Structure of PDB 2nu8 Chain B Binding Site BS01
Receptor Information
>2nu8 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
2nu8 Chain B Residue 1325 [
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Receptor-Ligand Complex Structure
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PDB
2nu8
Participation of Cys 123alpha of Escherichia coli Succinyl-CoA Synthetase in Catalysis
Resolution
2.15 Å
Binding residue
(original residue number in PDB)
G320 G321 V323 R324 C325 I328 E350 N352
Binding residue
(residue number reindexed from 1)
G320 G321 V323 R324 C325 I328 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:2nu8
,
PDBe:2nu8
,
PDBj:2nu8
PDBsum
2nu8
PubMed
17642514
UniProt
P0A836
|SUCC_ECOLI Succinate--CoA ligase [ADP-forming] subunit beta (Gene Name=sucC)
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