Structure of PDB 3kbv Chain A Binding Site BS02
Receptor Information
>3kbv Chain A (length=388) Species:
1929
(Streptomyces rubiginosus) [
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MNYQPTPEDRFTFGLWTVGWQGRDPFGDATRRALDPVESVRRLAELGAHG
VTFHDDDLIPFGSSDSEREEHVKRFRQALDDTGMKVPMATTNLFTHPVFK
DGGFTANDRDVRRYALRKTIRNIDLAVELGAETYVAWGGREGAESGGAKD
VRDALDRMKEAFDLLGEYVTSQGYDIRFAIEPKPNEPRGDILLPTVGHAL
AFIERLERPELYGVNPEVGHEQMAGLNFPHGIAQALWAGKLFHIDLNGQN
GIKYDQDLRFGAGDLRAAFWLVDLLESAGYSGPRHFDFKPPRTEDFDGVW
ASAAGCMRNYLILKERAAAFRADPEVQEALRASRLDELARPTAADGLQAL
LDDRSAFEEFDVDAAAARGMAFERLDQLAMDHLLGARG
Ligand information
Ligand ID
NI
InChI
InChI=1S/Ni/q+2
InChIKey
VEQPNABPJHWNSG-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ni++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ni+2]
Formula
Ni
Name
NICKEL (II) ION
ChEMBL
DrugBank
DB14204
ZINC
PDB chain
3kbv Chain A Residue 392 [
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Receptor-Ligand Complex Structure
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PDB
3kbv
Metal ion roles and the movement of hydrogen during reaction catalyzed by D-xylose isomerase: a joint x-ray and neutron diffraction study.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
E181 E217 D245 D287
Binding residue
(residue number reindexed from 1)
E181 E217 D245 D287
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H54 D57 M88 E181 K183 E217 H220 D245 D255 D257 D287
Catalytic site (residue number reindexed from 1)
H54 D57 M88 E181 K183 E217 H220 D245 D255 D257 D287
Enzyme Commision number
5.3.1.5
: xylose isomerase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0009045
xylose isomerase activity
GO:0016853
isomerase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0042732
D-xylose metabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3kbv
,
PDBe:3kbv
,
PDBj:3kbv
PDBsum
3kbv
PubMed
20541506
UniProt
P24300
|XYLA_STRRU Xylose isomerase (Gene Name=xylA)
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