Align 2-deoxy-D-ribonate transporter 2 (characterized)
to candidate BWI76_RS23725 BWI76_RS23725 MFS transporter
Query= reanno::Koxy:BWI76_RS23725 (445 letters) >FitnessBrowser__Koxy:BWI76_RS23725 Length = 445 Score = 901 bits (2328), Expect = 0.0 Identities = 445/445 (100%), Positives = 445/445 (100%) Query: 1 MTTINQTPAGEQGAKKRLIHRFSWVSLLVCWLIWVLNAYDREMILRLGPVISKEFSLSPE 60 MTTINQTPAGEQGAKKRLIHRFSWVSLLVCWLIWVLNAYDREMILRLGPVISKEFSLSPE Sbjct: 1 MTTINQTPAGEQGAKKRLIHRFSWVSLLVCWLIWVLNAYDREMILRLGPVISKEFSLSPE 60 Query: 61 QWGNVVALIMVALAVLDIPGSIWSDRYGSGWKRARFQVPLVLGYTALSFISGIKAISHGL 120 QWGNVVALIMVALAVLDIPGSIWSDRYGSGWKRARFQVPLVLGYTALSFISGIKAISHGL Sbjct: 61 QWGNVVALIMVALAVLDIPGSIWSDRYGSGWKRARFQVPLVLGYTALSFISGIKAISHGL 120 Query: 121 TAFVLLRVGVNLGAGWGEPVGVSNTAEWWPKEKRGFALGVHHTGYPIGALLSGVVASLVL 180 TAFVLLRVGVNLGAGWGEPVGVSNTAEWWPKEKRGFALGVHHTGYPIGALLSGVVASLVL Sbjct: 121 TAFVLLRVGVNLGAGWGEPVGVSNTAEWWPKEKRGFALGVHHTGYPIGALLSGVVASLVL 180 Query: 181 SAFGEGSWRYCFLLALIVAIPLMIFWAKYSTADRINTLYQHIDSQGMTRPATQESSHVAK 240 SAFGEGSWRYCFLLALIVAIPLMIFWAKYSTADRINTLYQHIDSQGMTRPATQESSHVAK Sbjct: 181 SAFGEGSWRYCFLLALIVAIPLMIFWAKYSTADRINTLYQHIDSQGMTRPATQESSHVAK 240 Query: 241 GEGMKTFLRTLRNRNISLTAGNTLLTQIVYMGINVVLPPYLYHVSGLSLAASAGLSIIFT 300 GEGMKTFLRTLRNRNISLTAGNTLLTQIVYMGINVVLPPYLYHVSGLSLAASAGLSIIFT Sbjct: 241 GEGMKTFLRTLRNRNISLTAGNTLLTQIVYMGINVVLPPYLYHVSGLSLAASAGLSIIFT 300 Query: 301 LTGTLGQIIWPWLSDSFGRKRTLIVCGLWMSIGIALFYFATNMPRLIAIQLFFGLVANAV 360 LTGTLGQIIWPWLSDSFGRKRTLIVCGLWMSIGIALFYFATNMPRLIAIQLFFGLVANAV Sbjct: 301 LTGTLGQIIWPWLSDSFGRKRTLIVCGLWMSIGIALFYFATNMPRLIAIQLFFGLVANAV 360 Query: 361 WPIYYAMASDSAEERATSTANGIITTAMFIGGGLSPLLMGWLIQFGGGWENPAGYIYAFF 420 WPIYYAMASDSAEERATSTANGIITTAMFIGGGLSPLLMGWLIQFGGGWENPAGYIYAFF Sbjct: 361 WPIYYAMASDSAEERATSTANGIITTAMFIGGGLSPLLMGWLIQFGGGWENPAGYIYAFF 420 Query: 421 TMAGCALLGMLLQLMTTDKTPRKAH 445 TMAGCALLGMLLQLMTTDKTPRKAH Sbjct: 421 TMAGCALLGMLLQLMTTDKTPRKAH 445 Lambda K H 0.325 0.139 0.443 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: 877 Number of extensions: 25 Number of successful extensions: 1 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: 445 Length of database: 445 Length adjustment: 32 Effective length of query: 413 Effective length of database: 413 Effective search space: 170569 Effective search space used: 170569 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: 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