Align alcohol dehydrogenase (EC 1.1.1.1); all-trans-retinol dehydrogenase (NAD+) (EC 1.1.1.105) (characterized)
to candidate AZOBR_RS16515 AZOBR_RS16515 S-(hydroxymethyl)glutathione dehydrogenase
Query= BRENDA::C7R702 (374 letters) >lcl|FitnessBrowser__azobra:AZOBR_RS16515 AZOBR_RS16515 S-(hydroxymethyl)glutathione dehydrogenase Length = 372 Score = 635 bits (1638), Expect = 0.0 Identities = 307/370 (82%), Positives = 338/370 (91%) Query: 5 VIKCKAAVAWEAGKPLSIEEVEVQPPQKGEVRVKIVATGVCHTDAFTLSGDDPEGVFPSI 64 ++K +AAVAWEA +PL IEEVEV P++GEV V+IVATGVCHTDA+TLSG D EGVFP+I Sbjct: 1 MVKSRAAVAWEAKRPLEIEEVEVAAPRQGEVLVRIVATGVCHTDAYTLSGMDSEGVFPAI 60 Query: 65 LGHEGGGIVESVGEGVTSVKPGDHVIPLYTPECGDCKFCLSGKTNLCQKIRETQGKGLMP 124 LGHEG GIVE VG GVTSV+ GDHVIPLYTPECG CKFCLSGKTNLCQ IR TQGKGLMP Sbjct: 61 LGHEGAGIVEEVGPGVTSVQVGDHVIPLYTPECGKCKFCLSGKTNLCQAIRATQGKGLMP 120 Query: 125 DGTTRFSINGKPIYHYMGTSTFSEYTVLPEISLAKVNPKAPLEEVCLLGCGVTTGMGAVM 184 DGT+RF+ G+P++HYMGTSTFSEYTVLPEI++AK+N APLE+VCLLGCGVTTGMGAV Sbjct: 121 DGTSRFTAKGQPVFHYMGTSTFSEYTVLPEIAVAKINKAAPLEKVCLLGCGVTTGMGAVR 180 Query: 185 NTAKVEEGATVAIFGLGGIGLSAVIGAVMAKASRIIAIDINESKFELAKKLGATDCVNPK 244 NTAKVE G+TVAIFGLGGIGLSA+IGAVMAKASRII IDIN KFE+AK+LGATD VNPK Sbjct: 181 NTAKVEPGSTVAIFGLGGIGLSAIIGAVMAKASRIIGIDINPDKFEIAKQLGATDVVNPK 240 Query: 245 DYDKPIQEVIVEMTDGGVDYSFECIGNVNVMRSALECCHKGWGESVIIGVAGAGQEISTR 304 DYD+PIQEV+VEMTDGGVDYSFECIGNV VMR+ALECCHKGWGESVIIGVAGAG+EISTR Sbjct: 241 DYDRPIQEVLVEMTDGGVDYSFECIGNVKVMRAALECCHKGWGESVIIGVAGAGEEISTR 300 Query: 305 PFQLVTGRVWKGTAFGGVKGRSELPDYVERYLAGEFKLDDFITHTMPLEKINDAFDLMHE 364 PFQLVTGRVW+G+AFGGV+GRSELPDYVERYL GEF+LD FITHTM LE IN AFDLMHE Sbjct: 301 PFQLVTGRVWRGSAFGGVRGRSELPDYVERYLKGEFELDTFITHTMGLEDINKAFDLMHE 360 Query: 365 GKSIRSVIHY 374 GKSIRSVI Y Sbjct: 361 GKSIRSVILY 370 Lambda K H 0.317 0.137 0.413 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: 628 Number of extensions: 19 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: 374 Length of database: 372 Length adjustment: 30 Effective length of query: 344 Effective length of database: 342 Effective search space: 117648 Effective search space used: 117648 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: 50 (23.9 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