Species | Prevotellamassilia sp900540885 | |||||||||||
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Lineage | Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Bacteroidaceae; Prevotellamassilia; Prevotellamassilia sp900540885 | |||||||||||
CAZyme ID | MGYG000002930_00074 | |||||||||||
CAZy Family | GT0 | |||||||||||
CAZyme Description | D-inositol-3-phosphate glycosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 74512; End: 76323 Strand: + |
MRIAYISNNN PRDINNWSGT PYHIISALSK YHEVDWVGGG TLHGALWHHR FLNNKKPFNL | 60 |
LDYNEDIGHV VSNFVKDGKY DIAISSTYSM CSFLDIDIPL IAFSDLTYNL CTTYLKRAPD | 120 |
ELKEQAMQIE KDFLQLADAI IYPSSFAKDA AMADYNIEEN KIHILDFGAN IPTPVGVKVD | 180 |
EFESDICKLV FIGRNWVKKG GNKALATYSL LKTQGFPCEL TIIGCEPPYK VEDSDVKVFP | 240 |
WLDKSNADDL LLYDKIMRES HFLILPTEFD AYGIVFCEAS AYGIPSLAPN VGGVSQPIRE | 300 |
GLNGYLLSSH ASASDYAEKI KTIFQDKEKY RTLRLTSRNE YDTRLNWDIW TKSMNTIMDN | 360 |
VVRDKQIKRV ENNYGIIEKV ENEKGAEADS FYIPVYAFNL KSRPDRLAHL QHQFEDKPEF | 420 |
KVTHITAIKH DIGAIGLWES ICKAVAMAQK QNEDIIVLCE DDHEFTQYYS VDYLLSNIAE | 480 |
AYAQGAELLN GGIGGFGNAV PVDTNRSCVD WFWCTQFVVL FAPIFSKILN YDFKEGDTAD | 540 |
GVLSHIADSP QVMYPPISTQ KDFGYSDIIQ RQPMFQNRLF YSCNKRLASI HSVYQKYLRG | 600 |
SKY | 603 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
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cd03801 | GT4_PimA-like | 9.23e-33 | 2 | 354 | 1 | 361 | phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea. |
COG0438 | RfaB | 3.35e-19 | 1 | 365 | 1 | 381 | Glycosyltransferase involved in cell wall bisynthesis [Cell wall/membrane/envelope biogenesis]. |
cd03808 | GT4_CapM-like | 2.73e-14 | 129 | 349 | 132 | 356 | capsular polysaccharide biosynthesis glycosyltransferase CapM and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. CapM in Staphylococcus aureus is required for the synthesis of type 1 capsular polysaccharides. |
cd01635 | Glycosyltransferase_GTB-type | 1.53e-11 | 162 | 307 | 85 | 235 | glycosyltransferase family 1 and related proteins with GTB topology. Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. |
cd03811 | GT4_GT28_WabH-like | 1.78e-11 | 74 | 340 | 78 | 342 | family 4 and family 28 glycosyltransferases similar to Klebsiella WabH. This family is most closely related to the GT1 family of glycosyltransferases. WabH in Klebsiella pneumoniae has been shown to transfer a GlcNAc residue from UDP-GlcNAc onto the acceptor GalUA residue in the cellular outer core. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
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QUB69923.1 | 2.13e-202 | 1 | 593 | 1 | 580 |
QUB60703.1 | 6.06e-202 | 1 | 593 | 1 | 580 |
QUB82181.1 | 6.95e-201 | 1 | 593 | 1 | 580 |
BCA48826.1 | 4.09e-174 | 1 | 590 | 1 | 574 |
ALJ43352.1 | 2.33e-173 | 1 | 590 | 1 | 574 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q48453 | 6.65e-08 | 111 | 308 | 111 | 308 | Uncharacterized 41.2 kDa protein in cps region OS=Klebsiella pneumoniae OX=573 PE=4 SV=1 |
Q5YP47 | 1.10e-06 | 255 | 335 | 312 | 391 | D-inositol 3-phosphate glycosyltransferase OS=Nocardia farcinica (strain IFM 10152) OX=247156 GN=mshA PE=3 SV=1 |
A0JZ09 | 1.37e-06 | 189 | 326 | 228 | 371 | D-inositol 3-phosphate glycosyltransferase OS=Arthrobacter sp. (strain FB24) OX=290399 GN=mshA PE=3 SV=1 |
A1R8N8 | 3.08e-06 | 176 | 326 | 214 | 365 | D-inositol 3-phosphate glycosyltransferase OS=Paenarthrobacter aurescens (strain TC1) OX=290340 GN=mshA PE=3 SV=1 |
D1BD84 | 7.33e-06 | 118 | 348 | 150 | 404 | D-inositol 3-phosphate glycosyltransferase OS=Sanguibacter keddieii (strain ATCC 51767 / DSM 10542 / NCFB 3025 / ST-74) OX=446469 GN=mshA PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
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1.000058 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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