Structure of PDB 5jbx Chain A Binding Site BS01
Receptor Information
>5jbx Chain A (length=258) Species:
246197
(Myxococcus xanthus DK 1622) [
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MPEFKVDARGPIEIWTIDGESRRNAISRAMLKELGELVTRVSSSRDVRAV
VITGAGDKAFCAGADLKERATMAEDEVRAFLDGLRRTFRAIEKSDCVFIA
AINGAALGGGTELALACDLRVAAPAAELGLTEVKLGIIPGGGGTQRLARL
VGPGRAKDLILTARRINAAEAFSVGLANRLAPEGHLLAVAYGLAESVVEN
APIAVATAKHAIDEGTGLELDDALALELRKYEEILKTEDRLEGLRAFAEK
RAPVYKGR
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
5jbx Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5jbx
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.
Resolution
1.1 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 score
3
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
PDBsum
5jbx
PubMed
27271456
UniProt
Q1D5Y4
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