Structure of PDB 2x93 Chain A Binding Site BS02
Receptor Information
>2x93 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
X93
InChI
InChI=1S/C22H30N2O5/c1-14(23-17(21(26)27)12-11-15-7-3-2-4-8-15)20(25)24-18-10-6-5-9-16(18)13-19(24)22(28)29/h2-4,7-8,14,16-19,23H,5-6,9-13H2,1H3,(H,26,27)(H,28,29)/t14-,16+,17-,18-,19-/m0/s1
InChIKey
AHYHTSYNOHNUSH-HXFGRODQSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CC(C(=O)N1C2CCCCC2CC1C(=O)O)NC(CCc3ccccc3)C(=O)O
CACTVS 3.385
C[CH](N[CH](CCc1ccccc1)C(O)=O)C(=O)N2[CH]3CCCC[CH]3C[CH]2C(O)=O
CACTVS 3.385
C[C@H](N[C@@H](CCc1ccccc1)C(O)=O)C(=O)N2[C@H]3CCCC[C@@H]3C[C@H]2C(O)=O
ACDLabs 10.04
O=C(O)C(NC(C(=O)N1C(C(=O)O)CC2CCCCC12)C)CCc3ccccc3
OpenEye OEToolkits 1.7.6
C[C@@H](C(=O)N1[C@H]2CCCC[C@@H]2C[C@H]1C(=O)O)N[C@@H](CCc3ccccc3)C(=O)O
Formula
C22 H30 N2 O5
Name
TRANDOLAPRILAT
ChEMBL
CHEMBL1201387
DrugBank
DB14209
ZINC
ZINC000003784432
PDB chain
2x93 Chain A Residue 1623 [
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Receptor-Ligand Complex Structure
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PDB
2x93
High Resolution Crystal Structures of Drosophila Melanogaster Angiotensin Converting Enzyme in Complex with Novel Inhibitors and Anti- Hypertensive Drugs.
Resolution
1.98 Å
Binding residue
(original residue number in PDB)
Q265 H337 A338 H367 E368 E395 K495 H497 V502 Y504 Y507
Binding residue
(residue number reindexed from 1)
Q249 H321 A322 H351 E352 E379 K479 H481 V486 Y488 Y491
Annotation score
1
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:2x93
,
PDBe:2x93
,
PDBj:2x93
PDBsum
2x93
PubMed
20488190
UniProt
Q10714
|ACE_DROME Angiotensin-converting enzyme (Gene Name=Ance)
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