Structure of PDB 3fa3 Chain P Binding Site BS01
Receptor Information
>3fa3 Chain P (length=301) Species:
5061
(Aspergillus niger) [
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PMVTAATSLRRALENPDSFIVAPGVYDGLSARVALSAGFDALYMTGAGTA
ASVHGQADLGICTLNDMRANAEMISNISPSTPVIADADTGYGGPIMVART
TEQYSRSGVAAFHIEDQVQTKRCGHLAGKILVDTDTYVTRIRAAVQARQR
IGSDIVVIARTDSLQTHGYEESVARLRAARDAGADVGFLEGITSREMARQ
VIQDLAGWPLLLNMVEHGATPSISAAEAKEMGFRIIIFPFAALGPAVAAM
REAMEKLKRDGIPGLDKEMTPQMLFRVCGLDESMKVDAQAGGAAFDGGVD
L
Ligand information
Ligand ID
OAF
InChI
InChI=1S/C4H4F2O6/c5-3(6,1(7)8)4(11,12)2(9)10/h11-12H,(H,7,8)(H,9,10)
InChIKey
PNUBNHHFDUCRFW-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
FC(F)(C(=O)O)C(O)(O)C(=O)O
CACTVS 3.341
OC(=O)C(O)(O)C(F)(F)C(O)=O
OpenEye OEToolkits 1.5.0
C(=O)(C(C(C(=O)O)(F)F)(O)O)O
Formula
C4 H4 F2 O6
Name
2,2-difluoro-3,3-dihydroxybutanedioic acid
ChEMBL
DrugBank
ZINC
PDB chain
3fa3 Chain P Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3fa3
Structure and function of 2,3-dimethylmalate lyase, a PEP mutase/isocitrate lyase superfamily member.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
Y44 T46 G47 A48 D87 C124 G125 R161 E191 N214 P240
Binding residue
(residue number reindexed from 1)
Y43 T45 G46 A47 D86 C123 G124 R160 E190 N213 P239
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y44 T46 G47 A48 D59 D87 D89 H114 E116 K122 C124 G125 H126 R161 E191 N214 T221 S223
Catalytic site (residue number reindexed from 1)
Y43 T45 G46 A47 D58 D86 D88 H113 E115 K121 C123 G124 H125 R160 E190 N213 T220 S222
Enzyme Commision number
4.1.3.30
: methylisocitrate lyase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016787
hydrolase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:3fa3
,
PDBe:3fa3
,
PDBj:3fa3
PDBsum
3fa3
PubMed
19133276
UniProt
Q2L887
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