Structure of PDB 2x97 Chain A Binding Site BS01
Receptor Information
>2x97 Chain A (length=598) Species:
7227
(Drosophila melanogaster) [
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ALVKEEIQAKEYLENLNKELAKRTNVETEAAWAYGSNITDENEKKKNEIS
AELAKFMKEVASDTTKFQWRSYQSEDLKRQFKALTKLGYAALPEDDYAEL
LDTLSAMESNFAKVKVCDYKDSTKCDLALDPEIEEVISKSRDHEELAYYW
REFYDKAGTAVRSQFERYVELNTKAAKLNNFTSGAEAWLDEYEDDTFEQQ
LEDIFADIRPLYQQIHGYVRFRLRKHYGDAVVSETGPIPMHLLGNMWAQQ
WSEIADIVSPFPEKPLVDVSAEMEKQGYTPLKMFQMGDDFFTSMNLTKLP
QDFWDKSIIEKPTDGRDLVCHASAWDFYLTDDVRIKQCTRVTQDQLFTVH
HELGHIQYFLQYQHQPFVYRTGANPGFHEAVGDVLSLSVSTPKHLEKIGL
LKDYVRDDEARINQLFLTALDKIVFLPFAFTMDKYRWSLFRGEVDKANWN
CAFWKLRDEYSGIEPPVVRSEKDFDAPAKYHISADVEYLRYLVSFIIQFQ
FYKSACIKAGQYDPDNVELPLDNCDIYGSAAAGAAFHNMLSMGASKPWPD
ALEAFNGERIMSGKAIAEYFEPLRVWLEAENIKNNVHIGWTTSNKCVS
Ligand information
Ligand ID
RX4
InChI
InChI=1S/C21H31N4O8P/c1-12(20(30)23-13(2)19(22)29)11-34(32,33)17(9-15-7-5-4-6-8-15)25-21(31)16(10-18(27)28)24-14(3)26/h4-8,12-13,16-17H,9-11H2,1-3H3,(H2,22,29)(H,23,30)(H,24,26)(H,25,31)(H,27,28)(H,32,33)/t12-,13+,16+,17-/m1/s1
InChIKey
OCAZUTUOYLAIOA-OSRSDYAFSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
CC(CP(=O)(C(Cc1ccccc1)NC(=O)C(CC(=O)O)NC(=O)C)O)C(=O)NC(C)C(=O)N
ACDLabs 12.01
O=C(N)C(NC(=O)C(C)CP(=O)(O)C(NC(=O)C(NC(=O)C)CC(=O)O)Cc1ccccc1)C
CACTVS 3.370
C[C@H](C[P](O)(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(C)=O)C(=O)N[C@@H](C)C(N)=O
OpenEye OEToolkits 1.7.0
C[C@H](C[P@@](=O)([C@H](Cc1ccccc1)NC(=O)[C@H](CC(=O)O)NC(=O)C)O)C(=O)N[C@@H](C)C(=O)N
CACTVS 3.370
C[CH](C[P](O)(=O)[CH](Cc1ccccc1)NC(=O)[CH](CC(O)=O)NC(C)=O)C(=O)N[CH](C)C(N)=O
Formula
C21 H31 N4 O8 P
Name
N~2~-acetyl-N-{(1R)-1-[(S)-[(2S)-3-{[(2S)-1-amino-1-oxopropan-2-yl]amino}-2-methyl-3-oxopropyl](hydroxy)phosphoryl]-2-phenylethyl}-L-alpha-asparagine;
Ac-Asp-(L)Phe(PO2CH2)(L)Ala-Ala-NH2;
RXP407
ChEMBL
CHEMBL1235767
DrugBank
ZINC
ZINC000013915097
PDB chain
2x97 Chain A Residue 1615 [
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Receptor-Ligand Complex Structure
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PDB
2x97
High Resolution Crystal Structures of Drosophila Melanogaster Angiotensin Converting Enzyme in Complex with Novel Inhibitors and Anti- Hypertensive Drugs.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
Q265 H337 A338 S339 A340 H367 E368 H371 F375 E395 F441 K495 Y496 H497 V502 Y504 Y507
Binding residue
(residue number reindexed from 1)
Q249 H321 A322 S323 A324 H351 E352 H355 F359 E379 F425 K479 Y480 H481 V486 Y488 Y491
Annotation score
1
Binding affinity
MOAD
: Ki=2200nM
PDBbind-CN
: -logKd/Ki=5.66,Ki=2200nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H337 A338 H367 E368 H371 E395 H497 Y507
Catalytic site (residue number reindexed from 1)
H321 A322 H351 E352 H355 E379 H481 Y491
Enzyme Commision number
3.4.15.1
: peptidyl-dipeptidase A.
Gene Ontology
Molecular Function
GO:0008237
metallopeptidase activity
GO:0008241
peptidyl-dipeptidase activity
Biological Process
GO:0006508
proteolysis
Cellular Component
GO:0016020
membrane
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2x97
,
PDBe:2x97
,
PDBj:2x97
PDBsum
2x97
PubMed
20488190
UniProt
Q10714
|ACE_DROME Angiotensin-converting enzyme (Gene Name=Ance)
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