Structure of PDB 4by3 Chain A Binding Site BS02
Receptor Information
>4by3 Chain A (length=362) Species:
9606
(Homo sapiens) [
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KLVRLPGLIDVHVHLREPGGTHKEDFASGTAAALAGGITMVCAMPNTRPP
IIDAPALALAQKLAEAGARCDFALFLGASSENAGTLGTVAGSAAGLKLYL
NETFSELRLDSVVQWMEHFETWPSHLPIVAHAEQQTVAAVLMVAQLTQRS
VHICHVARKEEILLIKAAKARGLPVTCEVAPHHLFLSHDDLERLGPGKGE
VRPELGSRQDVEALWENMAVIDCFASDHAPHTLEEKCGSRPPPGFPGLET
MLPLLLTAVSEGRLSLDDLLQRLHHNPRRIFHLPPQEDTYVEVDLEHEWT
IPSHMPFSKAHWTPFEGQKVKGTVRRVVLRGEVAYIDGQVLVPPGYGQDV
RKWPQGAVPQLP
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
4by3 Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
4by3
Structure, Functional Characterization, and Evolution of the Dihydroorotase Domain of Human Cad.
Resolution
1.73 Å
Binding residue
(original residue number in PDB)
K1556 H1590 H1614
Binding residue
(residue number reindexed from 1)
K97 H131 H155
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.1.3.2
: aspartate carbamoyltransferase.
3.5.1.2
: glutaminase.
3.5.2.3
: dihydroorotase.
6.3.4.16
: carbamoyl-phosphate synthase (ammonia).
6.3.5.5
: carbamoyl-phosphate synthase (glutamine-hydrolyzing).
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0016810
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
GO:0016812
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides
View graph for
Molecular Function
External links
PDB
RCSB:4by3
,
PDBe:4by3
,
PDBj:4by3
PDBsum
4by3
PubMed
24332717
UniProt
P27708
|PYR1_HUMAN Multifunctional protein CAD (Gene Name=CAD)
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