Structure of PDB 1fuq Chain B Binding Site BS02

Receptor Information
>1fuq Chain B (length=455) Species: 562 (Escherichia coli) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MNTVRSEKDSMGAIDVPADKLWGAQTQRSLEHFRISTEKMPTSLIHALAL
TKRAAAKVNEDLGLLSEEKASAIRQAADEVLAGQHDDEFPLAIWQTGSGT
QSNMNMNEVLANRASELLGGVRGMERKVHPNDDVNKSQSSNDVFPTAMHV
AALLALRKQLIPQLKTLTQTLNEKSRAFADIVKIGRTHLQDATPLTLGQE
ISGWVAMLEHNLKHIEYSLPHVAELALGGTAVGTGLNTHPEYARRVADEL
AVITCAPFVTAPNKFEALATCDALVQAHGALKGLAASLMKIANDVRWLAS
GPRCGIGEISIPENEPMPGKVNPTQCEALTMLCCQVMGNDVAINMGGASG
NFELNVFRPMVIHNFLQSVRLLADGMESFNKHCAVGIEPNRERINQLLNE
SLMLVTALNTHIGYDKAAEIAKKAHKEGLTLKAAALALGYLSEAEFDSWV
RPEQM
Ligand information
Ligand IDCIT
InChIInChI=1S/C6H8O7/c7-3(8)1-6(13,5(11)12)2-4(9)10/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)
InChIKeyKRKNYBCHXYNGOX-UHFFFAOYSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0C(C(=O)O)C(CC(=O)O)(C(=O)O)O
ACDLabs 10.04O=C(O)CC(O)(C(=O)O)CC(=O)O
CACTVS 3.341OC(=O)CC(O)(CC(O)=O)C(O)=O
FormulaC6 H8 O7
NameCITRIC ACID
ChEMBLCHEMBL1261
DrugBankDB04272
ZINCZINC000000895081
PDB chain1fuq Chain B Residue 1002 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB1fuq Crystallographic studies of the catalytic and a second site in fumarase C from Escherichia coli.
Resolution2.0 Å
Binding residue
(original residue number in PDB)
T100 S140
Binding residue
(residue number reindexed from 1)
T100 S140
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) N107 T187 H188 K324 E331
Catalytic site (residue number reindexed from 1) N107 T187 H188 K320 E327
Enzyme Commision number 4.2.1.2: fumarate hydratase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0004333 fumarate hydratase activity
GO:0016829 lyase activity
GO:0042802 identical protein binding
Biological Process
GO:0006099 tricarboxylic acid cycle
GO:0006106 fumarate metabolic process
GO:0006108 malate metabolic process
GO:0006979 response to oxidative stress
Cellular Component
GO:0005737 cytoplasm

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:1fuq, PDBe:1fuq, PDBj:1fuq
PDBsum1fuq
PubMed8909293
UniProtP05042|FUMC_ECOLI Fumarate hydratase class II (Gene Name=fumC)

[Back to BioLiP]