Structure of PDB 5bz4 Chain K Binding Site BS01
Receptor Information
>5bz4 Chain K (length=400) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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RDAVICEPVRTPIGRYGGMFRSLTAVDLGVTALKGLLERTGIAADQVEDV
ILGHCYPNSEAPAIGRVVALDAGLPITVPGMQVDRRCGSGLQAVIQACLQ
VRSGDHDLVVAGGAESMSNVAFYSTDMRWGGARTGVQIHDGLARGRTTAG
GKFHPVPGGMLETAENLRREYHISRTEQDELAVRSHQRAVAAQSEGVLAE
EIIPVPVRTEETISVDEHPRADTTVEALAKLKPVLLKQDPEATVTAGNSS
GQNDAASMCIVTTPEKAAELGLKPLVRLVSWGSAGVAPDLMGIGPVPATE
VALAKAGLTLADIDLIELNEAFAAQALAVMREWKFGEADHERTNVRGSGI
SLGHPVGATGGRMLATLARELHRREARYGLETMCIGGGQGLAAVFERVQE
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
5bz4 Chain K Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5bz4
Structural characterization of a mitochondrial 3-ketoacyl-CoA (T1)-like thiolase from Mycobacterium smegmatis
Resolution
2.43 Å
Binding residue
(original residue number in PDB)
C90 R149 M163 R226 A252 G253 S256 Q258 M297 A327 F328 H360
Binding residue
(residue number reindexed from 1)
C87 R146 M160 R220 A246 G247 S250 Q252 M291 A321 F322 H354
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
C90 H360 C390 G392
Catalytic site (residue number reindexed from 1)
C87 H354 C384 G386
Enzyme Commision number
2.3.1.9
: acetyl-CoA C-acetyltransferase.
Gene Ontology
Molecular Function
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
View graph for
Molecular Function
External links
PDB
RCSB:5bz4
,
PDBe:5bz4
,
PDBj:5bz4
PDBsum
5bz4
PubMed
26627655
UniProt
A0QUH3
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