Structure of PDB 2ywr Chain A Binding Site BS03

Receptor Information
>2ywr Chain A (length=216) Species: 63363 (Aquifex aeolicus) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MLKIGVLVSGRGSNLQAIIDAIESGKVNASIELVISDNPKAYAIERCKKH
NVECKVIQRKEFPSKKEFEERMALELKKKGVELVVLAGFMRILSHNFLKY
FPNKVINIHPSLIPAFQGLHAQKQAVEFGVKFSGCTVHIVDESVDAGPVI
VQAVVPVLPEDDENTLADRILKWEHKILPQTVQWFAQDRIIIDGRKVIVK
DATYGTLPVNPALEIF
Ligand information
Ligand IDCO
InChIInChI=1S/Co/q+2
InChIKeyXLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341[Co++]
FormulaCo
NameCOBALT (II) ION
ChEMBL
DrugBankDB14205
ZINC
PDB chain2ywr Chain A Residue 767 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2ywr Structures and reaction mechanisms of the two related enzymes, PurN and PurU.
Resolution1.77 Å
Binding residue
(original residue number in PDB)
I44 K48 C54
Binding residue
(residue number reindexed from 1)
I44 K48 C54
Annotation score1
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
PDBsum2ywr
PubMed24108189
UniProtO67023

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