Structure of PDB 7q28 Chain A Binding Site BS02
Receptor Information
>7q28 Chain A (length=578) Species:
9606
(Homo sapiens) [
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DEAEASKFVEEYDRTSQVVWNEYAGANWNYNTNITTETSKILLQKNMQIA
QHTLKYGTQARKFDVNQLQNTTIKRIIKKVQDLERAALPAQELEEYNKIL
LDMETTYSVATVCHPQGSCLQLEPDLTNVMATSRKYEDLLWAWEGWRDKA
GRAILQFYPKYVELINQAARLNGYVDAGDSWRSMYETPSLEQDLERLFQE
LQPLYLNLHAYVRRALHRHYGAQHINLEGPIPAHLLGNMWAQTWSNIYDL
VVPFPSAPSMDTTEAMLKQGWTPRRMFKEADDFFTSLGLLPVPPEFWQKS
MLEKPTDGREVVCHASAWDFYNGKDFRIKQCTTVNLEDLVVAHHEMGHIQ
YFMQYKDLPVALREGANPGFHEAIGDVLALSVSTPKHLHSLNLLSSEGGS
DEHDINFLMKMALDKIAFIPFSYLVDQWRWRVFDGSITKENYNQEWWSLR
LKYQGLCPPVPRTQGDFDPGAKFHIPSSVPYIRYFVSFIIQFQFHEALCQ
AAGHTGPLHKCDIYQSKEAGQRLATAMKLGFSRPWPEAMQLITGQPQMSA
SAMLSYFKPLLDWLRTENELHGEKLGWP
Ligand information
Ligand ID
8J9
InChI
InChI=1S/C25H32N2O6/c1-2-3-9-20(26-21(24(30)31)15-12-17-7-5-4-6-8-17)23(29)27-22(25(32)33)16-18-10-13-19(28)14-11-18/h4-8,10-11,13-14,20-22,26,28H,2-3,9,12,15-16H2,1H3,(H,27,29)(H,30,31)(H,32,33)/t20-,21-,22-/m0/s1
InChIKey
QJZUXIPDHISQFZ-FKBYEOEOSA-N
SMILES
Software
SMILES
CACTVS 3.385
CCCC[C@H](N[C@@H](CCc1ccccc1)C(O)=O)C(=O)N[C@@H](Cc2ccc(O)cc2)C(O)=O
OpenEye OEToolkits 2.0.7
CCCC[C@@H](C(=O)N[C@@H](Cc1ccc(cc1)O)C(=O)O)N[C@@H](CCc2ccccc2)C(=O)O
OpenEye OEToolkits 2.0.7
CCCCC(C(=O)NC(Cc1ccc(cc1)O)C(=O)O)NC(CCc2ccccc2)C(=O)O
CACTVS 3.385
CCCC[CH](N[CH](CCc1ccccc1)C(O)=O)C(=O)N[CH](Cc2ccc(O)cc2)C(O)=O
Formula
C25 H32 N2 O6
Name
(2~{S})-2-[[(2~{S})-1-[[(2~{S})-3-(4-hydroxyphenyl)-1-oxidanyl-1-oxidanylidene-propan-2-yl]amino]-1-oxidanylidene-hexan-2-yl]amino]-4-phenyl-butanoic acid
ChEMBL
CHEMBL5077796
DrugBank
ZINC
PDB chain
7q28 Chain A Residue 703 [
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Receptor-Ligand Complex Structure
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PDB
7q28
Probing the Requirements for Dual Angiotensin-Converting Enzyme C-Domain Selective/Neprilysin Inhibition.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
Q281 H353 A354 H383 E384 H387 E411 K511 H513 V518 Y520 Y523 F527
Binding residue
(residue number reindexed from 1)
Q242 H314 A315 H344 E345 H348 E372 K472 H474 V479 Y481 Y484 F488
Annotation score
2
Enzymatic activity
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7q28
,
PDBe:7q28
,
PDBj:7q28
PDBsum
7q28
PubMed
35113565
UniProt
P12821
|ACE_HUMAN Angiotensin-converting enzyme (Gene Name=ACE)
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