Structure of PDB 2qt3 Chain A Binding Site BS01
Receptor Information
>2qt3 Chain A (length=401) Species:
47660
(Pseudomonas sp. ADP) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
KDFDLIIRNAYLSEKDSVYDIGIVGDRIIKIEAKIEGTVKDEIDAKGNLV
SPGFVDAHTHMDKSFTSTGERLPKFWSRPYTRDAAIEDGLKYYKNATHEE
IKRHVIEHAHMQVLHGTLYTRTHVDVDSVAKTKAVEAVLEAKEELKDLID
IQVVAFAQSGFFVDLESESLIRKSLDMGCDLVGGVDPATRENNVEGSLDL
CFKLAKEYDVDIDYHIHDIGTVGVYSINRLAQKTIENGYKGRVTTSHAWC
FADAPSEWLDEAIPLYKDSGMKFVTCFSSTPPTMPVIKLLEAGINLGCAS
DNIRDFWVPFGNGDMVQGALIETQRLELKTNRDLGLIWKMITSEGARVLG
IEKNYGIEVGKKADLVVLNSLSPQWAIIDQAKRLCVIKNGRIIVKDEVIV
A
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2qt3 Chain A Residue 501 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2qt3
Crystal structure of N-Isopropylammelide isopropylaminohydrolase AtzC from Pseudomonas sp. strain ADP complexed with Zn.
Resolution
2.24 Å
Binding residue
(original residue number in PDB)
H60 H62 H217
Binding residue
(residue number reindexed from 1)
H58 H60 H215
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H60 H62 Q160 H217 D220 D303
Catalytic site (residue number reindexed from 1)
H58 H60 Q158 H215 D218 D301
Enzyme Commision number
3.5.4.42
: N-isopropylammelide isopropylaminohydrolase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0016810
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
GO:0016814
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines
GO:0018764
N-isopropylammelide isopropylaminohydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0019381
atrazine catabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2qt3
,
PDBe:2qt3
,
PDBj:2qt3
PDBsum
2qt3
PubMed
UniProt
O52063
|ATZC_PSESD N-isopropylammelide isopropyl amidohydrolase (Gene Name=atzC)
[
Back to BioLiP
]