Structure of PDB 2fzk Chain A Binding Site BS01
Receptor Information
>2fzk Chain A (length=310) Species:
562
(Escherichia coli) [
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ANPLYQKHIISINDLSRDDLNLVLATAAKLKANPQPELLKHKVIASCFFE
ASTRTRLSFETSMHRLGASVVGFSDSANTSLGKKGETLADTISVISTYVD
AIVMRHPQEGAARLATEFSGNVPVLNAGDGSNQHPTQTLLDLFTIQETQG
RLDNLHVAMVGDLKYGRTVHSLTQALAKFDGNRFYFIAPDALAMPQYILD
MLDEKGIAWSLHSSIEEVMAEVDILYMTRVQKERLDPSEYANVKAQFVLR
ASDLHNAKANMKVLHPLPRVDEIATDVDKTPHAWYFQQAGNGIFARQALL
ALVLNRDLVL
Ligand information
Ligand ID
EOZ
InChI
InChI=1S/C11H14N2O10P2/c14-9(4-24(18,19)20)12-7-1-6(11(16)17)2-8(3-7)13-10(15)5-25(21,22)23/h1-3H,4-5H2,(H,12,14)(H,13,15)(H,16,17)(H2,18,19,20)(H2,21,22,23)
InChIKey
LGLZCZRWQTWLGU-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC(=O)c1cc(NC(=O)C[P](O)(O)=O)cc(NC(=O)C[P](O)(O)=O)c1
OpenEye OEToolkits 1.5.0
c1c(cc(cc1NC(=O)CP(=O)(O)O)NC(=O)CP(=O)(O)O)C(=O)O
ACDLabs 10.04
O=C(Nc1cc(cc(c1)NC(=O)CP(=O)(O)O)C(=O)O)CP(=O)(O)O
Formula
C11 H14 N2 O10 P2
Name
3,5-BIS[(PHOSPHONOACETYL)AMINO]BENZOIC ACID
ChEMBL
DrugBank
ZINC
ZINC000024799743
PDB chain
2fzk Chain A Residue 611 [
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Receptor-Ligand Complex Structure
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PDB
2fzk
T-state Inhibitors of E. coli Aspartate Transcarbamoylase that Prevent the Allosteric Transition.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
T55 H134 Q137 T168 R229 P266 L267 R296
Binding residue
(residue number reindexed from 1)
T55 H134 Q137 T168 R229 P266 L267 R296
Annotation score
1
Binding affinity
MOAD
: Ki=310uM
PDBbind-CN
: -logKd/Ki=3.60,Ki=250uM
Enzymatic activity
Catalytic site (original residue number in PDB)
R54 T55 K84 R105 H134 Q137 T228 P266 G292
Catalytic site (residue number reindexed from 1)
R54 T55 K84 R105 H134 Q137 T228 P266 G292
Enzyme Commision number
2.1.3.2
: aspartate carbamoyltransferase.
Gene Ontology
Molecular Function
GO:0004070
aspartate carbamoyltransferase activity
GO:0004088
carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity
GO:0005515
protein binding
GO:0016597
amino acid binding
GO:0016740
transferase activity
GO:0016743
carboxyl- or carbamoyltransferase activity
GO:0042802
identical protein binding
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0006520
amino acid metabolic process
GO:0006541
glutamine metabolic process
GO:0044205
'de novo' UMP biosynthetic process
GO:0070207
protein homotrimerization
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0009347
aspartate carbamoyltransferase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2fzk
,
PDBe:2fzk
,
PDBj:2fzk
PDBsum
2fzk
PubMed
16906764
UniProt
P0A786
|PYRB_ECOLI Aspartate carbamoyltransferase catalytic subunit (Gene Name=pyrB)
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