Literature summary extracted from
Wu, F.; Yu, J.; Gehring, H.
Inhibitory and structural studies of novel coenzyme-substrate analogs of human histidine decarboxylase (2007), FASEB J., 22, 890-897.
Activating Compound
EC Number |
Activating Compound |
Comment |
Organism |
Structure |
---|
4.1.1.22 |
additional information |
12-O-tetradecanoylphorbol-13-acetate induces the enzyme |
Homo sapiens |
|
Application
EC Number |
Application |
Comment |
Organism |
---|
4.1.1.22 |
drug development |
HDC is a potential target to attenuate histamine production in certain pathological states using structure-based inhibitors, design, synthesis, and test of potentially membrane-permeable pyridoxyl-substrate conjugates as inhibitors for human HDC and modeling of an active site for hHDC, which is compatible with the experimental data, overview |
Homo sapiens |
Inhibitors
EC Number |
Inhibitors |
Comment |
Organism |
Structure |
---|
4.1.1.22 |
additional information |
design, synthesis, and test of potentially membrane-permeable pyridoxyl-substrate conjugates as inhibitors for human HDC and modeling of an active site for hHDC, which is compatible with the experimental data, structure-activity relationship, overview |
Homo sapiens |
|
4.1.1.22 |
pyridoxyl-histidine methyl ester conjugate |
structure-based inhibitor, binding structure |
Homo sapiens |
|
Natural Substrates/ Products (Substrates)
EC Number |
Natural Substrates |
Organism |
Comment (Nat. Sub.) |
Natural Products |
Comment (Nat. Pro.) |
Rev. |
Reac. |
---|
4.1.1.22 |
L-histidine |
Homo sapiens |
- |
histamine + CO2 |
- |
? |
|
Organism
EC Number |
Organism |
UniProt |
Comment |
Textmining |
---|
4.1.1.22 |
Homo sapiens |
P19113 |
- |
- |
Reaction
EC Number |
Reaction |
Comment |
Organism |
Reaction ID |
---|
4.1.1.22 |
L-histidine = histamine + CO2 |
structure-activity relationship, active site structure, molecular modeling, the imidazole ring is located in a pocket composed of residues Tyr-81B, Asn-302B, Ser-304B, Lys-305B, Leu-102A, Phe-104A, and Ser-354A |
Homo sapiens |
|
Source Tissue
EC Number |
Source Tissue |
Comment |
Organism |
Textmining |
---|
4.1.1.22 |
HMC-1 cell |
- |
Homo sapiens |
- |
Substrates and Products (Substrate)
EC Number |
Substrates |
Comment Substrates |
Organism |
Products |
Comment (Products) |
Rev. |
Reac. |
---|
4.1.1.22 |
L-histidine |
- |
Homo sapiens |
histamine + CO2 |
- |
? |
|
4.1.1.22 |
L-histidine |
the binding site of HDC does not tolerate groups other than the imidazole side chain of histidine |
Homo sapiens |
histamine + CO2 |
- |
? |
|
Subunits
EC Number |
Subunits |
Comment |
Organism |
---|
4.1.1.22 |
More |
structure molecular modeling |
Homo sapiens |
Synonyms
EC Number |
Synonyms |
Comment |
Organism |
---|
4.1.1.22 |
HDC |
- |
Homo sapiens |
Temperature Optimum [°C]
EC Number |
Temperature Optimum [°C] |
Temperature Optimum Maximum [°C] |
Comment |
Organism |
---|
4.1.1.22 |
37 |
- |
assay at |
Homo sapiens |
pH Optimum
EC Number |
pH Optimum Minimum |
pH Optimum Maximum |
Comment |
Organism |
---|
4.1.1.22 |
6.8 |
- |
assay at |
Homo sapiens |
Cofactor
EC Number |
Cofactor |
Comment |
Organism |
Structure |
---|
4.1.1.22 |
pyridoxal 5'-phosphate |
dependent on |
Homo sapiens |
|