Structure of PDB 5jbx Chain A Binding Site BS01

Receptor Information
>5jbx Chain A (length=258) Species: 246197 (Myxococcus xanthus DK 1622) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MPEFKVDARGPIEIWTIDGESRRNAISRAMLKELGELVTRVSSSRDVRAV
VITGAGDKAFCAGADLKERATMAEDEVRAFLDGLRRTFRAIEKSDCVFIA
AINGAALGGGTELALACDLRVAAPAAELGLTEVKLGIIPGGGGTQRLARL
VGPGRAKDLILTARRINAAEAFSVGLANRLAPEGHLLAVAYGLAESVVEN
APIAVATAKHAIDEGTGLELDDALALELRKYEEILKTEDRLEGLRAFAEK
RAPVYKGR
Ligand information
Ligand IDCOA
InChIInChI=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
InChIKeyRGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0CC(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 3.341CC(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 1.5.0CC(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 3.341CC(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 10.04O=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
FormulaC21 H36 N7 O16 P3 S
NameCOENZYME A
ChEMBLCHEMBL1213327
DrugBankDB01992
ZINCZINC000008551087
PDB chain5jbx Chain A Residue 301 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB5jbx The Structure of LiuC, a 3-Hydroxy-3-Methylglutaconyl CoA Dehydratase Involved in Isovaleryl-CoA Biosynthesis in Myxococcus xanthus, Reveals Insights into Specificity and Catalysis.
Resolution1.1 Å
Binding residue
(original residue number in PDB)
S21 R22 R23 A62 A64 D65 L66 L107 G108 T131 E132 L135
Binding residue
(residue number reindexed from 1)
S21 R22 R23 A62 A64 D65 L66 L107 G108 T131 E132 L135
Annotation score3
Enzymatic activity
Catalytic site (original residue number in PDB) A64 R69 L81 R85 G109 E112 T131 E132 I137 P139 G140 A225 L235
Catalytic site (residue number reindexed from 1) A64 R69 L81 R85 G109 E112 T131 E132 I137 P139 G140 A225 L235
Enzyme Commision number 4.2.1.55: 3-hydroxybutyryl-CoA dehydratase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0016829 lyase activity
GO:0016836 hydro-lyase activity
Biological Process
GO:0006635 fatty acid beta-oxidation

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:5jbx, PDBe:5jbx, PDBj:5jbx
PDBsum5jbx
PubMed27271456
UniProtQ1D5Y4

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