Structure of PDB 1f2d Chain D Binding Site BS01
Receptor Information
>1f2d Chain D (length=341) [
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AGVAKFAKYPLTFGPSPISNLNRLSQHLGSKVNVYAKREDCNSGLAFGGN
KLRKLEYIVPDIVEGDYTHLVSIGGRQSNQTRMVAALAAKLGKKCVLIQE
DWVPIPEAEKDVYNRVGNIELSRIMGADVRVIEDGFDIGMRKSFANALQE
LEDAGHKPYPIPAGCSEHKYGGLGFVGFADEVINQEVELGIKFDKIVVCC
VTGSTTAGILAGMAQYGRQDDVIAIDASFTSEKTKEQTLRIANNTAKLIG
VEHEFKDFTLDTRFAYPCYGVPNEGTIEAIRTCAEQEGVLTDPVYEGKSM
QGLIALIKEDYFKPGANVLYVHLGGAPALSAYSSFFPTKTA
Ligand information
Ligand ID
PLP
InChI
InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14)
InChIKey
NGVDGCNFYWLIFO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(C=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)C=O)O
ACDLabs 10.04
O=P(O)(O)OCc1cnc(c(O)c1C=O)C
Formula
C8 H10 N O6 P
Name
PYRIDOXAL-5'-PHOSPHATE;
VITAMIN B6 Phosphate
ChEMBL
CHEMBL82202
DrugBank
DB00114
ZINC
ZINC000001532514
PDB chain
1f2d Chain D Residue 342 [
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Receptor-Ligand Complex Structure
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PDB
1f2d
Crystal structure of 1-aminocyclopropane-1-carboxylate deaminase from Hansenula saturnus.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
N50 K51 K54 N79 C200 T202 G203 T205 Y295 E296 L323 G324 G325
Binding residue
(residue number reindexed from 1)
N50 K51 K54 N79 C200 T202 G203 T205 Y295 E296 L323 G324 G325
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K51 Y269 Y295
Catalytic site (residue number reindexed from 1)
K51 Y269 Y295
Enzyme Commision number
3.5.99.7
: 1-aminocyclopropane-1-carboxylate deaminase.
Gene Ontology
Molecular Function
GO:0008660
1-aminocyclopropane-1-carboxylate deaminase activity
GO:0016787
hydrolase activity
GO:0019148
D-cysteine desulfhydrase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0009310
amine catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1f2d
,
PDBe:1f2d
,
PDBj:1f2d
PDBsum
1f2d
PubMed
10938279
UniProt
Q7M523
|1A1D_CYBSA 1-aminocyclopropane-1-carboxylate deaminase
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