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 |
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Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |
| 1ff3B |
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Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |
| 1ff3C |
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Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |
| 1fvaA |
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Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |
| 1fvaB |
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Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |
| 1fvgA |
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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 |
|
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;TYR 82;GLU 94;TYR 134;CYS 198;CYS 206 | CAS 51 | |||
| 1ff3B |
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;TYR 82;GLU 94;TYR 134; ; | CAS 51 | invisible 195-211 | ||
| 1ff3C |
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;TYR 82;GLU 94;TYR 134; ; | CAS 51 | invisible 193-211 | ||
| 1fvaA |
|
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CYS 72;TYR 103;GLU 115;TYR 155;CYS 218;CYS 227 | ||||
| 1fvaB |
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CYS 72;TYR 103;GLU 115;TYR 155;CYS 218;CYS 227 | ||||
| 1fvgA |
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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 |
|---|
|
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 |