Structure of PDB 8p5w Chain F Binding Site BS03
Receptor Information
>8p5w Chain F (length=1119) Species:
196627
(Corynebacterium glutamicum ATCC 13032) [
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PGQTPIRGIFKSIAKNMDISLEIPTATSVRDMPARLMFENRAMVNDQLKR
TRGGKISFTHIIGYAMVKAVMAHPDMNNSYDVIDGKPTLIVPEHINLGLA
IDLPQKDGSRALVVAAIKETEKMNFSEFLAAYEDIVARSRKGKLTMDDYQ
GVTVSLTNPGGIGTRHSVPRLTKGQGTIIGVGSMDYPAEFQGASEDRLAE
LGVGKLVTITSTYDHRVIQGAVSGEFLRTMSRLLTDDSFWDEIFDAMNVP
YTPMRWAQDVPNTGVDKNTRVMQLIEAYRSRGHLIADTNPLSWVQPGMPV
PDHRDLDIETHNLTIWDLDRTFNVGGFGGKETMTLREVLSRLRAAYTLKV
GSEYTHILDRDERTWLQDRLEAGMPKPTQAEQKYILQKLNAAEAFENFLQ
TKYVGQKRFSLEGAEALIPLMDSAIDTAAGQGLDEVVIGMPHRGRLNVLF
NIVGKPLASIFNEFEGQMEQGQIGGSGDVKYHLGSEGQHLQMFGDGEIKV
SLTANPSHLEAVNPVMEGIVRAKQDYLDKGVDGKTVVPLLLHGDAAFAGL
GIVPETINLAKLRGYDVGGTIHIVVNNQIGFTTTPDSSRSMHYATDYAKA
FGCPVFHVNGDDPEAVVWVGQLATEYRRRFGKDVFIDLVCYRLRGHNEAD
DPSMTQPKMYELITGRETVRAQYTEDLLGRGDLSNEDAEAVVRDFHDQME
SVFNEVKEGGKKQAEAQTGITGSQKLPHGLETNISREELLELGQAFANTP
EGFNYHPRVAPVAKKRVSSVTEGGIDWAWGELLAFGSLANSGRLVRLAGE
DSRRGTFTQRHAVAIDPATAEEFNPLHELAQSKGNNGKFLVYNSALTEYA
GMGFEYGYSVGNEDSIVAWEAQFGDFANGAQTIIDEYVSSGEAKWGQTSK
LILLLPHGYEGQGPDHSSARIERFLQLCAEGSMTVAQPSTPANHFHLLRR
HALSDLKRPLVIFTPKSMLRNKAAASAPEDFTEVTKFQSVINDPNVADAA
KVKKVMLVSGKLYYELAKRKEKDGRDDIAIVRIEMLHPIPFNRISEALAG
YPNAEEVLFVQDEPANQGPWPFYQEHLPELIPNMPKMRRVSRRAQSSTAT
GVAKVHQLEEKQLIDEAFE
Ligand information
Ligand ID
ACO
InChI
InChI=1S/C23H38N7O17P3S/c1-12(31)51-7-6-25-14(32)4-5-26-21(35)18(34)23(2,3)9-44-50(41,42)47-49(39,40)43-8-13-17(46-48(36,37)38)16(33)22(45-13)30-11-29-15-19(24)27-10-28-20(15)30/h10-11,13,16-18,22,33-34H,4-9H2,1-3H3,(H,25,32)(H,26,35)(H,39,40)(H,41,42)(H2,24,27,28)(H2,36,37,38)/t13-,16-,17-,18+,22-/m1/s1
InChIKey
ZSLZBFCDCINBPY-ZSJPKINUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(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)O
CACTVS 3.341
CC(=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 10.04
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)C
CACTVS 3.341
CC(=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 1.5.0
CC(=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
Formula
C23 H38 N7 O17 P3 S
Name
ACETYL COENZYME *A
ChEMBL
CHEMBL1230809
DrugBank
ZINC
ZINC000008551095
PDB chain
8p5w Chain F Residue 1302 [
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Receptor-Ligand Complex Structure
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PDB
8p5w
High resolution cryo-EM and crystallographic snapshots of the actinobacterial two-in-one 2-oxoglutarate dehydrogenase.
Resolution
2.26 Å
Binding residue
(original residue number in PDB)
P828 G830 G1032 R1051 K1087 P1139 I1140 P1141 F1142 N1143 R1144
Binding residue
(residue number reindexed from 1)
P727 G729 G931 R950 K986 P1038 I1039 P1040 F1041 N1042 R1043
Annotation score
3
Enzymatic activity
Enzyme Commision number
1.2.4.2
: oxoglutarate dehydrogenase (succinyl-transferring).
2.3.1.61
: dihydrolipoyllysine-residue succinyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004149
dihydrolipoyllysine-residue succinyltransferase activity
GO:0004591
oxoglutarate dehydrogenase (succinyl-transferring) activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016624
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor
GO:0016746
acyltransferase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
Biological Process
GO:0006099
tricarboxylic acid cycle
Cellular Component
GO:0005829
cytosol
GO:0045252
oxoglutarate dehydrogenase complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:8p5w
,
PDBe:8p5w
,
PDBj:8p5w
PDBsum
8p5w
PubMed
37563123
UniProt
Q8NRC3
|ODO12_CORGL 2-oxoglutarate dehydrogenase E1/E2 component (Gene Name=odhA)
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