Structure of PDB 1alj Chain A Binding Site BS03
Receptor Information
>1alj Chain A (length=446) Species:
562
(Escherichia coli) [
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MPVLENRAAQGDITAPGGARRLTGDQTAALRDSLSDKPAKNIILLIGDGM
GDSEITAARNYAEGAGGFFKGIDALPLTGQYTHYALNKKTGKPDYVTDSA
ASATAWSTGVKTYNGALGVDIHEKDHPTILEMAKAAGLATGNVSTAELQD
ATPAALVAHVTSRKCYGPSATSEKCPGNALEKGGKGSITEQLLNARADVT
LGGGAKTFAETATAGEWQGKTLREQAQARGYQLVSDAASLNSVTEANQQK
PLLGLFADGNMPVRWLGPKATYHGNIDKPAVTCTPNPQRNDSVPTLAQMT
DKAIELLSKNEKGFFLQVEGASIDKQDHAANPCGQIGETVDLDEAVQRAL
EFAKKEGNTLVIVTADHAHASQIVAPDTKAPGLTQALNTKDGAVMVMSYG
NSEEDSQENTGSQLRIAAYGPHAANVVGLTDQTDLFYTMKAALGLK
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
1alj Chain A Residue 453 [
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Receptor-Ligand Complex Structure
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PDB
1alj
Escherichia coli alkaline phosphatase: X-ray structural studies of a mutant enzyme (His-412-->Asn) at one of the catalytically important zinc binding sites.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
D101 S102 R166 H331 H370 N412
Binding residue
(residue number reindexed from 1)
D98 S99 R163 H328 H367 N409
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D51 S102 D153 T155 R166 E322 D327 K328 H331 D369 H370 N412
Catalytic site (residue number reindexed from 1)
D48 S99 D150 T152 R163 E319 D324 K325 H328 D366 H367 N409
Enzyme Commision number
3.1.3.1
: alkaline phosphatase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004035
alkaline phosphatase activity
GO:0004721
phosphoprotein phosphatase activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0016791
phosphatase activity
GO:0030613
oxidoreductase activity, acting on phosphorus or arsenic in donors
GO:0033748
hydrogenase (acceptor) activity
GO:0046872
metal ion binding
Biological Process
GO:0006470
protein dephosphorylation
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0042597
periplasmic space
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1alj
,
PDBe:1alj
,
PDBj:1alj
PDBsum
1alj
PubMed
8520475
UniProt
P00634
|PPB_ECOLI Alkaline phosphatase (Gene Name=phoA)
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