Species | Akkermansia muciniphila_A | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Verrucomicrobiota; Verrucomicrobiae; Verrucomicrobiales; Akkermansiaceae; Akkermansia; Akkermansia muciniphila_A | |||||||||||
CAZyme ID | MGYG000001881_00514 | |||||||||||
CAZy Family | GH77 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 237831; End: 239690 Strand: - |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GH77 | 11 | 554 | 6.4e-134 | 0.951417004048583 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
pfam02446 | Glyco_hydro_77 | 3.92e-120 | 11 | 553 | 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 | 2.11e-99 | 1 | 552 | 1 | 475 | 4-alpha-glucanotransferase; Provisional |
COG1640 | MalQ | 3.17e-84 | 4 | 555 | 11 | 496 | 4-alpha-glucanotransferase [Carbohydrate transport and metabolism]. |
PRK14510 | PRK14510 | 1.18e-76 | 5 | 576 | 723 | 1220 | bifunctional glycogen debranching protein GlgX/4-alpha-glucanotransferase. |
TIGR00217 | malQ | 2.00e-54 | 1 | 496 | 10 | 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 |
---|---|---|---|---|---|
QQR33694.1 | 0.0 | 1 | 619 | 5 | 623 |
ANU60608.1 | 0.0 | 1 | 619 | 5 | 623 |
ASB36253.1 | 0.0 | 1 | 619 | 5 | 623 |
QWP00094.1 | 0.0 | 1 | 619 | 1 | 619 |
QWP43301.1 | 0.0 | 1 | 619 | 1 | 619 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
1X1N_A | 3.06e-41 | 2 | 552 | 23 | 499 | 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 | 6.18e-41 | 2 | 552 | 75 | 551 | PotatoD-enzyme, native (substrate free) [Solanum tuberosum] |
1TZ7_A | 4.61e-39 | 5 | 452 | 22 | 423 | Aquifexaeolicus amylomaltase [Aquifex aeolicus],1TZ7_B Aquifex aeolicus amylomaltase [Aquifex aeolicus] |
2OWC_A | 5.27e-38 | 1 | 457 | 4 | 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] |
1CWY_A | 1.29e-37 | 1 | 457 | 1 | 421 | CrystalStructure Of Amylomaltase From Thermus Aquaticus, A Glycosyltransferase Catalysing The Production Of Large Cyclic Glucans [Thermus aquaticus],1ESW_A X-Ray Structure Of Acarbose Bound To Amylomaltase From Thermus Aquaticus. Implications For The Synthesis Of Large Cyclic Glucans [Thermus aquaticus] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q9Z8L2 | 1.87e-59 | 8 | 551 | 26 | 502 | 4-alpha-glucanotransferase OS=Chlamydia pneumoniae OX=83558 GN=malQ PE=3 SV=1 |
O34022 | 5.38e-58 | 8 | 551 | 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 | 2.44e-54 | 8 | 551 | 30 | 506 | 4-alpha-glucanotransferase OS=Chlamydia trachomatis (strain D/UW-3/Cx) OX=272561 GN=malQ PE=3 SV=1 |
Q9PKU9 | 4.18e-51 | 8 | 551 | 30 | 506 | 4-alpha-glucanotransferase OS=Chlamydia muridarum (strain MoPn / Nigg) OX=243161 GN=malQ PE=3 SV=1 |
P72785 | 1.12e-42 | 1 | 438 | 1 | 405 | 4-alpha-glucanotransferase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) OX=1111708 GN=malQ PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
0.999995 | 0.000045 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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