Structure of PDB 2huf Chain A Binding Site BS02
Receptor Information
>2huf Chain A (length=385) Species:
7159
(Aedes aegypti) [
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MEYKVTPPAVLREPLVTPNKLLMGPGPSNAPQRVLDAMSRPILGHLHPET
LKIMDDIKEGVRYLFQTNNIATFCLSASGHGGMEATLCNLLEDGDVILIG
HTGHWGDRSADMATRYGADVRVVKSKVGQSLSLDEIRDALLIHKPSVLFL
TQGDSSTGVLQGLEGVGALCHQHNCLLIVDTVASLGGAPMFMDRWEIDAM
YTGSQKVLGAPPGITPVSFSHRAVERYKRRNTKVKVYYWDMSLVGDYWGC
FGRPRIYHHTISSTLLYGLREAIAMACEEGLPALIARHEDCAKRLYRGLQ
DAGFELYADPKDRLSTVTTIKVPQGVDWLKAAQYAMKTYLVEISGGLGPT
AGQVFRIGLMGQNATTERVDRVLQVFQEAVAAVKP
Ligand information
Ligand ID
1BO
InChI
InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3
InChIKey
LRHPLDYGYMQRHN-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OpenEye OEToolkits 1.5.0
CCCCO
ACDLabs 10.04
OCCCC
Formula
C4 H10 O
Name
1-BUTANOL;
BUTAN-1-OL
ChEMBL
CHEMBL14245
DrugBank
DB02145
ZINC
ZINC000001530354
PDB chain
2huf Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
2huf
Crystal Structures of Aedes aegypti Alanine Glyoxylate Aminotransferase.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
H45 Y257
Binding residue
(residue number reindexed from 1)
H45 Y257
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.6.1.44
: alanine--glyoxylate transaminase.
Gene Ontology
Molecular Function
GO:0004760
L-serine-pyruvate transaminase activity
GO:0008453
alanine-glyoxylate transaminase activity
GO:0008483
transaminase activity
GO:0016740
transferase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0009436
glyoxylate catabolic process
GO:0019265
glycine biosynthetic process, by transamination of glyoxylate
Cellular Component
GO:0005777
peroxisome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2huf
,
PDBe:2huf
,
PDBj:2huf
PDBsum
2huf
PubMed
16990263
UniProt
Q3LSM4
|AGT_AEDAE Alanine--glyoxylate aminotransferase (Gene Name=AGT)
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