Structure of PDB 2rab Chain A

Receptor sequence
>2rabA (length=451) Species: 1048 (Marichromatium gracile) [Search protein sequence]
TQHFDLIAIGGGSGGLAVAEKAAAFGKRVALIESKALGGTCVNVGCVPKK
VMWYASHLAEAVRDAPGFGVQASTLDWPRLVAGRDRYIGAINSFWDGYVE
RLGITRVDGHARFVDAHTIEVEGQRLSADHIVIATGGRPIVPRLPGAELG
ITSDGFFALQQQPKRVAIIGAGYIGIELAGLLRSFGSEVTVVALEDRLLF
QFDPLLSATLAENMHAQGIETHLEFAVAALERDAQGTTLVAQDGTRLGFD
SVIWAVGRAPNTRDLGLEAAGIEVQSNGMVPTDAYQNTNVPGVYALGDIT
GRDQLTPVAIAAGRRLAERLFDGQSERKLDYDNIPTVVFAHPPLSKVGLS
EPEARERLGDVLTVYETSFTPMRYALNEHGPKTAMKLVCAGPEQRVVGVH
VIGDGADEMLQGFAVAVKMGATKADFDNTVAIHPGSAEELVTLKEPVRRP
G
3D structure
PDB2rab Understanding nicotinamide dinucleotide cofactor and substrate specificity in class I flavoprotein disulfide oxidoreductases: crystallographic analysis of a glutathione amide reductase.
ChainA
Resolution2.5 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) S14 L38 C42 C47 K50 Y176 E180 I314 A435 H437 E442
Catalytic site (residue number reindexed from 1) S13 L37 C41 C46 K49 Y173 E177 I310 A431 H433 E438
Enzyme Commision number 1.8.1.16: glutathione amide reductase.
Interaction with ligand
Gene Ontology
Molecular Function
GO:0000166 nucleotide binding
GO:0004362 glutathione-disulfide reductase (NADPH) activity
GO:0016491 oxidoreductase activity
GO:0016668 oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
GO:0046872 metal ion binding
GO:0050660 flavin adenine dinucleotide binding
GO:0050661 NADP binding
Biological Process
GO:0006749 glutathione metabolic process
GO:0034599 cellular response to oxidative stress
GO:0045454 cell redox homeostasis
GO:0098869 cellular oxidant detoxification
Cellular Component
GO:0005829 cytosol

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Molecular Function

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Cellular Component
External links
PDB RCSB:2rab, PDBe:2rab, PDBj:2rab
PDBsum2rab
PubMed17977556
UniProtD0VWY5|GASHR_MARGR Glutathione amide reductase (Gene Name=garB)

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