Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate GFF2249 HP15_2199 glucose/sorbosone dehydrogenase
Query= BRENDA::I7A144 (352 letters) >FitnessBrowser__Marino:GFF2249 Length = 511 Score = 197 bits (501), Expect = 5e-55 Identities = 128/344 (37%), Positives = 176/344 (51%), Gaps = 39/344 (11%) Query: 23 VEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFRE----GRLSTYAELPVYHRGESGLL 78 VE + GLE PW+LAFLP GG L+ ER GR+R+ E G+ PV++ ++GL Sbjct: 173 VETLTSGLEHPWSLAFLPGGGALVTERAGRLRMISEEWELGQAPITGVPPVFNDAQAGLF 232 Query: 79 GLALHPRFPEAPYVYAYRTVAEGGLRNQVVRLRHLGERGVLDRV-VLDGIPARPHGLHSG 137 + L P F V+ + + V L + + V + PA+ H G Sbjct: 233 DVLLSPDFENNQLVFLAYSCGTASANHLCVARGQLQAEALTEVVEIFRAKPAKEGSAHYG 292 Query: 138 GRIAFGPDGMLYVTTGEVYE-RELAQDLASLGGKILRLTPEGEPAPGNPFLGRRGARPEV 196 GR+A+ PDG L VT G+ ++ RE AQ+L+S GKI+RL P+G NPF+GR GA PE+ Sbjct: 293 GRMAWLPDGTLIVTLGDGFDYREQAQNLSSHLGKIVRLNPDGSVPADNPFVGREGALPEI 352 Query: 197 YSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRVVGRGND-- 254 YS GHRN QGL + L + EHGP G DE+N+I PG NYGWP V+ G D Sbjct: 353 YSYGHRNVQGLVFDSVENVLIAHEHGPR-----GGDEINIIEPGHNYGWP-VITHGIDYT 406 Query: 255 ----------PRYRDPLYFWPQGFPPGNLAFFRGDLY--------VAGLRGQALLRLVLE 296 PL W P + +RG+L+ V L +++ R+ LE Sbjct: 407 GAMITPFVEREGMEQPLLHWTPSIAPSGMTRYRGELFPDWQGNLLVGALADKSVHRVTLE 466 Query: 297 -GERGRWRVLRVETALSGFG-RLREVQVGPDGALYVTTSNRDGR 338 GE VE+ G R+R+V GPDGA+Y+ T + DGR Sbjct: 467 AGEAS-----DVESLFEAMGERIRDVATGPDGAVYLLTDSADGR 505 Lambda K H 0.322 0.146 0.460 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: 576 Number of extensions: 39 Number of successful extensions: 8 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: 352 Length of database: 511 Length adjustment: 32 Effective length of query: 320 Effective length of database: 479 Effective search space: 153280 Effective search space used: 153280 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: 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