| Species | Akkermansia muciniphila | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lineage | Bacteria; Verrucomicrobiota; Verrucomicrobiae; Verrucomicrobiales; Akkermansiaceae; Akkermansia; Akkermansia muciniphila | |||||||||||
| CAZyme ID | MGYG000002454_00821 | |||||||||||
| CAZy Family | GH77 | |||||||||||
| CAZyme Description | 4-alpha-glucanotransferase | |||||||||||
| CAZyme Property |
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| Genome Property |
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| Gene Location | Start: 985137; End: 987008 Strand: - | |||||||||||
| Family | Start | End | Evalue | family coverage |
|---|---|---|---|---|
| GH77 | 15 | 558 | 3.2e-133 | 0.951417004048583 |
| Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
|---|---|---|---|---|---|---|---|
| pfam02446 | Glyco_hydro_77 | 3.59e-121 | 15 | 557 | 1 | 459 | 4-alpha-glucanotransferase. These enzymes EC:2.4.1.25 transfer a segment of a (1,4)-alpha-D-glucan to a new 4-position in an acceptor, which may be glucose or (1,4)-alpha-D-glucan. |
| PRK14508 | PRK14508 | 2.63e-101 | 5 | 556 | 1 | 475 | 4-alpha-glucanotransferase; Provisional |
| COG1640 | MalQ | 4.56e-85 | 8 | 559 | 11 | 496 | 4-alpha-glucanotransferase [Carbohydrate transport and metabolism]. |
| PRK14510 | PRK14510 | 8.00e-75 | 9 | 580 | 723 | 1220 | bifunctional glycogen debranching protein GlgX/4-alpha-glucanotransferase. |
| TIGR00217 | malQ | 2.50e-56 | 2 | 500 | 7 | 474 | 4-alpha-glucanotransferase. This enzyme is known as amylomaltase and disproportionating enzyme. [Energy metabolism, Biosynthesis and degradation of polysaccharides] |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
|---|---|---|---|---|---|
| QAA69318.1 | 0.0 | 1 | 623 | 1 | 623 |
| QTF04675.1 | 0.0 | 1 | 623 | 1 | 623 |
| QAA62562.1 | 0.0 | 1 | 623 | 1 | 623 |
| QHV21729.1 | 0.0 | 1 | 623 | 1 | 623 |
| QAA67062.1 | 0.0 | 1 | 623 | 1 | 623 |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| 1X1N_A | 3.23e-44 | 2 | 485 | 19 | 460 | Structuredetermination and refinement at 1.8 A resolution of Disproportionating Enzyme from Potato [Solanum tuberosum],6LX1_A Potato D-enzyme complexed with Acarbose [Solanum tuberosum],6LX2_A Potato D-enzyme complexed with CA26 [Solanum tuberosum] |
| 7COV_A | 6.98e-44 | 2 | 485 | 71 | 512 | PotatoD-enzyme, native (substrate free) [Solanum tuberosum] |
| 1TZ7_A | 2.58e-39 | 9 | 555 | 22 | 483 | Aquifexaeolicus amylomaltase [Aquifex aeolicus],1TZ7_B Aquifex aeolicus amylomaltase [Aquifex aeolicus] |
| 2OWC_A | 1.59e-38 | 3 | 461 | 2 | 423 | Structureof a covalent intermediate in Thermus thermophilus amylomaltase [Thermus thermophilus],2OWW_A Covalent intermediate in amylomaltase in complex with the acceptor analog 4-deoxyglucose [Thermus thermophilus],2OWX_A THERMUS THERMOPHILUS AMYLOMALTASE AT pH 5.6 [Thermus thermophilus] |
| 1FP8_A | 5.33e-38 | 5 | 461 | 1 | 421 | StructureOf The Amylomaltase From Thermus Thermophilus Hb8 In Space Group P21212 [Thermus thermophilus],1FP9_A Structure Of Amylomaltase From Thermus Thermophilus Hb8 In Space Group C2 [Thermus thermophilus] |
| Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
|---|---|---|---|---|---|---|
| Q9Z8L2 | 5.43e-61 | 12 | 555 | 26 | 502 | 4-alpha-glucanotransferase OS=Chlamydia pneumoniae OX=83558 GN=malQ PE=3 SV=1 |
| O34022 | 1.59e-60 | 12 | 555 | 30 | 506 | 4-alpha-glucanotransferase OS=Chlamydia caviae (strain ATCC VR-813 / DSM 19441 / 03DC25 / GPIC) OX=227941 GN=malQ PE=3 SV=1 |
| O84089 | 2.69e-55 | 3 | 555 | 21 | 506 | 4-alpha-glucanotransferase OS=Chlamydia trachomatis (strain D/UW-3/Cx) OX=272561 GN=malQ PE=3 SV=1 |
| Q9PKU9 | 3.38e-52 | 3 | 555 | 21 | 506 | 4-alpha-glucanotransferase OS=Chlamydia muridarum (strain MoPn / Nigg) OX=243161 GN=malQ PE=3 SV=1 |
| Q06801 | 3.82e-43 | 2 | 485 | 71 | 512 | 4-alpha-glucanotransferase, chloroplastic/amyloplastic OS=Solanum tuberosum OX=4113 GN=DPEP PE=1 SV=1 |
| Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
|---|---|---|---|---|---|
| 1.000068 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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