Structure of PDB 3bp1 Chain D Binding Site BS02
Receptor Information
>3bp1 Chain D (length=256) Species:
243277
(Vibrio cholerae O1 biovar El Tor str. N16961) [
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YANQYDPSLLQPVPRSLNRNDLHLSATLPFQGCDIWTLYELSWLNQKGLP
QVAIGEVSIPATSANLIESKSFKLYLNSYNQTRFASWDEVQTRLVHDLSA
CAGETVTVNVKSLNEYTAEPIVTMQGECIDDQDIEIANYEFDDALLQGAA
QGEEVSEVLHSHLLKSNQPDWGSVEIAYHGAKMNREALLRYLVSFREHNE
FHEQCVERIFTDIMRYCQPQSLTVYARYTRRGGLDINPFRSSHQSAPNHN
QRMARQ
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
3bp1 Chain D Residue 289 [
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Receptor-Ligand Complex Structure
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PDB
3bp1
High-resolution structure of the nitrile reductase QueF combined with molecular simulations provide insight into enzyme mechanism.
Resolution
1.53 Å
Binding residue
(original residue number in PDB)
Y65 D266 R283 Q287
Binding residue
(residue number reindexed from 1)
Y39 D235 R252 Q256
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D201 H233 E234
Catalytic site (residue number reindexed from 1)
D170 H202 E203
Enzyme Commision number
1.7.1.13
: preQ1 synthase.
Gene Ontology
Molecular Function
GO:0003674
molecular_function
GO:0016491
oxidoreductase activity
GO:0033739
preQ1 synthase activity
GO:0046857
oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor
Biological Process
GO:0006400
tRNA modification
GO:0008150
biological_process
GO:0008616
queuosine biosynthetic process
Cellular Component
GO:0005575
cellular_component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3bp1
,
PDBe:3bp1
,
PDBj:3bp1
PDBsum
3bp1
PubMed
20875425
UniProt
Q9KTK0
|QUEF_VIBCH NADPH-dependent 7-cyano-7-deazaguanine reductase (Gene Name=queF)
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