Structure of PDB 2x98 Chain A Binding Site BS05
Receptor Information
>2x98 Chain A (length=430) Species:
478009
(Halobacterium salinarum R1) [
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ASPAANAIAYIVDGMGQTQISAARYLNAYKTAPERFPLNVSPAETPTGFD
AFSSRGSMTTFPDDPYETTTDSAAAATAFASGVKTYNGAIGGVQTSGGGF
QRVDTVLERASAQGYATGLITTTEATHATPAAFAAHVEDRGNQTEIARQY
IEETQPDVILGGQRRDFEADASNGGTLVDAARDNGYTIAETAAELDAVDD
PPVLGLFSQESHLDYYLDRKNDPENTQPNLDAMVDAGVDLLSSAGDPDKG
FFLLVESGRVDHAGHANYPAQVAEQYEATQVAGQLVEYAETTAEPTFLVS
TGDHECGGLTLGRDSPYEVEYDVLAAQKATTSRLRDLLAGVRSADELESI
VAAHTGITALTDREVAKLRDAPGSISTILAERAGIAFTTDGHTGTDVPVF
AHGPNAARFDAARDNTAVADALAAALGVSL
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
2x98 Chain A Residue 1478 [
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Receptor-Ligand Complex Structure
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PDB
2x98
Structural and Biochemical Characterization of a Halophilic Archaeal Alkaline Phosphatase.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
D282 S285
Binding residue
(residue number reindexed from 1)
D239 S242
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D56 S115 H170 T172 R183 E299 D304 H305 H308 D346 H347 H435
Catalytic site (residue number reindexed from 1)
D13 S72 H127 T129 R140 E256 D261 H262 H265 D303 H304 H392
Enzyme Commision number
3.1.3.1
: alkaline phosphatase.
Gene Ontology
Molecular Function
GO:0004035
alkaline phosphatase activity
GO:0016787
hydrolase activity
GO:0016791
phosphatase activity
GO:0046872
metal ion binding
Biological Process
GO:0016311
dephosphorylation
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2x98
,
PDBe:2x98
,
PDBj:2x98
PDBsum
2x98
PubMed
20438737
UniProt
B0R9W3
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