Structure of PDB 1i5o Chain B Binding Site BS02
Receptor Information
>1i5o Chain B (length=153) Species:
562
(Escherichia coli) [
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MTHDNKLQVEAIKRGTVIDHIPAQIGFKLLSLFKLTETDQRITIGLNLPS
GEMGRKDLIKIENTFLSEDQVDQLALYAPQATVNRIDNYEVVGKSRPSLP
ERIDNVLVCPNSNCISHAEPVSSSFAVRKRANDIALKCKYCEKEFSHNVV
LAN
Ligand information
Ligand ID
PAL
InChI
InChI=1S/C6H10NO8P/c8-4(2-16(13,14)15)7-3(6(11)12)1-5(9)10/h3H,1-2H2,(H,7,8)(H,9,10)(H,11,12)(H2,13,14,15)/t3-/m0/s1
InChIKey
ZZKNRXZVGOYGJT-VKHMYHEASA-N
SMILES
Software
SMILES
CACTVS 3.341
OC(=O)C[CH](NC(=O)C[P](O)(O)=O)C(O)=O
CACTVS 3.341
OC(=O)C[C@H](NC(=O)C[P](O)(O)=O)C(O)=O
ACDLabs 10.04
O=C(NC(C(=O)O)CC(=O)O)CP(=O)(O)O
OpenEye OEToolkits 1.5.0
C(C(C(=O)O)NC(=O)CP(=O)(O)O)C(=O)O
OpenEye OEToolkits 1.5.0
C([C@@H](C(=O)O)NC(=O)CP(=O)(O)O)C(=O)O
Formula
C6 H10 N O8 P
Name
N-(PHOSPHONACETYL)-L-ASPARTIC ACID
ChEMBL
CHEMBL504802
DrugBank
DB03459
ZINC
ZINC000001563934
PDB chain
1i5o Chain B Residue 998 [
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Receptor-Ligand Complex Structure
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PDB
1i5o
Direct structural evidence for a concerted allosteric transition in Escherichia coli aspartate transcarbamoylase.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
M1 V91
Binding residue
(residue number reindexed from 1)
M1 V91
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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:1i5o
,
PDBe:1i5o
,
PDBj:1i5o
PDBsum
1i5o
PubMed
11323717
UniProt
P0A7F3
|PYRI_ECOLI Aspartate carbamoyltransferase regulatory chain (Gene Name=pyrI)
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