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Literature summary for 3.1.1.117 extracted from
- Microbial glucuronoyl esterases 10 years after discovery (2016), Appl. Environ. Microbiol., 82, 7014-7018 .
Application
| Application | Comment | Organism |
|---|---|---|
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Thermothelomyces thermophilus |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Trichoderma reesei |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Podospora anserina |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Ruminococcus flavefaciens |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Schizophyllum commune |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Sodiomyces alcalophilus |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Phanerochaete carnosa |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Phanerodontia chrysosporium |
| biotechnology | glucuronoyl esterases are interesting candidates for biotechnological applications in plant biomass processing and genetic modification of plants | Teredinibacter turnerae |
Cloned(Commentary)
| Cloned (Comment) | Organism |
|---|---|
| gene cip2, the enzyme is homologously overexpressed using a cellobiohydrolase promoter and secreted to the growth medium | Trichoderma reesei |
Protein Variants
| Protein Variants | Comment | Organism |
|---|---|---|
| S217A | site-directed mutagenesis, mutation of thee catalytic serine, inactive mutant | Thermothelomyces thermophilus |
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Thermothelomyces thermophilus | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? |  |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Trichoderma reesei | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Podospora anserina | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Ruminococcus flavefaciens | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Schizophyllum commune | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Sodiomyces alcalophilus | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Phanerochaete carnosa | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Phanerodontia chrysosporium | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Teredinibacter turnerae | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Thermothelomyces thermophilus ATCC 42464 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Podospora anserina ATCC MYA-4624 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Podospora anserina DSM 980 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Phanerodontia chrysosporium ATCC MYA-4764 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Phanerodontia chrysosporium FGSC 9002 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Thermothelomyces thermophilus BCRC 31852 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Podospora anserina S | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Schizophyllum commune H4-8 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Teredinibacter turnerae ATCC 39867 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Trichoderma reesei QM6a | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Thermothelomyces thermophilus DSM 1799 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Schizophyllum commune FGSC 9210 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Teredinibacter turnerae T7901 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Phanerochaete carnosa HHB-10118-sp | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | Phanerodontia chrysosporium RP-78 | - |
4-O-methyl-D-glucuroxylan + methanol | - |
? | |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Phanerochaete carnosa | K5XDZ6 | Peniophora carnosa | - |
| Phanerochaete carnosa HHB-10118-sp | K5XDZ6 | Peniophora carnosa | - |
| Phanerodontia chrysosporium | P0CT87 | - |
- |
| Phanerodontia chrysosporium | P0CT87 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium | P0CT88 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium ATCC MYA-4764 | P0CT87 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium ATCC MYA-4764 | P0CT88 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium FGSC 9002 | P0CT87 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium FGSC 9002 | P0CT88 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium RP-78 | P0CT87 | - |
- |
| Phanerodontia chrysosporium RP-78 | P0CT87 | Sporotrichum pruinosum | - |
| Phanerodontia chrysosporium RP-78 | P0CT88 | Sporotrichum pruinosum | - |
| Podospora anserina | B2ABS0 | - |
- |
| Podospora anserina ATCC MYA-4624 | B2ABS0 | - |
- |
| Podospora anserina DSM 980 | B2ABS0 | - |
- |
| Podospora anserina S | B2ABS0 | - |
- |
| Ruminococcus flavefaciens | Q9RLB8 | - |
- |
| Ruminococcus flavefaciens | Q9RLB8 | a multidomain esterase composed of acetylxylan esterase, EC 3.1.1.72, and 4-O-methyl-glucuronoyl methylesterase | - |
| Schizophyllum commune | D8QLP9 | - |
- |
| Schizophyllum commune FGSC 9210 | D8QLP9 | - |
- |
| Schizophyllum commune H4-8 | D8QLP9 | - |
- |
| Sodiomyces alcalophilus | A0A1D8EJG8 | Acremonium alcalophilum | - |
| Teredinibacter turnerae | C5BN23 | - |
- |
| Teredinibacter turnerae ATCC 39867 | C5BN23 | - |
- |
| Teredinibacter turnerae T7901 | C5BN23 | - |
- |
| Thermothelomyces thermophilus | G2QJR6 | Sporotrichum thermophile | - |
| Thermothelomyces thermophilus ATCC 42464 | G2QJR6 | Sporotrichum thermophile | - |
| Thermothelomyces thermophilus BCRC 31852 | G2QJR6 | Sporotrichum thermophile | - |
| Thermothelomyces thermophilus DSM 1799 | G2QJR6 | Sporotrichum thermophile | - |
| Trichoderma reesei | G0RV93 | Trichoderma reesei | - |
| Trichoderma reesei | G0RV93 | i.e. Trichoderma reesei | - |
| Trichoderma reesei QM6a | G0RV93 | i.e. Trichoderma reesei | - |
Purification (Commentary)
| Purification (Comment) | Organism |
|---|---|
| recombinant Cip2 from cell growth medium | Trichoderma reesei |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Thermothelomyces thermophilus | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Trichoderma reesei | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Podospora anserina | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Ruminococcus flavefaciens | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Schizophyllum commune | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Sodiomyces alcalophilus | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Phanerochaete carnosa | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Phanerodontia chrysosporium | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Teredinibacter turnerae | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Thermothelomyces thermophilus ATCC 42464 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Podospora anserina ATCC MYA-4624 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Podospora anserina DSM 980 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Phanerodontia chrysosporium ATCC MYA-4764 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Phanerodontia chrysosporium FGSC 9002 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Thermothelomyces thermophilus BCRC 31852 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Podospora anserina S | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Schizophyllum commune H4-8 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Teredinibacter turnerae ATCC 39867 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Trichoderma reesei QM6a | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Thermothelomyces thermophilus DSM 1799 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Schizophyllum commune FGSC 9210 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Teredinibacter turnerae T7901 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Phanerochaete carnosa HHB-10118-sp | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| 4-O-methyl-D-glucuroxylan methyl ester + H2O | - |
Phanerodontia chrysosporium RP-78 | 4-O-methyl-D-glucuroxylan + methanol | - |
? | |
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Thermothelomyces thermophilus | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Trichoderma reesei | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Podospora anserina | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Ruminococcus flavefaciens | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Schizophyllum commune | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerochaete carnosa | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerodontia chrysosporium | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Teredinibacter turnerae | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides. The recombinant GE from Acremonium alcalophilum reduces the molecular mass of isolated lignin-carbohydrate complexes from spruce and birch | Sodiomyces alcalophilus | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcoholesters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerochaete carnosa | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Thermothelomyces thermophilus ATCC 42464 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Podospora anserina ATCC MYA-4624 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Podospora anserina DSM 980 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerodontia chrysosporium ATCC MYA-4764 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerodontia chrysosporium FGSC 9002 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Thermothelomyces thermophilus BCRC 31852 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Podospora anserina S | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Schizophyllum commune H4-8 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Teredinibacter turnerae ATCC 39867 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Trichoderma reesei QM6a | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Thermothelomyces thermophilus DSM 1799 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Schizophyllum commune FGSC 9210 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Teredinibacter turnerae T7901 | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerochaete carnosa HHB-10118-sp | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcoholesters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerochaete carnosa HHB-10118-sp | ? | - |
- |
|
| additional information | the enzyme GE enzymes are active on alkyl and alkyl aryl alcohol esters of MeGlcA and GlcA or their glycosides. The GEs do not differentiate esters of alpha- or beta-glucuronides | Phanerodontia chrysosporium RP-78 | ? | - |
- |
|
Subunits
| Subunits | Comment | Organism |
|---|---|---|
| More | multidomain structures of glucuronoyl esterases (GEs) | Thermothelomyces thermophilus |
| More | multidomain structures of glucuronoyl esterases (GEs) | Trichoderma reesei |
| More | multidomain structures of glucuronoyl esterases (GEs) | Podospora anserina |
| More | multidomain structures of glucuronoyl esterases (GEs) | Ruminococcus flavefaciens |
| More | multidomain structures of glucuronoyl esterases (GEs) | Schizophyllum commune |
| More | multidomain structures of glucuronoyl esterases (GEs) | Sodiomyces alcalophilus |
| More | multidomain structures of glucuronoyl esterases (GEs) | Phanerochaete carnosa |
| More | multidomain structures of glucuronoyl esterases (GEs) | Teredinibacter turnerae |
| More | multidomain structures of glucuronoyl esterases (GEs), Phanerochaete chrysosporium produces two enzyme forms, one without (GE2) and one with (GE1) the CBM1 module. The catalytic domains of the GEs are almost identical | Phanerodontia chrysosporium |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| 4-O-methyl-glucuronoyl methylesterase | UniProt | Ruminococcus flavefaciens |
| 4-O-methyl-glucuronoyl methylesterase | UniProt | Phanerochaete carnosa |
| 4-O-methyl-glucuronoyl methylesterase 1 | - |
Phanerodontia chrysosporium |
| 4-O-methyl-glucuronoyl methylesterase 1 | UniProt | Sodiomyces alcalophilus |
| 4-O-methyl-glucuronoyl methylesterase 2 | - |
Phanerodontia chrysosporium |
| carbohydrate esterase family 15 protein | UniProt | Phanerochaete carnosa |
| CesA | - |
Ruminococcus flavefaciens |
| Cip2 | - |
Trichoderma reesei |
| GCE | UniProt | Phanerochaete carnosa |
| GE1 | - |
Podospora anserina |
| GE1 | - |
Sodiomyces alcalophilus |
| GE1 | - |
Phanerodontia chrysosporium |
| Ge2 | - |
Phanerodontia chrysosporium |
| glucuronoyl esterase | - |
Thermothelomyces thermophilus |
| glucuronoyl esterase | - |
Trichoderma reesei |
| glucuronoyl esterase | - |
Podospora anserina |
| glucuronoyl esterase | - |
Ruminococcus flavefaciens |
| glucuronoyl esterase | - |
Schizophyllum commune |
| glucuronoyl esterase | - |
Sodiomyces alcalophilus |
| glucuronoyl esterase | - |
Phanerochaete carnosa |
| glucuronoyl esterase | - |
Phanerodontia chrysosporium |
| glucuronoyl esterase | - |
Teredinibacter turnerae |
| glucuronoyl esterase 1 | - |
Sodiomyces alcalophilus |
| glucuronoyl esterase 1 | - |
Phanerodontia chrysosporium |
| glucuronoyl esterase 2 | - |
Phanerodontia chrysosporium |
| More | cf. EC 3.1.1.72 | Ruminococcus flavefaciens |
| PHACADRAFT_157044 | locus name | Phanerochaete carnosa |
| PHACADRAFT_247750 | locus name | Phanerochaete carnosa |
| TERTU_0517 | - |
Teredinibacter turnerae |
Expression
| Organism | Comment | Expression |
|---|---|---|
| Phanerodontia chrysosporium | expression of genes encoding GE1 and GE2 isozymes appears to be mediated by different forms of regulatory control | additional information |
General Information
| General Information | Comment | Organism |
|---|---|---|
| evolution | the glucuronoyl esterases evolve for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Trichoderma reesei |
| evolution | the glucuronoyl esterases evolve for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Podospora anserina |
| evolution | the glucuronoyl esterases evolve for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Ruminococcus flavefaciens |
| evolution | the glucuronoyl esterases evolve for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Schizophyllum commune |
| evolution | the glucuronoyl esterases evolve for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Phanerodontia chrysosporium |
| evolution | the glucuronoyl esterases evolve for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Teredinibacter turnerae |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Thermothelomyces thermophilus |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Trichoderma reesei |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Podospora anserina |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Schizophyllum commune |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Sodiomyces alcalophilus |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. In Teredinibacter turnerae, a shipworm gut bacterium, GE is connected with endo-beta-1,4-xylanase of glycoside hydrolase (GH) family 11. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Teredinibacter turnerae |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. In the bacterium Ruminococcus flavefaciens, GE occurs in a bifunctional enzyme in combination with a catalytic module of an acetylxylan esterase. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Ruminococcus flavefaciens |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. The genome of the white-rot fungus and also the genome of its close relative Phanerochaete carnosa each contain three GE genes, two of which code for CBM-containing enzymes. The majority of the genomes of white-rot fungi contain two GE genes, whereas the genomes of brown-rot fungi contain usually only one CE15 gene. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Phanerodontia chrysosporium |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. The genome of the white-rot fungus and also the genome of its close relative Phanerochaete chrysosporium each contain three GE genes, two of which code for CBM-containing enzymes. The majority of the genomes of white-rot fungi contain two GE genes, whereas the genomes of brown-rot fungi contain usually only one CE15 gene. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Phanerochaete carnosa |
| evolution | the enzyme belongs to the family of carbohydrate esterases (CE15). The glucuronoyl esterases (GEs) evolved for hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. The genome of the white-rot fungus and also the genome of its close relative Phanerochaete chrysosporium each contain three GE genes, two of which code for CBM-scontaining enzymes. The majority of the genomes of white-rot fungi contain two GE genes, whereas the genomes of brown-rot fungi contain usually only one CE15 gene. Basidiomycetes have on average more genes in CE15 than do aspergilli, uneven GE gene distribution in microbial wood decay. Phylogenetic tree of confirmed and putative GEs, acetylxylan esterases, feruloyl esterases, and pectin methyl esterases, overview | Phanerochaete carnosa |
| metabolism | Phanerochaete chrysosporium produces two enzyme forms, one without (GE2) and one with (GE1) the CBM1 module. Expression of genes encoding GE1 and GE2 isozymes appears to be mediated by different forms of regulatory control | Phanerodontia chrysosporium |
| additional information | three-dimensional structure determination and analysis, the structure has an alpha/beta-hydrolase fold with an overall alphabetaalpha-sandwich architecture. The twisted beeta-sheet is sandwiched between two layers of alpha-helices with the catalytic triad Ser-His-Glu exposed on the protein surface | Thermothelomyces thermophilus |
| additional information | three-dimensional structure determination and analysis, the structure has an alpha/beta-hydrolase fold with an overall alphabetaalpha-sandwich architecture. The twisted beeta-sheet is sandwiched between two layers of alpha-helices with the catalytic triad Ser-His-Glu exposed on the protein surface | Trichoderma reesei |
| physiological function | the enzyme plays an important role in microbial breakdown of plant cell walls. The microbial enzyme hydrolyses the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Trichoderma reesei |
| physiological function | the enzyme plays an important role in microbial breakdown of plant cell walls. The microbial enzyme hydrolyses the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Podospora anserina |
| physiological function | the enzyme plays an important role in microbial breakdown of plant cell walls. The microbial enzyme hydrolyses the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Ruminococcus flavefaciens |
| physiological function | the enzyme plays an important role in microbial breakdown of plant cell walls. The microbial enzyme hydrolyses the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Schizophyllum commune |
| physiological function | the enzyme plays an important role in microbial breakdown of plant cell walls. The microbial enzyme hydrolyses the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Phanerodontia chrysosporium |
| physiological function | the enzyme plays an important role in microbial breakdown of plant cell walls. The microbial enzyme hydrolyses the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls | Teredinibacter turnerae |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Thermothelomyces thermophilus |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Trichoderma reesei |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Podospora anserina |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Ruminococcus flavefaciens |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Schizophyllum commune |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Sodiomyces alcalophilus |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Phanerochaete carnosa |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Phanerodontia chrysosporium |
| physiological function | glucuronoyl esterases (GEs) catalyze the hydrolysis of the ester linkages between 4-O-methyl-D-glucuronic acid of plant glucuronoxylans and lignin alcohols, one of the crosslinks in the plant cell walls. They have catalytic properties on artificial substrates and positive effect on enzymatic saccharification of plant biomass. The enzyme plays an important role in plant cell wall degradation | Teredinibacter turnerae |
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Release 2023.1 (January 2023)
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