Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate Pf1N1B4_4287 Inositol transport system permease protein
Query= uniprot:D8IZC8 (344 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4287 Length = 340 Score = 208 bits (529), Expect = 2e-58 Identities = 133/323 (41%), Positives = 198/323 (61%), Gaps = 28/323 (8%) Query: 36 PVLVVLYLLFYGLTLYLSGDG-----TSNFASAENTMNILRQVAINLVLAAGMTFVILTA 90 P + ++L+ G+ L G S +++ + ++ QV+I +LA G+T VI+T Sbjct: 21 PTELSIFLVLIGIGLVFEMFGWIVRDQSFLMNSQRLVLMILQVSIIGLLAIGVTQVIITT 80 Query: 91 GIDLSVGSVLAVSAVLGMQV------------SLGAAPGWAIPMFIFSG--LVMGMVNGA 136 GIDLS GSVLA+SA++ + SL P W IP+ + G L+ G +NG+ Sbjct: 81 GIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLPVW-IPVIVGLGVGLLAGAINGS 139 Query: 137 MVALLNINAFVVTLGTMTAFRGAAYLLADGTTV-LNNDIPSFEWIGNGDFLHVPWLIWVA 195 ++A+ I F+ TLG M + RG A +G V + +D S+ IG+G +P +I++ Sbjct: 140 IIAITGIPPFIATLGMMVSARGLARYYTEGQPVSMLSD--SYTAIGHGA---MPVIIFLV 194 Query: 196 VAVVLLSWVILRKTVLGMHIYAIGGNLQAARLTGIRVGLVLLFVYSISGLFSGLAGAMSA 255 VAV+ + LR T G + YAIGGN+QAAR +GI V L+ VYSI+GL +GLAG +++ Sbjct: 195 VAVIF--HIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLVIVYSIAGLLAGLAGVVAS 252 Query: 256 SRLYGANGNWGSGYELDAIAAVVLGGTSLMGGVGSIWGTVVGALIIGVMNNGLTILGLSS 315 +R G YELDAIAA V+GGTSL GGVG I GTV+GALI+GVM +G T +G+ + Sbjct: 253 ARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASGFTFVGVDA 312 Query: 316 FWQYVAKGAVIVLAVILDKWRQK 338 + Q + KG +IV+AV++D++R K Sbjct: 313 YIQDIIKGLIIVVAVVIDQYRNK 335 Lambda K H 0.324 0.138 0.417 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: 325 Number of extensions: 15 Number of successful extensions: 4 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: 344 Length of database: 340 Length adjustment: 29 Effective length of query: 315 Effective length of database: 311 Effective search space: 97965 Effective search space used: 97965 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 49 (23.5 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