Structure of PDB 2r5e Chain B Binding Site BS02
Receptor Information
>2r5e Chain B (length=419) Species:
7159
(Aedes aegypti) [
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NKFDLPKRYQGSTKSVWVEYIQLAAQYKPLNLGQGFPDYHAPKYALNALA
AAANSPDPLANQYTRGFGHPRLVQALSKLYSQLVDRTINPMTEVLVTVGA
YEALYATIQGHVDEGDEVIIIEPFFDCYEPMVKAAGGIPRFIPLKPNKTG
GTISSADWVLDNNELEALFNEKTKMIIINTPHNPLGKVMDRAELEVVANL
CKKWNVLCVSDEVYEHMVFEPFEHIRICTLPGMWERTITIGSAGKTFSLT
GWKIGWAYGPEALLKNLQMVHQNCVYTCATPIQEAIAVGFETELKRLKSP
ECYFNSISGELMAKRDYMASFLAEVGMNPTVPQGGYFMVADWSSLDSKVD
LTQETDARKDYRFTKWMTKSVGLQGIPPSAFYSEPNKHLGEDFVRYCFFK
KDENLQKAAEILRKWKGSS
Ligand information
Ligand ID
QLP
InChI
InChI=1S/C13H20N3O8P/c1-7-12(18)9(8(4-15-7)6-24-25(21,22)23)5-16-10(13(19)20)2-3-11(14)17/h4,10,16,18H,2-3,5-6H2,1H3,(H2,14,17)(H,19,20)(H2,21,22,23)/t10-/m0/s1
InChIKey
TUUVENFNODJVKV-JTQLQIEISA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(CN[C@@H](CCC(N)=O)C(O)=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)CN[C@@H](CCC(=O)N)C(=O)O)O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)CNC(CCC(=O)N)C(=O)O)O
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(CN[CH](CCC(N)=O)C(O)=O)c1O
ACDLabs 10.04
O=C(O)C(NCc1c(cnc(c1O)C)COP(=O)(O)O)CCC(=O)N
Formula
C13 H20 N3 O8 P
Name
N~2~-({3-HYDROXY-2-METHYL-5-[(PHOSPHONOOXY)METHYL]PYRIDIN-4-YL}METHYL)-L-GLUTAMINE;
N-({3-HYDROXY-2-METHYL-5-[(PHOSPHONOOXY)METHYL]PYRIDIN-4-YL}METHYL)-L-GLUTAMINE
ChEMBL
DrugBank
ZINC
ZINC000016052507
PDB chain
2r5e Chain B Residue 430 [
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Receptor-Ligand Complex Structure
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PDB
2r5e
Structural insight into the mechanism of substrate specificity of aedes kynurenine aminotransferase.
Resolution
1.84 Å
Binding residue
(original residue number in PDB)
W27 Q44 G109 A110 Y111 F135 N189 N193 D221 Y224 S252 K255 K263 F347 R405
Binding residue
(residue number reindexed from 1)
W17 Q34 G99 A100 Y101 F125 N179 N183 D211 Y214 S242 K245 K253 F337 R395
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F135 D221 V223 K255
Catalytic site (residue number reindexed from 1)
F125 D211 V213 K245
Enzyme Commision number
2.6.1.-
2.6.1.63
: kynurenine--glyoxylate transaminase.
2.6.1.7
: kynurenine--oxoglutarate transaminase.
Gene Ontology
Molecular Function
GO:0008483
transaminase activity
GO:0016212
kynurenine-oxoglutarate transaminase activity
GO:0030170
pyridoxal phosphate binding
GO:0047315
kynurenine-glyoxylate transaminase activity
Biological Process
GO:0009058
biosynthetic process
GO:0097053
L-kynurenine catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2r5e
,
PDBe:2r5e
,
PDBj:2r5e
PDBsum
2r5e
PubMed
18186649
UniProt
Q17CS8
|KAT_AEDAE Kynurenine aminotransferase (Gene Name=KAT)
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