Structure of PDB 3do2 Chain A Binding Site BS07
Receptor Information
>3do2 Chain A (length=316) Species:
1427
(Bacillus thermoproteolyticus) [
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ITGTSTVGVGRGVLGDQKNINTTYSTYYYLQDNTRGNGIFTYDAKYRTTL
PGSLWADADNQFFASYDAPAVDAHYYAGVTYDYYKNVHNRLSYDGNNAAI
RSSVHYSQGYNNAFWNGSQMVYGDGDGQTFIPLSGGIDVVAHELTHAVTD
YTAGLIYQNESGAINEAISDIFGTLVEFYANKNPDWEIGEDVYTPGISGD
SLRSMSDPAKYGDPDHYSKRYTGTQDNGGVHINSGIINKAAYLISQGGTH
YGVSVVGIGRDKLGKIFYRALTQYLTPTSNFSQLRAAAVQSATDLYGSTS
QEVASVKQAFDAVGVK
Ligand information
Ligand ID
LYS
InChI
InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/p+1/t5-/m0/s1
InChIKey
KDXKERNSBIXSRK-YFKPBYRVSA-O
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCCC[NH3+])C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCCC[NH3+]
OpenEye OEToolkits 1.5.0
C(CC[NH3+])C[C@@H](C(=O)O)N
CACTVS 3.341
N[C@@H](CCCC[NH3+])C(O)=O
OpenEye OEToolkits 1.5.0
C(CC[NH3+])CC(C(=O)O)N
Formula
C6 H15 N2 O2
Name
LYSINE
ChEMBL
DrugBank
ZINC
PDB chain
3do2 Chain A Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
3do2
Radiation damage in protein structural characterization by Synchrotron Radiation: State of the art and Nanotechnology-based perspective
Resolution
1.22 Å
Binding residue
(original residue number in PDB)
N112 L202 H231
Binding residue
(residue number reindexed from 1)
N112 L202 H231
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H142 E143 H146 Y157 E166 D226 H231
Catalytic site (residue number reindexed from 1)
H142 E143 H146 Y157 E166 D226 H231
Enzyme Commision number
3.4.24.27
: thermolysin.
Gene Ontology
Molecular Function
GO:0004222
metalloendopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:3do2
,
PDBe:3do2
,
PDBj:3do2
PDBsum
3do2
PubMed
UniProt
P00800
|THER_BACTH Thermolysin (Gene Name=npr)
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