Structure of PDB 7a14 Chain A Binding Site BS01
Receptor Information
>7a14 Chain A (length=366) Species:
9606
(Homo sapiens) [
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KVQTDPPSVPICDLYPNGVFPKGQECEYPPTQDGRTAAWRTTSEEKKALD
QASEEIWNDFREAAEAHRQVRKYVMSWIKPGMTMIEICEKLEDCSRKLIK
ENGLNAGLAFPTGCSLNNCAAHYTPNAGDTTVLQYDDICKIDFGTHISGR
IIDCAFTVTFNPKYDTLLKAVKDATNTGIKCAGIDVRLCDVGEAIQEVME
SYEVEIDGKTYQVKPIRNLNGHSIGQYRIHAGKTVPIVKATRMEEGEVYA
IETFGSTGKGVVHDDMECSHYMKNFDVGHVPIRLPRTKHLLNVINENFGT
LAFCRRWLDRLGESKYLMALKNLCDLGIVDPYPPLCDIKGSYTAQFEHTI
LLRPTCKEVVSRGDDY
Ligand information
Ligand ID
QVB
InChI
InChI=1S/C18H16ClFN2O2/c1-9(2)24-15-6-4-3-5-10(15)16-11-7-12(19)13(20)8-14(11)22-17(16)18(21)23/h3-9,22H,1-2H3,(H2,21,23)
InChIKey
CNUHFUPIGPUPON-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
CC(C)Oc1ccccc1c2c3cc(c(cc3[nH]c2C(=O)N)F)Cl
CACTVS 3.385
CC(C)Oc1ccccc1c2c([nH]c3cc(F)c(Cl)cc23)C(N)=O
Formula
C18 H16 Cl F N2 O2
Name
5-chloranyl-6-fluoranyl-3-(2-propan-2-yloxyphenyl)-1~{H}-indole-2-carboxamide
ChEMBL
CHEMBL4796852
DrugBank
ZINC
PDB chain
7a14 Chain A Residue 508 [
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Receptor-Ligand Complex Structure
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PDB
7a14
Structure-based optimisation of orally active & reversible MetAP-2 inhibitors maintaining a tight 'molecular budget'.
Resolution
2.14 Å
Binding residue
(original residue number in PDB)
F219 H231 H331 I338 H339 Y383 A414 Y444 L447
Binding residue
(residue number reindexed from 1)
F110 H122 H222 I229 H230 Y271 A302 Y332 L335
Annotation score
1
Binding affinity
MOAD
: ic50=0.00000001M
Enzymatic activity
Catalytic site (original residue number in PDB)
D251 D262 H331 H339 E364 E459
Catalytic site (residue number reindexed from 1)
D142 D153 H222 H230 E252 E347
Enzyme Commision number
3.4.11.18
: methionyl aminopeptidase.
Gene Ontology
Molecular Function
GO:0070006
metalloaminopeptidase activity
Biological Process
GO:0006508
proteolysis
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:7a14
,
PDBe:7a14
,
PDBj:7a14
PDBsum
7a14
PubMed
32919012
UniProt
P50579
|MAP2_HUMAN Methionine aminopeptidase 2 (Gene Name=METAP2)
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