Structure of PDB 1d1q Chain A Binding Site BS01
Receptor Information
>1d1q Chain A (length=159) Species:
4932
(Saccharomyces cerevisiae) [
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IEKPKISVAFIALGNFCRSPMAEAIFKHEVEKANLENRFNKIDSFGTSNY
HVGESPDHRTVSICKQHGVKINHKGKQIKTKHFDEYDYIIGMDESNINNL
KKIQPEGSKAKVCLFGDWNTNDGTVQTIIEDPWYGDIQDFEYNFKQITYF
SKQFLKKEL
Ligand information
Ligand ID
4NP
InChI
InChI=1S/C6H6NO6P/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12/h1-4H,(H2,10,11,12)
InChIKey
XZKIHKMTEMTJQX-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
O[P](O)(=O)Oc1ccc(cc1)[N+]([O-])=O
ACDLabs 10.04
O=P(Oc1ccc(cc1)[N+]([O-])=O)(O)O
OpenEye OEToolkits 1.5.0
c1cc(ccc1[N+](=O)[O-])OP(=O)(O)O
Formula
C6 H6 N O6 P
Name
4-NITROPHENYL PHOSPHATE
ChEMBL
CHEMBL24231
DrugBank
DB04214
ZINC
ZINC000001529638
PDB chain
1d1q Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
1d1q
Crystal structures of a low-molecular weight protein tyrosine phosphatase from Saccharomyces cerevisiae and its complex with the substrate p-nitrophenyl phosphate.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
A13 L14 G15 N16 F17 C18 R19 D132 W134
Binding residue
(residue number reindexed from 1)
A12 L13 G14 N15 F16 C17 R18 D131 W133
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
A13 N16 C18 R19 S20 D132
Catalytic site (residue number reindexed from 1)
A12 N15 C17 R18 S19 D131
Enzyme Commision number
3.1.3.2
: acid phosphatase.
3.1.3.48
: protein-tyrosine-phosphatase.
Gene Ontology
Molecular Function
GO:0003993
acid phosphatase activity
GO:0004721
phosphoprotein phosphatase activity
GO:0004725
protein tyrosine phosphatase activity
Biological Process
GO:0006470
protein dephosphorylation
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1d1q
,
PDBe:1d1q
,
PDBj:1d1q
PDBsum
1d1q
PubMed
10684639
UniProt
P40347
|PPAL_YEAST Low molecular weight phosphotyrosine protein phosphatase (Gene Name=LTP1)
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