DB code: S00277
CATH domain | 3.30.1060.10 : Peptide Methionine Sulfoxide Reductase; Chain A | Catalytic domain |
---|---|---|
E.C. | 1.8.4.11 | |
CSA | 1ff3 1fva | |
M-CSA | 1ff3 1fva | |
MACiE | M0122 |
CATH domain | Related DB codes (homologues) |
---|---|
3.30.1060.10 : Peptide Methionine Sulfoxide Reductase; Chain A | S00523 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | RefSeq | Pfam |
---|---|---|---|---|
P0A744 |
Peptide methionine sulfoxide reductase msrA
|
Protein-methionine-S-oxide reductase
EC 1.8.4.11 Peptide-methionine (S)-S-oxide reductase Peptide Met(O) reductase |
NP_418640.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_492361.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF01625
(PMSR)
[Graphical View] |
P54149 |
Peptide methionine sulfoxide reductase
|
EC
1.8.4.11
Protein-methionine-S-oxide reductase Peptide-methionine (S)-S-oxide reductase Peptide Met(O) reductase |
NP_776539.1
(Protein)
NM_174114.2 (DNA/RNA sequence) |
PF01625
(PMSR)
[Graphical View] |
KEGG enzyme name |
---|
peptide-methionine (S)-S-oxide reductase
MsrA methionine sulfoxide reductase (ambiguous) methionine sulphoxide reductase A methionine S-oxide reductase (ambiguous) methionine S-oxide reductase (S-form oxidizing) methionine sulfoxide reductase A peptide methionine sulfoxide reductase |
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
P0A744 | MSRA_ECOLI | Peptide-L-methionine + thioredoxin disulfide + H(2)O = peptide-L-methionine (S)-S-oxide + thioredoxin. L-methionine + thioredoxin disulfide + H(2)O = L-methionine (S)-S-oxide + thioredoxin. | |||
P54149 | MSRA_BOVIN | Peptide-L-methionine + thioredoxin disulfide + H(2)O = peptide-L-methionine (S)-S-oxide + thioredoxin. L-methionine + thioredoxin disulfide + H(2)O = L-methionine (S)-S-oxide + thioredoxin. |
KEGG Pathways | Map code | Pathways | E.C. |
---|
Compound table | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Substrates | Products | Intermediates | |||||||||||
KEGG-id | C03895 | C00342 | C15999 | C03023 | C00343 | C00001 | C00073 | ||||||
E.C. | |||||||||||||
Compound | Peptide-L-methionine (S)-S-oxide | Reduced thioredoxin | L-methionine (S)-S-oxide | Peptide-L-methionine | Oxidized thioredoxin | H2O | L-methionine | ||||||
Type | peptide/protein,sulfoxide group | amide group,carbohydrate,peptide/protein,sulfhydryl group | amino acids,sulfoxide group | peptide/protein,sulfide group | amide group,carbohydrate,disulfide bond,peptide/protein | H2O | amino acids,sulfide group | ||||||
ChEBI |
49031 58772 49031 58772 |
15377 15377 |
16643 57844 16643 57844 |
||||||||||
PubChem |
10909908 11869257 10909908 11869257 |
22247451 962 22247451 962 |
6137 6992087 6137 6992087 |
||||||||||
1ff3A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1ff3B | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1ff3C | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1fvaA | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1fvaB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | ||||||
1fvgA | Unbound | Analogue:DTT | Unbound | Unbound | Unbound | Unbound | Intermediate-analogue:DTT |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
PDB;1fvg |
Active-site residues | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
PDB | Catalytic residues | Cofactor-binding residues | Modified residues | Main-chain involved in catalysis | Comment | |||||
1ff3A | ;TYR 82;GLU 94;TYR 134;CYS 198;CYS 206 | CAS 51 | ||||||||
1ff3B | ;TYR 82;GLU 94;TYR 134; ; | CAS 51 | invisible 195-211 | |||||||
1ff3C | ;TYR 82;GLU 94;TYR 134; ; | CAS 51 | invisible 193-211 | |||||||
1fvaA | CYS 72;TYR 103;GLU 115;TYR 155;CYS 218;CYS 227 | |||||||||
1fvaB | CYS 72;TYR 103;GLU 115;TYR 155;CYS 218;CYS 227 | |||||||||
1fvgA | CYS 72;TYR 103;GLU 115;TYR 155;CYS 218; | truncation 219-228 |
References for Catalytic Mechanism | ||
---|---|---|
References | Sections | No. of steps in catalysis |
[1]
|
Fig.3, p.13310-13311 | |
[2]
|
Fig.1, p.35911-35913 | |
[4]
|
Fig.3, p.6466-6467 | |
[5]
|
Fig.8, p.1175-1176 | |
[9]
|
Scheme 5, p.402-404 | |
[15]
|
p.4121-4125 |
References | |
---|---|
[1] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (1.6 ANGSTROMS) |
Medline ID | 20519025 |
PubMed ID | 11063566 |
Journal | Biochemistry |
Year | 2000 |
Volume | 39 |
Pages | 13307-12 |
Authors | Lowther WT, Brot N, Weissbach H, Matthews BW |
Title |
Structure and mechanism of peptide methionine sulfoxide reductase, |
Related PDB | 1fva 1fvg |
Related UniProtKB | P54149 |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10964927 |
Journal | J Biol Chem |
Year | 2000 |
Volume | 275 |
Pages | 35908-13 |
Authors | Boschi-Muller S, Azza S, Sanglier-Cianferani S, Talfournier F, Van Dorsselear A, Branlant G |
Title | A sulfenic acid enzyme intermediate is involved in the catalytic mechanism of peptide methionine sulfoxide reductase from Escherichia coli. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10799493 |
Journal | J Biol Chem |
Year | 2000 |
Volume | 275 |
Pages | 14167-72 |
Authors | Moskovitz J, Poston JM, Berlett BS, Nosworthy NJ, Szczepanowski R, Stadtman ER |
Title | Identification and characterization of a putative active site for peptide methionine sulfoxide reductase (MsrA) and its substrate stereospecificity. |
Related PDB | |
Related UniProtKB | |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 10841552 |
Journal | Proc Natl Acad Sci U S A |
Year | 2000 |
Volume | 97 |
Pages | 6463-8 |
Authors | Lowther WT, Brot N, Weissbach H, Honek JF, Matthews BW |
Title | Thiol-disulfide exchange is involved in the catalytic mechanism of peptide methionine sulfoxide reductase. |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11080639 |
Journal | Structure Fold Des |
Year | 2000 |
Volume | 8 |
Pages | 1167-78 |
Authors | Tete-Favier F, Cobessi D, Boschi-Muller S, Azza S, Branlant G, Aubry A |
Title | Crystal structure of the Escherichia coli peptide methionine sulphoxide reductase at 1.9 A resolution. |
Related PDB | 1ff3 |
Related UniProtKB | |
[6] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11311146 |
Journal | Biochem J |
Year | 2001 |
Volume | 355 |
Pages | 819-25 |
Authors | Petropoulos I, Mary J, Perichon M, Friguet B |
Title |
Rat peptide methionine sulphoxide reductase: cloning of the cDNA, |
Related PDB | |
Related UniProtKB | |
[7] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11430764 |
Journal | J Biomol NMR |
Year | 2001 |
Volume | 20 |
Pages | 97-8 |
Authors | Beraud S, Chambost JP, Bersch B, Gans P, Barras F, Marion D |
Title |
Backbone H(N), |
Related PDB | |
Related UniProtKB | |
[8] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11604533 |
Journal | Protein Sci |
Year | 2001 |
Volume | 10 |
Pages | 2272-9 |
Authors | Boschi-Muller S, Azza S, Branlant G |
Title |
E. |
Related PDB | |
Related UniProtKB | |
[9] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11860363 |
Journal | Curr Med Chem |
Year | 2002 |
Volume | 9 |
Pages | 385-409 |
Authors | Vaughan MD, Sampson PB, Honek JF |
Title | Methionine in and out of proteins: targets for drug design. |
Related PDB | |
Related UniProtKB | |
[10] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12431100 |
Journal | J Am Chem Soc |
Year | 2002 |
Volume | 124 |
Pages | 13709-15 |
Authors | Beraud S, Bersch B, Brutscher B, Gans P, Barras F, Blackledge M |
Title | Direct structure determination using residual dipolar couplings: reaction-site conformation of methionine sulfoxide reductase in solution. |
Related PDB | |
Related UniProtKB | |
[11] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11812798 |
Journal | J Biol Chem |
Year | 2002 |
Volume | 277 |
Pages | 12016-22 |
Authors | Olry A, Boschi-Muller S, Marraud M, Sanglier-Cianferani S, Van Dorsselear A, Branlant G |
Title |
Characterization of the methionine sulfoxide reductase activities of PILB, |
Related PDB | |
Related UniProtKB | |
[12] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11885278 |
Journal | Methods Enzymol |
Year | 2002 |
Volume | 348 |
Pages | 249-59 |
Authors | Davis DA, Newcomb FM, Moskovitz J, Fales HM, Levine RL, Yarchoan R |
Title | Reversible oxidation of HIV-2 protease. |
Related PDB | |
Related UniProtKB | |
[13] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11938352 |
Journal | Nat Struct Biol |
Year | 2002 |
Volume | 9 |
Pages | 348-52 |
Authors | Lowther WT, Weissbach H, Etienne F, Brot N, Matthews BW |
Title | The mirrored methionine sulfoxide reductases of Neisseria gonorrhoeae pilB. |
Related PDB | |
Related UniProtKB | |
[14] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11807942 |
Journal | Proteins |
Year | 2002 |
Volume | 46 |
Pages | 149-52 |
Authors | Gladyshev VN |
Title | Thioredoxin and peptide methionine sulfoxide reductase: convergence of similar structure and function in distinct structural folds. |
Related PDB | |
Related UniProtKB | |
[15] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12837786 |
Journal | J Bacteriol |
Year | 2003 |
Volume | 185 |
Pages | 4119-26 |
Authors | Taylor AB, Benglis DM Jr, Dhandayuthapani S, Hart PJ |
Title | Structure of Mycobacterium tuberculosis methionine sulfoxide reductase A in complex with protein-bound methionine. |
Related PDB | 1nwa |
Related UniProtKB |
Comments |
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The E.C. This enzyme catalyzes two successive raections (see [1], (A) Reduction of L-methionine S-oxide. (B) Reduction of active-site residues through oxidation of reduced thioredoxin. |
Created | Updated |
---|---|
2004-02-02 | 2009-02-26 |