Align SmoE, component of Hexitol (glucitol; mannitol) porter (characterized)
to candidate GFF1305 PGA1_c13210 extracellular solute-binding protein
Query= TCDB::O30831 (436 letters) >FitnessBrowser__Phaeo:GFF1305 Length = 433 Score = 649 bits (1675), Expect = 0.0 Identities = 315/429 (73%), Positives = 355/429 (82%), Gaps = 2/429 (0%) Query: 7 ALMGACAVAALSS-AAGAETITVATVNNGDMIRMQGLMSEFNAQHPDITVEWVTLEENVL 65 AL A A+ +S AA A+TIT+ATVNNGDMIRMQGL +F A+ VEWVTLEENVL Sbjct: 6 ALRAATALTVFASTAAFADTITIATVNNGDMIRMQGLTEDFTAKTGH-EVEWVTLEENVL 64 Query: 66 RQKVTTDIATKGGQFDVLTIGTYEVPIWGKQGWLVSLNDLPPEYDADDILPAIRNGLTVD 125 RQ+VTTDI+ KGGQFD++TIG YE PIWGK GWLV LNDLP +YD DDILPA+R GL+ D Sbjct: 65 RQRVTTDISAKGGQFDIMTIGMYETPIWGKNGWLVPLNDLPADYDVDDILPAMRGGLSHD 124 Query: 126 GELYAAPFYGESSMIMYRKDLMEKAGLTMPDAPTWDFVKEAAQKMTDKDAEVYGICLRGK 185 G L+AAPFYGESSMIMYR DLMEKAGL MP APTWDFV +AA++MTDKD E YGICLRGK Sbjct: 125 GTLFAAPFYGESSMIMYRTDLMEKAGLEMPAAPTWDFVADAARQMTDKDNETYGICLRGK 184 Query: 186 AGWGENMAFLSAMANSYGARWFDENWQPQFDGEAWKATLTDYLDMMTNYGPPGASKNGFN 245 AGWGEN AF++AM+NS+GARWFDENW PQFD EAW TL Y++++ + GPPGAS NGFN Sbjct: 185 AGWGENAAFITAMSNSFGARWFDENWAPQFDSEAWSNTLNFYINLLNDAGPPGASNNGFN 244 Query: 246 ENLALFQQGKCGMWIDATVAASFVTNPEESTVADKVGFALAPDTGKGKRANWLGAWNLAI 305 ENL+LFQQGKCGMWIDATVAASFVTNP +STVADKVGFALAPDTG GKR+NWL AW LAI Sbjct: 245 ENLSLFQQGKCGMWIDATVAASFVTNPNDSTVADKVGFALAPDTGLGKRSNWLWAWALAI 304 Query: 306 PAGSQKVDAAKQFIAWATSKDYAELVASKEGWANVPPGTRTSLYENPEYQKVPFAKMTLD 365 PAG+QK AAK+FI WATSKDY ELVA EGWANVPPG R SLYEN Y+ +PFAKMTL+ Sbjct: 305 PAGTQKEAAAKEFIQWATSKDYIELVAENEGWANVPPGARISLYENANYKDIPFAKMTLE 364 Query: 366 SINAADPTHPAVDPVPYVGVQFVAIPEFQGIGTAVGQQFSAALAGSMSAEQALQAAQQFT 425 SI +ADP +P VDPVPYVG+QF AIPEF GI T VGQ+FSAALAG +AE+AL AQ T Sbjct: 365 SILSADPNNPTVDPVPYVGIQFAAIPEFAGIATQVGQEFSAALAGQQTAEEALAKAQALT 424 Query: 426 TREMTRAGY 434 EM AGY Sbjct: 425 ADEMEAAGY 433 Lambda K H 0.316 0.131 0.400 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 745 Number of extensions: 24 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 436 Length of database: 433 Length adjustment: 32 Effective length of query: 404 Effective length of database: 401 Effective search space: 162004 Effective search space used: 162004 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory