Structure of PDB 5cnx Chain A Binding Site BS02
Receptor Information
>5cnx Chain A (length=360) Species:
83333
(Escherichia coli K-12) [
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STLLASLRDWLKAQQLDAVLLSSRQNKQPHLGISTGSGYVVISRESAHIL
VDSRYYVEVEARAQGYQLHLLDATNTLTTIVNQIIADEQLQTLGFEGQQV
SWETAHRWQSELNAKLVSATPDVLRQIKTPEEVEKIRLACGIADRGAEHI
RRFIQAGMSEREIAAELEWFMRQQGAEKASFDTIVASGWRGALPHGKASD
KIVAAGEFVTLDFGALYQGYCSDMTRTLLVNGEGVSAESHLLFNVYQIVL
QAQLAAISAIRPGVRCQQVDDAARRVITEAGYGDYFGHNTGHAIGIEVHE
DPRFSPRDTTTLQPGMLLTVEPGIYLPGQGGVRIEDVVLVTPQGAEVLYA
MPKTVLLTGE
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
5cnx Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5cnx
Structures and activities of widely conserved small prokaryotic aminopeptidases-P clarify classification of M24B peptidases
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
D212 D223 E335
Binding residue
(residue number reindexed from 1)
D212 D223 E335
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H195 D212 D223 T225 H288 H292 H299 E321 Y325 R333 E335
Catalytic site (residue number reindexed from 1)
H195 D212 D223 T225 H288 H292 H299 E321 Y325 R333 E335
Enzyme Commision number
3.4.11.-
Gene Ontology
Molecular Function
GO:0004177
aminopeptidase activity
GO:0005515
protein binding
GO:0008235
metalloexopeptidase activity
GO:0042803
protein homodimerization activity
GO:0046914
transition metal ion binding
GO:0070006
metalloaminopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:5cnx
,
PDBe:5cnx
,
PDBj:5cnx
PDBsum
5cnx
PubMed
30536999
UniProt
P76524
|YPDF_ECOLI Aminopeptidase YpdF (Gene Name=ypdF)
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