Structure of PDB 2ywr Chain A Binding Site BS03
Receptor Information
>2ywr Chain A (length=216) Species:
63363
(Aquifex aeolicus) [
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MLKIGVLVSGRGSNLQAIIDAIESGKVNASIELVISDNPKAYAIERCKKH
NVECKVIQRKEFPSKKEFEERMALELKKKGVELVVLAGFMRILSHNFLKY
FPNKVINIHPSLIPAFQGLHAQKQAVEFGVKFSGCTVHIVDESVDAGPVI
VQAVVPVLPEDDENTLADRILKWEHKILPQTVQWFAQDRIIIDGRKVIVK
DATYGTLPVNPALEIF
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
2ywr Chain A Residue 767 [
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Receptor-Ligand Complex Structure
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PDB
2ywr
Structures and reaction mechanisms of the two related enzymes, PurN and PurU.
Resolution
1.77 Å
Binding residue
(original residue number in PDB)
I44 K48 C54
Binding residue
(residue number reindexed from 1)
I44 K48 C54
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N107 H109 T136 D145
Catalytic site (residue number reindexed from 1)
N107 H109 T136 D145
Enzyme Commision number
2.1.2.2
: phosphoribosylglycinamide formyltransferase 1.
Gene Ontology
Molecular Function
GO:0004644
phosphoribosylglycinamide formyltransferase activity
GO:0016740
transferase activity
Biological Process
GO:0006164
purine nucleotide biosynthetic process
GO:0006189
'de novo' IMP biosynthetic process
GO:0009058
biosynthetic 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:2ywr
,
PDBe:2ywr
,
PDBj:2ywr
PDBsum
2ywr
PubMed
24108189
UniProt
O67023
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