Structure of PDB 4qro Chain H Binding Site BS01

Receptor Information
>4qro Chain H (length=324) Species: 296591 (Polaromonas sp. JS666) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MNGKIALEEHFATEETLMDSAGFVPDKDWPELRSRLLDIQDRRVRLMDEH
GIETMILSLNAPAVQAIADSTRANETARRANDFLAEQVAKQPTRFRGFAA
LPMQDPELAARELERCVKELGFVGALVNGFSQDNRSAVPLYYDMAQYWPF
WETVQALDVPFYLHPRNPLPSDARIYDGHAWLLGPTWAFGQETAVHALRL
MGSGLFDKYPALKIILGHMGEGLPYSMWRIDHRNAWIKTTPKYPAKRKIV
DYFNENFYLTTSGNFRTQTLIDAILEIGADRILFSTDWPFENIDHAADWF
ENTSISEADRKKIGWGNAQNLFKL
Ligand information
Ligand IDMN
InChIInChI=1S/Mn/q+2
InChIKeyWAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341[Mn++]
FormulaMn
NameMANGANESE (II) ION
ChEMBL
DrugBankDB06757
ZINC
PDB chain4qro Chain H Residue 402 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4qro Crystal Structure of Dihydroxybenzoate Decarboxylase from Frompolaromonas Sp WITH BOUND MANGANESE AND 2-NITRORESORCINOL
Resolution1.65 Å
Binding residue
(original residue number in PDB)
E8 H10 H164 D287
Binding residue
(residue number reindexed from 1)
E8 H10 H164 D287
Annotation score1
Enzymatic activity
Enzyme Commision number 4.1.1.103: gamma-resorcylate decarboxylase.
Gene Ontology
Molecular Function
GO:0016787 hydrolase activity
GO:0016831 carboxy-lyase activity
GO:0046872 metal ion binding
Biological Process
GO:0019748 secondary metabolic 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:4qro, PDBe:4qro, PDBj:4qro
PDBsum4qro
PubMed
UniProtQ12BV1|GRDC_POLSJ Gamma-resorcylate decarboxylase (Gene Name=Bpro_2061)

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