Structure of PDB 2a5h Chain D Binding Site BS06
Receptor Information
>2a5h Chain D (length=410) Species:
1550
(Clostridium subterminale) [
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NRRYELFKDVSDADWNDWRWQVRNRIETVEELKKYIPLTKEEEEGVAQCV
KSLRMAITPYYLSLIDPNDPNDPVRKQAIPTALELNKAAADLEDPLHEDT
DSPVPGLTHRYPDRVLLLITDMCSMYCRHCTRRRFAGQSDDSMPMERIDK
AIDYIRNTPQVRDVLLSGGDALLVSDETLEYIIAKLREIPHVEIVRIGSR
TPVVLPQRITPELVNMLKKYHPVWLNTHFNHPNEITEESTRACQLLADAG
VPLGNQSVLLRGVNDCVHVMKELVNKLVKIRVRPYYIYQCDLSLGLEHFR
TPVSKGIEIIEGLRGHTSGYCVPTFVVDAPGGGGKTPVMPNYVISQSHDK
VILRNFEGVITTYSEPINYTPGCNCDVCTGKKKVHKVGVAGLLNGEGMAL
EPVGLERNKR
Ligand information
Ligand ID
SF4
InChI
InChI=1S/4Fe.4S
InChIKey
LJBDFODJNLIPKO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
[S]12[Fe]3[S]4[Fe]1[S]5[Fe]2[S]3[Fe]45
CACTVS 3.385
S1[Fe]S[Fe]1.S2[Fe]S[Fe]2
Formula
Fe4 S4
Name
IRON/SULFUR CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
2a5h Chain D Residue 418 [
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Receptor-Ligand Complex Structure
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PDB
2a5h
The X-ray crystal structure of lysine-2,3-aminomutase from Clostridium subterminale.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
C125 C129 C132 G171 R202 H230
Binding residue
(residue number reindexed from 1)
C123 C127 C130 G169 R200 H228
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R112 Y113 R116 C125 C129 C132 R134 D293 D330 K337
Catalytic site (residue number reindexed from 1)
R110 Y111 R114 C123 C127 C130 R132 D291 D328 K335
Enzyme Commision number
5.4.3.2
: lysine 2,3-aminomutase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016853
isomerase activity
GO:0046872
metal ion binding
GO:0050066
L-lysine 2,3-aminomutase activity
GO:0051536
iron-sulfur cluster binding
GO:0051539
4 iron, 4 sulfur cluster binding
Biological Process
GO:0019475
L-lysine catabolic process to acetate
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2a5h
,
PDBe:2a5h
,
PDBj:2a5h
PDBsum
2a5h
PubMed
16166264
UniProt
Q9XBQ8
|KAMA_CLOSU L-lysine 2,3-aminomutase (Gene Name=kamA)
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