Structure of PDB 3kcl Chain A Binding Site BS01
Receptor Information
>3kcl Chain A (length=388) Species:
1929
(Streptomyces rubiginosus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MNYQPTPEDRFTFGLWTVGWQGRDPFGDATRRALDPVESVRRLAELGAHG
VTFHDDDLIPFGSSDSEREEHVKRFRQALDDTGMKVPMATTNLFTHPVFK
DGGFTANDRDVRRYALRKTIRNIDLAVELGAETYVAWGGREGAESGGAKD
VRDALDRMKEAFDLLGEYVTSQGYDIRFAIEPKPNEPRGDILLPTVGHAL
AFIERLERPELYGVNPEVGHEQMAGLNFPHGIAQALWAGKLFHIDLNGQN
GIKYDQDLRFGAGDLRAAFWLVDLLESAGYSGPRHFDFKPPRTEDFDGVW
ASAAGCMRNYLILKERAAAFRADPEVQEALRASRLDELARPTAADGLQAL
LDDRSAFEEFDVDAAAARGMAFERLDQLAMDHLLGARG
Ligand information
Ligand ID
CD
InChI
InChI=1S/Cd/q+2
InChIKey
WLZRMCYVCSSEQC-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Cd++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cd+2]
Formula
Cd
Name
CADMIUM ION
ChEMBL
DrugBank
ZINC
PDB chain
3kcl Chain A Residue 391 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
3kcl
Metal ion roles and the movement of hydrogen during reaction catalyzed by D-xylose isomerase: a joint x-ray and neutron diffraction study.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
E217 H220 D255 D257
Binding residue
(residue number reindexed from 1)
E217 H220 D255 D257
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:0042732
D-xylose metabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3kcl
,
PDBe:3kcl
,
PDBj:3kcl
PDBsum
3kcl
PubMed
20541506
UniProt
P24300
|XYLA_STRRU Xylose isomerase (Gene Name=xylA)
[
Back to BioLiP
]