Structure of PDB 2esf Chain B Binding Site BS02
Receptor Information
>2esf Chain B (length=214) Species:
562
(Escherichia coli) [
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KDIDTLISNNALWSKMLVEEDPGFFEKLAQAQKPRFLWIGCSDSRVPAER
LTGLEPGELFVHRNVANLVIHTDLNCLSVVQYAVDVLEVEHIIICGHYGC
GGVQAAVENPELGLINNWLLHIRDIWFKHSSLLGEMPQERRLDTLCELNV
MEQVYNLGHSTIMQSAWKRGQKVTIHGWAYGIHDGLLRDLDVTATNRETL
EQRYRHGISNLKLK
Ligand information
Ligand ID
BCT
InChI
InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4)/p-1
InChIKey
BVKZGUZCCUSVTD-UHFFFAOYSA-M
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)(O)[O-]
CACTVS 3.341
OC([O-])=O
ACDLabs 10.04
[O-]C(=O)O
Formula
C H O3
Name
BICARBONATE ION
ChEMBL
DrugBank
ZINC
PDB chain
2esf Chain B Residue 2498 [
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Receptor-Ligand Complex Structure
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PDB
2esf
Identification of a Novel Noncatalytic Bicarbonate Binding Site in Eubacterial beta-Carbonic Anhydrase.
Resolution
2.25 Å
Binding residue
(original residue number in PDB)
W39 V47 R64 Y181
Binding residue
(residue number reindexed from 1)
W38 V46 R63 Y180
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
C42 D44 R46 H98 C101
Catalytic site (residue number reindexed from 1)
C41 D43 R45 H97 C100
Enzyme Commision number
4.2.1.1
: carbonic anhydrase.
Gene Ontology
Molecular Function
GO:0004089
carbonate dehydratase activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016829
lyase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0015976
carbon utilization
GO:0051289
protein homotetramerization
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2esf
,
PDBe:2esf
,
PDBj:2esf
PDBsum
2esf
PubMed
16584170
UniProt
P61517
|CAN_ECOLI Carbonic anhydrase 2 (Gene Name=can)
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