Structure of PDB 1cqj Chain D Binding Site BS02
Receptor Information
>1cqj Chain D (length=286) Species:
562
(Escherichia coli) [
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SILIDKNTKVICQGFTGSQGTFHSEQAIAYGTKMVGGVTPGKGGTTHLGL
PVFNTVREAVAATGATASVIYVPAPFCKDSILEAIDAGIKLIITITEGIP
TLDMLTVKVKLDEAGVRMIGPNCPGVITPGECKIGIQPGHIHKPGKVGIV
SRSGTLTYEAVKQTTDYGFGQSTCVGIGGDPIPGSNFIDILEMFEKDPQT
EAIVMIGEIGGSAEEEAAAYIKEHVTKPVVGYIAGVTAPKGKRMGHAGAI
IAGGKGTADEKFAALEAAGVKTVRSLADIGEALKTV
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
1cqj Chain D Residue 902 [
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Receptor-Ligand Complex Structure
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PDB
1cqj
ADP-binding site of Escherichia coli succinyl-CoA synthetase revealed by x-ray crystallography.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
G14 T16 S18 Q19 V38 P40 K42 V72 P73 T96 E97 C123 P124
Binding residue
(residue number reindexed from 1)
G14 T16 S18 Q19 V38 P40 K42 V72 P73 T96 E97 C123 P124
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
E208 H246
Catalytic site (residue number reindexed from 1)
E208 H246
Enzyme Commision number
6.2.1.5
: succinate--CoA ligase (ADP-forming).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003824
catalytic activity
GO:0004775
succinate-CoA ligase (ADP-forming) activity
GO:0004776
succinate-CoA ligase (GDP-forming) activity
GO:0005515
protein binding
GO:0016874
ligase activity
Biological Process
GO:0006099
tricarboxylic acid cycle
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0009361
succinate-CoA ligase complex (ADP-forming)
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1cqj
,
PDBe:1cqj
,
PDBj:1cqj
PDBsum
1cqj
PubMed
10625475
UniProt
P0AGE9
|SUCD_ECOLI Succinate--CoA ligase [ADP-forming] subunit alpha (Gene Name=sucD)
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