Structure of PDB 1rf4 Chain D Binding Site BS01
Receptor Information
>1rf4 Chain D (length=427) Species:
1313
(Streptococcus pneumoniae) [
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MKLKTNIRHLHGIIRVPGDKSISHRSIIFGSLAEGETKVYDILRGEDVLS
TMQVFRDLGVEIEDKDGVITVQGVGMAGLKAPQNALNMGNSGTSIRLISG
VLAGADFEVEMFGDDSLSKRPMDRVTLPLKKMGVSISGQTERDLPPLRLK
GTKNLRPIHYELPIASAQVKSALMFAALQAKGESVIIEKEYTRNHTEDML
QQFGGHLSVDGKKITVQGPQKLTGQKVVVPGDISSAAFWLVAGLIAPNSR
LVLQNVGINETRTGIIDVIRAMGGKLEITEIDPVAKSATLIVESSDLKGT
EICGALIPRLIDELPIIALLATQAQGVTVIKDAEELKVKETDRIQVVADA
LNSMGADITPTADGMIIKGKSALHGARVNTFGDHRIGMMTAIAALLVADG
EVELDRAEAINTSYPSFFDDLESLIHG
Ligand information
Ligand ID
SPQ
InChI
InChI=1S/C10H15FO14P2/c11-3-10(9(15)16,25-27(20,21)22)23-5-1-4(8(13)14)2-6(7(5)12)24-26(17,18)19/h2,5-7,12H,1,3H2,(H,13,14)(H,15,16)(H2,17,18,19)(H2,20,21,22)/t5-,6-,7+,10+/m1/s1
InChIKey
HTMVUWTXBMZROV-JQCUSGDOSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1[C@H]([C@@H]([C@@H](C=C1C(=O)O)OP(=O)(O)O)O)O[C@](CF)(C(=O)O)OP(=O)(O)O
ACDLabs 10.04
O=C(O)C(OP(=O)(O)O)(OC1CC(=CC(OP(=O)(O)O)C1O)C(=O)O)CF
CACTVS 3.341
O[C@H]1[C@@H](CC(=C[C@H]1O[P](O)(O)=O)C(O)=O)O[C@@](CF)(O[P](O)(O)=O)C(O)=O
OpenEye OEToolkits 1.5.0
C1C(C(C(C=C1C(=O)O)OP(=O)(O)O)O)OC(CF)(C(=O)O)OP(=O)(O)O
CACTVS 3.341
O[CH]1[CH](CC(=C[CH]1O[P](O)(O)=O)C(O)=O)O[C](CF)(O[P](O)(O)=O)C(O)=O
Formula
C10 H15 F O14 P2
Name
(3R,4S,5R)-5-{[(1R)-1-CARBOXY-2-FLUORO-1-(PHOSPHONOOXY)ETHYL]OXY}-4-HYDROXY-3-(PHOSPHONOOXY)CYCLOHEX-1-ENE-1-CARBOXYLIC ACID
ChEMBL
DrugBank
ZINC
ZINC000033821523
PDB chain
1rf4 Chain D Residue 1751 [
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Receptor-Ligand Complex Structure
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PDB
1rf4
Structural studies of Streptococcus pneumoniae EPSP synthase in unliganded state, tetrahedral intermediate-bound state and S3P-GLP-bound state.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
K20 S21 R25 G92 T93 R120 S166 Q168 R193 D312 K339 E340 R343 H384 R385
Binding residue
(residue number reindexed from 1)
K20 S21 R25 G92 T93 R120 S166 Q168 R193 D312 K339 E340 R343 H384 R385
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
K20 S21 D47 N90 D115 R120 D312 E340 H384 R385 T412
Catalytic site (residue number reindexed from 1)
K20 S21 D47 N90 D115 R120 D312 E340 H384 R385 T412
Enzyme Commision number
2.5.1.19
: 3-phosphoshikimate 1-carboxyvinyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003866
3-phosphoshikimate 1-carboxyvinyltransferase activity
GO:0005515
protein binding
GO:0016740
transferase activity
GO:0016765
transferase activity, transferring alkyl or aryl (other than methyl) groups
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009073
aromatic amino acid family biosynthetic process
GO:0009423
chorismate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1rf4
,
PDBe:1rf4
,
PDBj:1rf4
PDBsum
1rf4
PubMed
14763973
UniProt
Q9S400
|AROA_STRPN 3-phosphoshikimate 1-carboxyvinyltransferase (Gene Name=aroA)
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