Structure of PDB 2nu7 Chain B Binding Site BS02
Receptor Information
>2nu7 Chain B (length=388) Species:
562
(Escherichia coli) [
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MNLHEYQAKQLFARYGLPAPVGYACTTPREAEEAASKIGAGPWVVKCQVH
AGGRGKAGGVKVVNSKEDIRAFAENWLGKRLVTYQTDANGQPVNQILVEA
ATDIAKELYLGAVVDRSSRRVVFMASTEGGVEIEKVAEETPHLIHKVALD
PLTGPMPYQGRELAFKLGLEGKLVQQFTKIFMGLATIFLERDLALIEINP
LVITKQGDLICLDGKLGADGNALFRQPDLREMRDQSQEDPREAQAAQWEL
NYVALDGNIGCMVNGAGLAMGTMDIVKLHGGEPANFLDVGGGATKERVTE
AFKIILSDDKVKAVLVNIFGGIVRCDLIADGIIGAVAEVGVNVPVVVRLE
GNNAELGAKKLADSGLNIIAAKGLTDAAQQVVAAVEGK
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
2nu7 Chain B Residue 1325 [
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Receptor-Ligand Complex Structure
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PDB
2nu7
Participation of Cys 123alpha of Escherichia coli Succinyl-CoA Synthetase in Catalysis
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G320 I322 V323 C325 L349 E350 N352
Binding residue
(residue number reindexed from 1)
G320 I322 V323 C325 L349 E350 N352
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
Y109 E197
Catalytic site (residue number reindexed from 1)
Y109 E197
Enzyme Commision number
6.2.1.5
: succinate--CoA ligase (ADP-forming).
Gene Ontology
Molecular Function
GO:0000287
magnesium ion 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:0005524
ATP binding
GO:0016874
ligase activity
GO:0046872
metal ion binding
Biological Process
GO:0006099
tricarboxylic acid cycle
GO:0006104
succinyl-CoA metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0009361
succinate-CoA ligase complex (ADP-forming)
GO:0042709
succinate-CoA ligase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2nu7
,
PDBe:2nu7
,
PDBj:2nu7
PDBsum
2nu7
PubMed
17642514
UniProt
P0A836
|SUCC_ECOLI Succinate--CoA ligase [ADP-forming] subunit beta (Gene Name=sucC)
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