Align L-iditol 2-dehydrogenase (EC 1.1.1.14) (characterized)
to candidate BWI76_RS07640 BWI76_RS07640 short chain dehydrogenase
Query= BRENDA::Q1J2J0 (255 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS07640 BWI76_RS07640 short chain dehydrogenase Length = 261 Score = 185 bits (470), Expect = 7e-52 Identities = 113/254 (44%), Positives = 145/254 (57%), Gaps = 13/254 (5%) Query: 13 LFRLDGRHALVTGGAQGIGFEIARGLAQAGARVTIADLNPDVG-----------EGAARE 61 LF L R A VTG GIG IA GLA AGARV DL D G G A Sbjct: 10 LFNLQDRVAFVTGAGSGIGQMIAYGLASAGARVVCFDLREDGGLAETVKNIEAIGGEACF 69 Query: 62 LDGTFERLNVTDADAVADLARRLPDVDVLVNNAGIVRNAPAEDTPDDDWRAVLSVNLDGV 121 G +L+ A VA R +D+ VN AGI PA + + W+ V+ +NL GV Sbjct: 70 YTGDVRQLSDLRA-GVALAKSRFGRLDIAVNAAGIANANPALEMETEQWQRVIDINLTGV 128 Query: 122 FWCCREFGRTMLARGRGAIVSTASMSGLISNHPQPQAAYNASKAAVIHLTRSLAGEWASR 181 + C+ M G G+I++ ASMSG+I N QA YN SKA VIHL++SLA EW + Sbjct: 129 WNSCKAEAELMQETGGGSIINIASMSGIIVNRGLDQAHYNCSKAGVIHLSKSLAMEWIGK 188 Query: 182 GVRVNAVAPGYTATPLTRRGLETPEWRETWLKETPLGRLAEPREIAPAVLYLASDAASFV 241 G+RVN+++PGYTATP+ R + RE + +TP+ R+A+ E+A L+LASDAASF Sbjct: 189 GIRVNSISPGYTATPMNTRPEMVHQTRE-FESQTPIQRMAKVEEMAGPALFLASDAASFC 247 Query: 242 TGHTLVVDGGYTVW 255 TG LVVDGG+ W Sbjct: 248 TGVDLVVDGGFVCW 261 Lambda K H 0.319 0.134 0.408 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: 200 Number of extensions: 7 Number of successful extensions: 3 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: 255 Length of database: 261 Length adjustment: 24 Effective length of query: 231 Effective length of database: 237 Effective search space: 54747 Effective search space used: 54747 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 47 (22.7 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