Structure of PDB 5lyx Chain A Binding Site BS03
Receptor Information
>5lyx Chain A (length=363) Species:
9606
(Homo sapiens) [
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KVQTDPPSVPICDLYPNGVFPKGQECEYPPTQDGRTAAWRTTSKKALDQA
SEEIWNDFREAAEAHRQVRKYVMSWIKPGMTMIEICEKLEDCSRKLIKEN
GLNAGLAFPTGCSLNNCAAHYTPNAGDTTVLQYDDICKIDFGTHISGRII
DCAFTVTFNPKYDTLLKAVKDATNTGIKCAGIDVRLCDVGEAIQEVMESY
EVEIDGKTYQVKPIRNLNGHSIGQYRIHAGKTVPIVKGGEATRMEEGEVY
AIETFGSTGKGVVHDDMECSHYMKNFDVGHVPIRLPRTKHLLNVINENFG
TLAFCRRWLDRLGESKYLMALKNLCDLGIVDPYPPLCDIKGSYTAQFEHT
ILLRPTCKEVVSR
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
5lyx Chain A Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
5lyx
Novel reversible methionine aminopeptidase-2 (MetAP-2) inhibitors based on purine and related bicyclic templates.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
D251 D262 E459
Binding residue
(residue number reindexed from 1)
D140 D151 E348
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D251 D262 H331 H339 E364 E459
Catalytic site (residue number reindexed from 1)
D140 D151 H220 H228 E253 E348
Enzyme Commision number
3.4.11.18
: methionyl aminopeptidase.
Gene Ontology
Molecular Function
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:5lyx
,
PDBe:5lyx
,
PDBj:5lyx
PDBsum
5lyx
PubMed
27998678
UniProt
P50579
|MAP2_HUMAN Methionine aminopeptidase 2 (Gene Name=METAP2)
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