Structure of PDB 4ubu Chain A Binding Site BS01
Receptor Information
>4ubu Chain A (length=391) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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MGYPVIVEATRSPIGKRNGWLSGLHATELLGAVQKAVVDKAGIQSGLHAG
DVEQVIGGCVTQFGEQSNNISRVAWLTAGLPEHVGATTVDCQCGSGQQAN
HLIAGLIAAGAIDVGIACGIEAMSRVGLGANAGPDRSLIRAQSWDIDLPN
QFEAAERIAKRRGITREDVDVFGLESQRRAQRAWAEGRFDREISPIQAPV
LDEQNQPTGERRLVFRDQGLRETTMAGLGELKPVLEGGIHTAGTSSQISD
GAAAVLWMDEAVARAHGLTPRARIVAQALVGAEPYYHLDGPVQSTAKVLE
KAGMKIGDIDIVEINEAFASVVLSWARVHEPDMDRVNVNGGAIALGHPVG
CTGSRLITTALHELERTDQSLALITMCAGGALSTGTIIERI
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
4ubu Chain A Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
4ubu
FadA5 a Thiolase from Mycobacterium tuberculosis: A Steroid-Binding Pocket Reveals the Potential for Drug Development against Tuberculosis.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
S93 L128 Q151 F152 R221 G227 L231 A242 S246 V349
Binding residue
(residue number reindexed from 1)
S93 L128 Q151 F152 R221 G227 L231 A242 S246 V349
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
C93 H347 C377 G379
Catalytic site (residue number reindexed from 1)
C93 H347 C377 G379
Enzyme Commision number
2.3.1.16
: acetyl-CoA C-acyltransferase.
Gene Ontology
Molecular Function
GO:0003988
acetyl-CoA C-acyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
GO:0042802
identical protein binding
Biological Process
GO:0006635
fatty acid beta-oxidation
GO:0006707
cholesterol catabolic process
GO:0008203
cholesterol metabolic process
GO:0010124
phenylacetate catabolic process
GO:0016042
lipid catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4ubu
,
PDBe:4ubu
,
PDBj:4ubu
PDBsum
4ubu
PubMed
25482540
UniProt
I6XHI4
|FADA5_MYCTU Steroid 3-ketoacyl-CoA thiolase (Gene Name=fadA5)
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