Structure of PDB 4y50 Chain A Binding Site BS01
Receptor Information
>4y50 Chain A (length=330) Species:
5116
(Cryphonectria parasitica) [
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STGSATTTPIDSLDDAYITPVQIGTPAQTLNLDFDTGSSDLWVFSSETTA
SEVDGQTIYTPSKSTTAKLLSGATWSISYGDGSSSSGDVYTDTVSVGGLT
VTGQAVESAKKVSSSFTEDSTIDGLLGLAFSTLNTVSPTQQKTFFDNAKA
SLDSPVFTADLGYHAPGTYNFGFIDTTAYTGSITYTAVSTKQGFWEWTST
GYAVGSGTFKSTSIDGIADTGTTLLYLPATVVSAYWAQVSGAKSSSSVGG
YVFPCSATLPSFTFGVGSARIVIPGDYIDFGPISTGSSSCFGGIQSSAGI
GINIFGDVALKAAFVVFNGATTPTLGFASK
Ligand information
Ligand ID
47S
InChI
InChI=1S/C9H13N3O/c1-12(2)8-5-3-4-7(6-8)9(13)11-10/h3-6H,10H2,1-2H3,(H,11,13)
InChIKey
UBSSYVLPIDYZJC-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(c1cc(N(C)C)ccc1)NN
CACTVS 3.385
OpenEye OEToolkits 1.9.2
CN(C)c1cccc(c1)C(=O)NN
Formula
C9 H13 N3 O
Name
3-(dimethylamino)benzohydrazide
ChEMBL
DrugBank
ZINC
ZINC000002561227
PDB chain
4y50 Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4y50
A small nonrule of 3 compatible fragment library provides high hit rate of endothiapepsin crystal structures with various fragment chemotypes.
Resolution
1.32 Å
Binding residue
(original residue number in PDB)
D35 G80 I217 D219
Binding residue
(residue number reindexed from 1)
D35 G80 I217 D219
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D35 S38 D40 W42 Y79 D219 T222
Catalytic site (residue number reindexed from 1)
D35 S38 D40 W42 Y79 D219 T222
Enzyme Commision number
3.4.23.22
: endothiapepsin.
Gene Ontology
Molecular Function
GO:0004190
aspartic-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:4y50
,
PDBe:4y50
,
PDBj:4y50
PDBsum
4y50
PubMed
UniProt
P11838
|CARP_CRYPA Endothiapepsin (Gene Name=EAPA)
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