Structure of PDB 4wuo Chain B

Receptor sequence
>4wuoB (length=345) Species: 300852 (Thermus thermophilus HB8) [Search protein sequence]
MKVAVLPGDGIGPEVTEAALKVLRALDEAEGLGLAYEVFPFGGAAIDAFG
EPFPEPTRKGVEEAEAVLLGSVGGPKWDGLPRKIRPETGLLSLRKSQDLF
ANLRPAKVFPGLERLSPLKEEIARGVDVLIVRELTGGIYFGEPRGMSEAE
AWNTERYSKPEVERVARVAFEAARKRRKHVVSVDKANVLEVGEFWRKTVE
EVGRGYPDVALEHQYVDAMAMHLVRSPARFDVVVTGNIFGDILSDLASVL
PGSLGLLPSASLGRGTPVFAPVHGSAPDIAGKGIANPTAAILSAAMMLEH
AFGLVELARKVEDAVAKALLETPPPDLGGSAGTEAFTATVLRHLA
3D structure
PDB4wuo Glutamate 270 plays an essential role in K(+)-activation and domain closure of Thermus thermophilus isopropylmalate dehydrogenase.
ChainB
Resolution2.05 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) Y139 K185 D217 D241 D245
Catalytic site (residue number reindexed from 1) Y139 K185 D217 D241 D245
Enzyme Commision number 1.1.1.85: 3-isopropylmalate dehydrogenase.
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 IPM B R94 R104 R132 Y139 D241 R94 R104 R132 Y139 D241
BS02 NAD B I11 V72 G73 E87 L90 G255 H273 G274 S275 A276 D278 I279 N286 I11 V72 G73 E87 L90 G255 H273 G274 S275 A276 D278 I279 N286
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0003862 3-isopropylmalate dehydrogenase activity
GO:0016491 oxidoreductase activity
GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0042802 identical protein binding
GO:0046872 metal ion binding
GO:0051287 NAD binding
Biological Process
GO:0009098 L-leucine biosynthetic process
Cellular Component
GO:0005737 cytoplasm
GO:0005829 cytosol

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:4wuo, PDBe:4wuo, PDBj:4wuo
PDBsum4wuo
PubMed25497013
UniProtQ5SIY4|LEU3_THET8 3-isopropylmalate dehydrogenase (Gene Name=leuB)

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