P3 S
Name
ACETYL COENZYME *A
ChEMBL
CHEMBL1230809
DrugBank
ZINC
ZINC000008551095
PDB chain
3x1j Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
3x1j
Transition of phosphopantetheine adenylyltransferase from catalytic to allosteric state is characterized by ternary complex formation in Pseudomonas aeruginosa
Resolution
2.334 Å
Binding residue
(original residue number in PDB)
L130 E133 I134 L137
Binding residue
(residue number reindexed from 1)
L130 E133 I134 L137
Annotation score
2
Binding affinity
MOAD
: Ki=8.4uM
Enzymatic activity
Catalytic site (original residue number in PDB)
H17 K41 R90 S128
Catalytic site (residue number reindexed from 1)
H17 K41 R90 S128
Enzyme Commision number
2.7.7.3
: pantetheine-phosphate adenylyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004595
pantetheine-phosphate adenylyltransferase activity
GO:0005524
ATP binding
GO:0008771
[citrate (pro-3S)-lyase] ligase activity
GO:0016779
nucleotidyltransferase activity
Biological Process
GO:0009058
biosynthetic process
GO:0015937
coenzyme A biosynthetic process
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:3x1j
,
PDBe:3x1j
,
PDBj:3x1j
PDBsum
3x1j
PubMed
27041211
UniProt
A0A0X1KGP2
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