Structure of PDB 1lnb Chain E Binding Site BS01
Receptor Information
>1lnb Chain E (length=316) Species:
1427
(Bacillus thermoproteolyticus) [
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ITGTSTVGVGRGVLGDQKNINTTYSTYYYLQDNTRGDGIFTYDAKYRTTL
PGSLWADADNQFFASYDAPAVDAHYYAGVTYDYYKNVHNRLSYDGNNAAI
RSSVHYSQGYNNAFWNGSEMVYGDGDGQTFIPLSGGIDVVAHELTHAVTD
YTAGLIYQNESGAINEAISDIFGTLVEFYANKNPDWEIGEDVYTPGISGD
SLRSMSDPAKYGDPDHYSKRYTGTQDNGGVHINSGIINKAAYLISQGGTH
YGVSVVGIGRDKLGKIFYRALTQYLTPTSNFSQLRAAAVQSATDLYGSTS
QEVASVKQAFDAVGVK
Ligand information
Ligand ID
VAL
InChI
InChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/t4-/m0/s1
InChIKey
KZSNJWFQEVHDMF-BYPYZUCNSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)C(N)C(C)C
OpenEye OEToolkits 1.5.0
CC(C)C(C(=O)O)N
OpenEye OEToolkits 1.5.0
CC(C)[C@@H](C(=O)O)N
CACTVS 3.341
CC(C)[C@H](N)C(O)=O
CACTVS 3.341
CC(C)[CH](N)C(O)=O
Formula
C5 H11 N O2
Name
VALINE
ChEMBL
CHEMBL43068
DrugBank
DB00161
ZINC
ZINC000000895099
PDB chain
1lnb Chain E Residue 1321 [
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Receptor-Ligand Complex Structure
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PDB
1lnb
Structural analysis of zinc substitutions in the active site of thermolysin.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
N112 E143 R203
Binding residue
(residue number reindexed from 1)
N112 E143 R203
Annotation score
4
Enzymatic activity
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:1lnb
,
PDBe:1lnb
,
PDBj:1lnb
PDBsum
1lnb
PubMed
8535232
UniProt
P00800
|THER_BACTH Thermolysin (Gene Name=npr)
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