Structure of PDB 1pjx Chain A Binding Site BS01
Receptor Information
>1pjx Chain A (length=314) Species:
6622
(Loligo vulgaris) [
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MEIPVIEPLFTKVTEDIPGAEGPVFDKNGDFYIVAPEVEVNGKPAGEILR
IDLKTGKKTVICKPEVNGYGGIPAGCQCDRDANQLFVADMRLGLLVVQTD
GTFEEIAKKDSEGRRMQGCNDCAFDYEGNLWITAPAGEVAPADYTRSMQE
KFGSIYCFTTDGQMIQVDTAFQFPNGIAVRHMNDGRPYQLIVAETPTKKL
WSYDIKGPAKIENKKVWGHIPGTHEGGADGMDFDEDNNLLVANWGSSHIE
VFGPDGGQPKMRIRCPFEKPSNLHFKPQTKTIFVTEHENNAVWKFEWQRN
GKKQYCETLKFGIF
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1pjx Chain A Residue 491 [
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Receptor-Ligand Complex Structure
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PDB
1pjx
Statistical analysis of crystallographic data obtained from squid ganglion DFPase at 0.85 A resolution.
Resolution
0.85 Å
Binding residue
(original residue number in PDB)
E21 N120 N175 D229
Binding residue
(residue number reindexed from 1)
E21 N120 N175 D229
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E21 E37 N120 N175 D229 H287
Catalytic site (residue number reindexed from 1)
E21 E37 N120 N175 D229 H287
Enzyme Commision number
3.8.2.2
: diisopropyl-fluorophosphatase.
Gene Ontology
Molecular Function
GO:0005509
calcium ion binding
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
GO:0047862
diisopropyl-fluorophosphatase activity
Biological Process
GO:0008150
biological_process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1pjx
,
PDBe:1pjx
,
PDBj:1pjx
PDBsum
1pjx
PubMed
14501113
UniProt
Q7SIG4
|DFPA_LOLVU Diisopropyl-fluorophosphatase
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