Structure of PDB 2gg0 Chain A Binding Site BS02
Receptor Information
>2gg0 Chain A (length=262) Species:
83333
(Escherichia coli K-12) [
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ISIKTPEDIEKMRVAGRLAAEVLEMIEPYVKPGVSTGELDRICNDYIVNE
QHAVSACLGYHGYPKSVCISINEVVCHGIPDDAKLLKDGDIVNIDVTVIK
DGFHGDTSKMFIVGKPTIMGERLCRITQESLYLALRMVKPGINLREIGAA
IQKFVEAEGFSVVREYCGHGIGRGFHEEPQVLHYDSRETNVVLKPGMTFT
IEPMVNAGKKEIRTMKDGWTVKTKDRSLSAQYEHTIVVTDNGCEILTLRK
DDTIPAIISHDE
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
2gg0 Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
2gg0
Serendipitous discovery of novel bacterial methionine aminopeptidase inhibitors.
Resolution
1.28 Å
Binding residue
(original residue number in PDB)
D97 D108 E235
Binding residue
(residue number reindexed from 1)
D95 D106 E233
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
H79 D97 D108 H171 R175 H178 Q182 E204 N208 Q233 E235
Catalytic site (residue number reindexed from 1)
H77 D95 D106 H169 R173 H176 Q180 E202 N206 Q231 E233
Enzyme Commision number
3.4.11.18
: methionyl aminopeptidase.
Gene Ontology
Molecular Function
GO:0004177
aminopeptidase activity
GO:0004239
initiator methionyl aminopeptidase activity
GO:0008198
ferrous iron binding
GO:0008235
metalloexopeptidase activity
GO:0046872
metal ion binding
GO:0046914
transition metal ion binding
GO:0070006
metalloaminopeptidase activity
Biological Process
GO:0006508
proteolysis
Cellular Component
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:2gg0
,
PDBe:2gg0
,
PDBj:2gg0
PDBsum
2gg0
PubMed
17120228
UniProt
P0AE18
|MAP1_ECOLI Methionine aminopeptidase (Gene Name=map)
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