Structure of PDB 1ixe Chain D Binding Site BS01
Receptor Information
>1ixe Chain D (length=366) Species:
274
(Thermus thermophilus) [
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VARGLEGVLFTESRMCYIDGQQGKLYYYGIPIQELAEKSSFEETTFLLLH
GRLPRRQELEEFSAALARRRALPAHLLESFKRYPVSAHPMSFLRTAVSEF
GMLDPTEGDISREALYEKGLDLIAKFATIVAANKRLKEGKEPIPPREDLS
HAANFLYMANGVEPSPEQARLMDAALILHAEHGFNASTFTAIAAFSTETD
LYSAITAAVASLKGPRHGGANEAVMRMIQEIGTPERAREWVREKLAKKER
IMGMGHRVYKAFDPRAGVLEKLARLKEYQILKIVEEEAGKVLNPRGIYPN
VDFYSGVVYSDLGFSLEFFTPIFAVARISGWVGHILEYQELDNRLLRPGA
KYVGELDVPYVPLEAR
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
1ixe Chain D Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
1ixe
Structural comparison between the open and closed forms of citrate synthase from Thermus thermophilus HB8.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
R252 I253 G255 M256 G257 H258 R259 I307 N310
Binding residue
(residue number reindexed from 1)
R250 I251 G253 M254 G255 H256 R257 I297 N300
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S189 H219 H258 R267 D312
Catalytic site (residue number reindexed from 1)
S187 H217 H256 R265 D302
Enzyme Commision number
2.3.3.16
: citrate synthase (unknown stereospecificity).
Gene Ontology
Molecular Function
GO:0004108
citrate (Si)-synthase activity
GO:0016740
transferase activity
GO:0036440
citrate synthase activity
GO:0046912
acyltransferase activity, acyl groups converted into alkyl on transfer
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006099
tricarboxylic acid cycle
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1ixe
,
PDBe:1ixe
,
PDBj:1ixe
PDBsum
1ixe
PubMed
27493854
UniProt
Q5SIM6
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