Structure of PDB 5yn3 Chain A Binding Site BS02
Receptor Information
>5yn3 Chain A (length=435) Species:
73868
(Piromyces sp. E2) [
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KEYFPQIQKIKFEGKDSKNPLAFHYYDAEKEVMGKKMKDWLRFAMAWWHT
LCAEGADQFGGGTKSFPWNEGTDAIEIAKQKVDAGFEIMQKLGIPYYCFH
DVDLVSEGNSIEEYESNLKAVVAYLKEKQKETGIKLLWSTANVFGHKRYM
NGASTNPDFDVVARAIVQIKNAIDAGIELGAENYVFWGGREGYMSLLNTD
QKREKEHMATMLTMARDYARSKGFKGTFLIEPKPMEPTKHQYDVDTETAI
GFLKAHNLDKDFKVNIEVNHATLAGHTFEHELACAVDAGMLGSIDANRGD
YQNGWDTDQFPIDQYELVQAWMEIIRGGGFVTGGTNFDAKTRRNSTDLED
IIIAHVSGMDAMARALENAAKLLQESPYTKMKKERYASFDSGIGKDFEDG
KLTLEQVYEYGKKNGEPKQTSGKQELYEAIVAMYQ
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
5yn3 Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5yn3
Crystal Structure and Biochemical Characterization of Xylose Isomerase fromPiromycessp. E2.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
E269 H272 D308 D310
Binding residue
(residue number reindexed from 1)
E267 H270 D306 D308
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H102 D105 W140 E233 K235 E269 H272 D297 D308 D310 D340
Catalytic site (residue number reindexed from 1)
H100 D103 W138 E231 K233 E267 H270 D295 D306 D308 D338
Enzyme Commision number
5.3.1.5
: xylose isomerase.
Gene Ontology
Molecular Function
GO:0009045
xylose isomerase activity
GO:0016853
isomerase activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0042732
D-xylose metabolic process
GO:0044577
D-xylose catabolic process to ethanol
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Molecular Function
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Biological Process
External links
PDB
RCSB:5yn3
,
PDBe:5yn3
,
PDBj:5yn3
PDBsum
5yn3
PubMed
29385668
UniProt
Q9P8C9
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