Structure of PDB 1fkq Chain A Binding Site BS01
Receptor Information
>1fkq Chain A (length=124) Species:
9925
(Capra hircus) [
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MEQLTKCEVFQKLKDLKDYGGVSLPEWVCVAFHTSGYDTQAIVQNNDSTE
YGLFQINNKIWCKDDQNPHSRNICNISCDKFLDDDLTDDIVCAKKILDKV
GINYWLAHKALCSEKLDQWLCEKL
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1fkq Chain A Residue 124 [
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Receptor-Ligand Complex Structure
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PDB
1fkq
Contribution of Thr29 to the thermodynamic stability of goat alpha-lactalbumin as determined by experimental and theoretical approaches.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
K79 D82 D84 D87 D88
Binding residue
(residue number reindexed from 1)
K80 D83 D85 D88 D89
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T33 N45 S47 E49 N56
Catalytic site (residue number reindexed from 1)
T34 N46 S48 E50 N57
Enzyme Commision number
2.4.1.22
: lactose synthase.
Gene Ontology
Molecular Function
GO:0003796
lysozyme activity
GO:0004461
lactose synthase activity
GO:0005509
calcium ion binding
GO:0046872
metal ion binding
Biological Process
GO:0005989
lactose biosynthetic process
GO:0050829
defense response to Gram-negative bacterium
GO:0050830
defense response to Gram-positive bacterium
Cellular Component
GO:0005576
extracellular region
GO:0032991
protein-containing complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1fkq
,
PDBe:1fkq
,
PDBj:1fkq
PDBsum
1fkq
PubMed
11536356
UniProt
P00712
|LALBA_CAPHI Alpha-lactalbumin (Gene Name=LALBA)
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