Structure of PDB 1ent Chain E Binding Site BS01
Receptor Information
>1ent Chain E (length=330) Species:
5116
(Cryphonectria parasitica) [
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STGSATTTPIDSLDDAYITPVQIGTPAQTLNLDFDTGSSDLWVFSSETTA
SEVDGQTIYTPSKSTTAKLLSGATWSISYGDGSSSSGDVYTDTVSVGGLT
VTGQAVESAKKVSSSFTEDSTIDGLLGLAFSTLNTVSPTQQKTFFDNAKA
SLDSPVFTADLGYHAPGTYNFGFIDTTAYTGSITYTAVSTKQGFWEWTST
GYAVGSGTFKSTSIDGIADTGTTLLYLPATVVSAYWAQVSGAKSSSSVGG
YVFPCSATLPSFTFGVGSARIVIPGDYIDFGPISTGSSSCFGGIQSSAGI
GINIFGDVALKAAFVVFNGATTPTLGFASK
Ligand information
Ligand ID
0EM
InChI
InChI=1S/C32H51N6O7P/c1-8-22(4)17-34-27(39)19-46(43,44)28(14-21(2)3)38-30(41)26(16-24-18-33-20-35-24)36-29(40)25(15-23-12-10-9-11-13-23)37-31(42)45-32(5,6)7/h9-13,18,20-22,25-26,28H,8,14-17,19H2,1-7H3,(H,33,35)(H,34,39)(H,36,40)(H,37,42)(H,38,41)(H,43,44)/p+1/t22-,25-,26-,28+/m0/s1
InChIKey
ZQDBBPUTYSTPQE-DYYCDWSUSA-O
SMILES
Software
SMILES
CACTVS 3.341
CC[CH](C)CNC(=O)C[P](O)(=O)[CH](CC(C)C)NC(=O)[CH](Cc1c[nH]c[nH+]1)NC(=O)[CH](Cc2ccccc2)NC(=O)OC(C)(C)C
CACTVS 3.341
CC[C@H](C)CNC(=O)C[P@](O)(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c[nH+]1)NC(=O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C
ACDLabs 10.04
O=C(NCC(C)CC)CP(=O)(O)C(NC(=O)C(NC(=O)C(NC(=O)OC(C)(C)C)Cc1ccccc1)Cc2cnc[nH+]2)CC(C)C
Formula
C32 H52 N6 O7 P
Name
N-(tert-butoxycarbonyl)-L-phenylalanyl-N-{(1S)-1-[(R)-hydroxy(2-{[(2S)-2-methylbutyl]amino}-2-oxoethyl)phosphoryl]-3-methylbutyl}-3-(1H-imidazol-3-ium-4-yl)-L-alaninamide;
PD-130,328
ChEMBL
DrugBank
ZINC
PDB chain
1ent Chain E Residue 822 [
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Receptor-Ligand Complex Structure
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PDB
1ent
X-ray analyses of aspartic proteinases. The three-dimensional structure at 2.1 A resolution of endothiapepsin.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
D12 D32 Y75 G76 D77 F189 D215 G217 T218 T219 I297
Binding residue
(residue number reindexed from 1)
D15 D35 Y79 G80 D81 F194 D219 G221 T222 T223 I300
Annotation score
1
Binding affinity
MOAD
: Ki=110nM
PDBbind-CN
: -logKd/Ki=6.96,Ki=110nM
Enzymatic activity
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:1ent
,
PDBe:1ent
,
PDBj:1ent
PDBsum
1ent
PubMed
2179568
UniProt
P11838
|CARP_CRYPA Endothiapepsin (Gene Name=EAPA)
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