Structure of PDB 1bs1 Chain A Binding Site BS01
Receptor Information
>1bs1 Chain A (length=224) Species:
562
(Escherichia coli) [
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SKRYFVTGTDTEVGKTVASCALLQAAKAAGYRTAGYKPVASGSEKTPEGL
RNSDALALQRNSSLQLDYATVNPYTFAEPTSPHIISAQEGRPIESLVMSA
GLRALEQQADWVLVEGAGGWFTPLSDTFTFADWVTQEQLPVILVVGVKLG
CINHAMLTAQVIQHAGLTLAGWVANDVTPPGKRHAEYMTTLTRMIPAPLL
GEIPWLAENPENAATGKYINLALL
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
1bs1 Chain A Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
1bs1
Crystal structure of two quaternary complexes of dethiobiotin synthetase, enzyme-MgADP-AlF3-diaminopelargonic acid and enzyme-MgADP-dethiobiotin-phosphate; implications for catalysis.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
T16 D54 E115
Binding residue
(residue number reindexed from 1)
T16 D54 E115
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T11 E12 K15 T16 K37 S41 D54 E115
Catalytic site (residue number reindexed from 1)
T11 E12 K15 T16 K37 S41 D54 E115
Enzyme Commision number
6.3.3.3
: dethiobiotin synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004141
dethiobiotin synthase activity
GO:0005524
ATP binding
GO:0016874
ligase activity
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
Biological Process
GO:0009102
biotin 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:1bs1
,
PDBe:1bs1
,
PDBj:1bs1
PDBsum
1bs1
PubMed
9865950
UniProt
P13000
|BIOD1_ECOLI ATP-dependent dethiobiotin synthetase BioD 1 (Gene Name=bioD1)
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