Structure of PDB 1pt8 Chain A Binding Site BS01
Receptor Information
>1pt8 Chain A (length=416) Species:
562
(Escherichia coli) [
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MSTPLQGIKVLDFTGVQSGPSCTQMLAWFGADVIKIERPGVGDVTRHQLR
DIPDIDALYFTMLNSNKRSIELNTKTAEGKEVMEKLIREADILVENFHPG
AIDHMGFTWEHIQEINPRLIFGSIKGFDECSPYVNVKAYENVAQAAGGAA
STTGFWDGPPLVSAAALGDSNTGMHLLIGLLAALLHREKTGRGQRVTMSM
QDAVLNLCRVKLRDQQRLDKLGYLEEYPQYPNGTFGDAVPRGGNAGGGGQ
PGWILKCKGWETDPNAYIYFTIQEQNWENTCKAIGKPEWITDPAYSTAHA
RQPHIFDIFAEIEKYTVTIDKHEAVAYLTQFDIPCAPVLSMKEISLDPSL
RQSGSVVEVEQPLRGKYLTVGCPMKFSAFTPDIKAAPLLGEHTAAVLQEL
GYSDDEIAAMKQNHAI
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
1pt8 Chain A Residue 751 [
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Receptor-Ligand Complex Structure
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PDB
1pt8
The crystal structure of the Escherichia coli yfdW gene product reveals a new fold of two interlaced rings identifying a wide family of CoA transferases.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
V16 Q17 S18 R38 T74 K75 N96 F97 H98 K137 A138 D169 M200
Binding residue
(residue number reindexed from 1)
V16 Q17 S18 R38 T74 K75 N96 F97 H98 K137 A138 D169 M200
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
Q17 E140 D169 G248 G249
Catalytic site (residue number reindexed from 1)
Q17 E140 D169 G248 G249
Enzyme Commision number
2.8.3.16
: formyl-CoA transferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008410
CoA-transferase activity
GO:0016740
transferase activity
GO:0033608
formyl-CoA transferase activity
Biological Process
GO:0033611
oxalate catabolic process
GO:0071468
cellular response to acidic pH
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1pt8
,
PDBe:1pt8
,
PDBj:1pt8
PDBsum
1pt8
PubMed
12844490
UniProt
P69902
|FCTA_ECOLI Formyl-CoA:oxalate CoA-transferase (Gene Name=frc)
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