Structure of PDB 5vk4 Chain B Binding Site BS02
Receptor Information
>5vk4 Chain B (length=330) Species:
485
(Neisseria gonorrhoeae) [
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DAGDQLVEKIKPFAKRTMRPEVLGDLGGFGALVEIGKKYQNPVLVSGTDG
VGTKLKLAFDWDKHDTVGIDLVAMSVNDILVQGAEPLFFLDYFACGKLDV
PRATDVIKGIAQGCEESGCALIGGETAEMPGMYPVGEYDLAGFAVGVVEK
ENVITGLSVGAGDMVLGLASNGAHSNGYSLIRKIIERDNPDLDAEFDNGK
TLREAVIAPTRLYVKPILAALEKFTIKGMAHITGGGITENVPRVLPKNTV
AQIDAESWELPKLFQWLQKAGNVETQEMYRTFNCGIGMVVIVAAEDADAV
RSFLSGQGETVYRLGCIRERQGNEHQTQVA
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
5vk4 Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5vk4
Crystal structure of a phosphoribosylformylglycinamidine cyclo-ligase from Neisseria gonorrhoeae bound to AMPPNP and magnesium
Resolution
2.65 Å
Binding residue
(original residue number in PDB)
E139 T140
Binding residue
(residue number reindexed from 1)
E125 T126
Annotation score
1
Enzymatic activity
Enzyme Commision number
6.3.3.1
: phosphoribosylformylglycinamidine cyclo-ligase.
Gene Ontology
Molecular Function
GO:0004637
phosphoribosylamine-glycine ligase activity
GO:0004641
phosphoribosylformylglycinamidine cyclo-ligase activity
GO:0005524
ATP binding
GO:0016874
ligase activity
Biological Process
GO:0006164
purine nucleotide biosynthetic process
GO:0006189
'de novo' IMP biosynthetic process
GO:0046084
adenine 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:5vk4
,
PDBe:5vk4
,
PDBj:5vk4
PDBsum
5vk4
PubMed
UniProt
Q5F973
|PUR5_NEIG1 Phosphoribosylformylglycinamidine cyclo-ligase (Gene Name=purM)
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