Align SmoE, component of Hexitol (glucitol; mannitol) porter (characterized)
to candidate SMc01496 SMc01496 sorbitol-binding periplasmic protein
Query= TCDB::O30831 (436 letters) >FitnessBrowser__Smeli:SMc01496 Length = 436 Score = 711 bits (1834), Expect = 0.0 Identities = 336/430 (78%), Positives = 382/430 (88%), Gaps = 1/430 (0%) Query: 8 LMGACAVAALSSAAGAETITVATVNNGDMIRMQGLMSEFNAQHPDITVEWVTLEENVLRQ 67 L+G C+ AL+ A AET+T+ATVNNGDMIRMQ L +F +++PDI +EWVTLEENVLRQ Sbjct: 7 LLGTCSAVALAGLAQAETLTIATVNNGDMIRMQKLTDDFTSKNPDIQLEWVTLEENVLRQ 66 Query: 68 KVTTDIATKGGQFDVLTIGTYEVPIWGKQGWLVSLNDLPPEYDADDILPAIRNGLTVDGE 127 +VTTDIATKGGQ+D++TIGTYEVPIW KQGWL+ L+DL PEYD DD+LPAIR+GLT+DG+ Sbjct: 67 RVTTDIATKGGQYDIMTIGTYEVPIWAKQGWLLPLDDLGPEYDVDDLLPAIRSGLTIDGK 126 Query: 128 LYAAPFYGESSMIMYRKDLMEKAGLTMPDAPTWDFVKEAAQKMTDKDAEVYGICLRGKAG 187 LYAAPFYGESSM+MYRKDL EKAGLTMPDAPTWDF+ +AA+K+TDK E+YGICLRGKAG Sbjct: 127 LYAAPFYGESSMVMYRKDLFEKAGLTMPDAPTWDFIADAARKITDKGNEIYGICLRGKAG 186 Query: 188 WGENMAFLSAMANSYGARWFDENWQPQFDGEAWKATLTDYLDMMTNYGPPGASKNGFNEN 247 WGENMAFL+A AN++GARWFDENW+PQFD WK L Y+ +M + GPPGAS NGFNEN Sbjct: 187 WGENMAFLTATANAFGARWFDENWKPQFDQPEWKNALDFYVKLMNDAGPPGASSNGFNEN 246 Query: 248 LALFQQGKCGMWIDATVAASFVTNPEESTVADKVGFALAPDTGKGKRANWLGAWNLAIPA 307 L+LFQ GKCGMWIDATVAASFVTNP+ESTVADKVGFALAPDTG GKR NWL AWNLAIPA Sbjct: 247 LSLFQTGKCGMWIDATVAASFVTNPKESTVADKVGFALAPDTGLGKRGNWLWAWNLAIPA 306 Query: 308 GSQKVDAAKQFIAWATSKDYAELVASKEGWANVPPGTRTSLYENPEYQK-VPFAKMTLDS 366 GSQK ++A++FIAWAT KDY +LVA KEGWANVPPGTRTSLYENPEYQK PFAKMTLDS Sbjct: 307 GSQKAESAQKFIAWATGKDYLKLVAEKEGWANVPPGTRTSLYENPEYQKAAPFAKMTLDS 366 Query: 367 INAADPTHPAVDPVPYVGVQFVAIPEFQGIGTAVGQQFSAALAGSMSAEQALQAAQQFTT 426 INAADP +PAV PVPYVGVQFVAIPEFQG+GTAVGQ FSAALAG MS +QAL +AQQ +T Sbjct: 367 INAADPKNPAVKPVPYVGVQFVAIPEFQGLGTAVGQVFSAALAGQMSVDQALASAQQLST 426 Query: 427 REMTRAGYIK 436 REMT+AGYIK Sbjct: 427 REMTKAGYIK 436 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: 778 Number of extensions: 18 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: 436 Length adjustment: 32 Effective length of query: 404 Effective length of database: 404 Effective search space: 163216 Effective search space used: 163216 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