Structure of PDB 3v7p Chain A Binding Site BS01
Receptor Information
>3v7p Chain A (length=409) Species:
387092
(Nitratiruptor sp. SB155-2) [
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MRIIKPFAILTPQTIIQDKAVAFDKKIEAIDTVENLIKKYPNAAVEHDEN
SLLLPGFANPHLHLEFSANKATLQYGDFIPWLYSVIRHREDLLPLCDGAC
LEQTLSSIIQTGTTAIGAISSYGEDLQACIDSALKVVYFNEVIGSNAATA
DVMYASFLERFHQSKKHENERFKAAVAIHSPYSVHYILAKRALDIAKKYG
SLVSVHFMESRAEREWLDKGSGEFAKFFKEFLNQTRPVNDTKSFLELFKE
LHTLFVHMVWANEEEIQTIASYNAHIIHCPISNRLLGNGVLDLEKIKSIP
YAIATDGLSSNYSLNMYEELKAALFVHPNKEATTFAKELIIRATKAGYDA
LGFEGGEIAVGKDADMQLIDLPEGLTNVEDLYLHVILHTTKPKKVYIQGE
EHVRNLYFQ
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
3v7p Chain A Residue 429 [
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Receptor-Ligand Complex Structure
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PDB
3v7p
Crystal Structure of Amidohydrolase Nis_0429 (Target Efi-500319) from Nitratiruptor Sp. Sb155-2
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
H61 H63 H206 D306
Binding residue
(residue number reindexed from 1)
H61 H63 H206 D306
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.5.4.40
: aminodeoxyfutalosine deaminase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0016810
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
GO:0046872
metal ion binding
Biological Process
GO:0009234
menaquinone biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3v7p
,
PDBe:3v7p
,
PDBj:3v7p
PDBsum
3v7p
PubMed
UniProt
A6Q234
|MQNX_NITSB Aminodeoxyfutalosine deaminase (Gene Name=NIS_0429)
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