Structure of PDB 6bjb Chain B Binding Site BS01
Receptor Information
>6bjb Chain B (length=384) Species:
6253
(Ascaris suum) [
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RPITDVVFVGAARTPIGSFRSAFNNVPVTVLGREALKGALKNANVKPSLV
QEAFIGVVVPSNAGQGPARQVVLGAGCDVSTVVTAVNKMSASGMKAIACA
ASILQLDLQEMVVAGGMESMSCVPFYLPRGEIPFGGTKLIDGIPRDGLND
VYNDILMGACADKVAKQFAITREEQDKYAILSYKRSAAAWKEGIFAKEII
PLEVTITVEEDEEYKKVNFEKIPKLKPAFTSEGSVTAANASTLNDGAAMV
VMTTVDGAKKHGLKPLARMLAYGDAATHPIDFGIAPASVIPKVLKLAGLQ
IKDIDLWEINEAFAVVPLYTMKTLGLDESKVNIHGGAVSLGHPIGMSGAR
IVGHLVHTLKPGQKGCAAICNGGGGAGGMIIEKL
Ligand information
Ligand ID
1VU
InChI
InChI=1S/C24H40N7O17P3S/c1-4-15(33)52-8-7-26-14(32)5-6-27-22(36)19(35)24(2,3)10-45-51(42,43)48-50(40,41)44-9-13-18(47-49(37,38)39)17(34)23(46-13)31-12-30-16-20(25)28-11-29-21(16)31/h11-13,17-19,23,34-35H,4-10H2,1-3H3,(H,26,32)(H,27,36)(H,40,41)(H,42,43)(H2,25,28,29)(H2,37,38,39)/t13-,17-,18-,19+,23-/m1/s1
InChIKey
QAQREVBBADEHPA-IEXPHMLFSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CCC(=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
CACTVS 3.385
CCC(=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 12.01
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)CC
CACTVS 3.385
CCC(=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 1.7.6
CCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
Formula
C24 H40 N7 O17 P3 S
Name
propionyl Coenzyme A
ChEMBL
DrugBank
DB02912
ZINC
ZINC000008551120
PDB chain
6bjb Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6bjb
Structural and Biochemical Studies of Substrate Selectivity in Ascaris suum Thiolases.
Resolution
1.50001 Å
Binding residue
(original residue number in PDB)
S91 L149 M158 Y184 N224 K227 I228 L231 A243 A244 S247 F288 A318 F319 H348 C376 N377 G378
Binding residue
(residue number reindexed from 1)
S90 L148 M157 Y183 N218 K221 I222 L225 A237 A238 S241 F282 A312 F313 H342 C370 N371 G372
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S91 H348 C376 G378
Catalytic site (residue number reindexed from 1)
S90 H342 C370 G372
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003985
acetyl-CoA C-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
GO:0046872
metal ion binding
Biological Process
GO:0006635
fatty acid beta-oxidation
Cellular Component
GO:0005739
mitochondrion
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6bjb
,
PDBe:6bjb
,
PDBj:6bjb
PDBsum
6bjb
PubMed
29381332
UniProt
F1KYX0
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