Structure of PDB 3n1t Chain A Binding Site BS01
Receptor Information
>3n1t Chain A (length=114) Species:
562
(Escherichia coli) [
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EETIFSKIIRREIPSDIVYQDDLVTAFRDISPQAPTHILIIPNILIPTVN
DVSAEHEQALGRMITVAAKIAEQEGIAEDGYRLIMNTNRHGGQEVYHIAM
HLLGGRPLGPMLAH
Ligand information
Ligand ID
5GP
InChI
InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
RQFCJASXJCIDSX-UUOKFMHZSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=C1c2ncn(c2N=C(N)N1)C3OC(C(O)C3O)COP(=O)(O)O
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)O)O)O)N=C(NC2=O)N
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N=C(NC2=O)N
Formula
C10 H14 N5 O8 P
Name
GUANOSINE-5'-MONOPHOSPHATE
ChEMBL
CHEMBL283807
DrugBank
DB01972
ZINC
ZINC000002159505
PDB chain
3n1t Chain A Residue 200 [
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Receptor-Ligand Complex Structure
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PDB
3n1t
Probing the Impact of the echinT C-Terminal Domain on Structure and Catalysis.
Resolution
1.716 Å
Binding residue
(original residue number in PDB)
I6 I10 D31 I32 L41 E96 V97 H103
Binding residue
(residue number reindexed from 1)
I4 I8 D29 I30 L39 E94 V95 H101
Annotation score
2
Enzymatic activity
Enzyme Commision number
3.9.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003824
catalytic activity
GO:0016787
hydrolase activity
GO:0042803
protein homodimerization activity
GO:0043530
adenosine 5'-monophosphoramidase activity
Biological Process
GO:0055130
D-alanine catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3n1t
,
PDBe:3n1t
,
PDBj:3n1t
PDBsum
3n1t
PubMed
20934431
UniProt
P0ACE7
|HINT_ECOLI Purine nucleoside phosphoramidase (Gene Name=hinT)
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