Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate AZOBR_RS31355 AZOBR_RS31355 putative glucose dehydrogenase precursor
Query= BRENDA::I7A144 (352 letters) >FitnessBrowser__azobra:AZOBR_RS31355 Length = 386 Score = 186 bits (471), Expect = 1e-51 Identities = 131/357 (36%), Positives = 182/357 (50%), Gaps = 55/357 (15%) Query: 23 VEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFR-EGRLSTYAE-LP-VYHRGESGLLG 79 V+ V GL PW LAFLPDG ML+ E+ GR+R+ +G +S + +P V RG+ GLL Sbjct: 38 VKTVASGLSHPWGLAFLPDGRMLVTEKDGRLRIVAPDGTVSAPVKGVPKVDDRGQGGLLD 97 Query: 80 LALHPRFPEAPYVYAYRTV--AEGGLRNQVVRLRHLGERGVLD---------RVVLDGIP 128 +AL P F + +VY + E G + V RGVL+ RV+ P Sbjct: 98 VALDPEFAQNRFVYLSFSEPGTEDGTNSTAVA------RGVLNADETALTDVRVIFSQKP 151 Query: 129 ARPHGLHSGGRIAFGPDGMLYVTTGE---VYERELAQDLASLGGKILRLTPEGEPAPGNP 185 +H G R+ F G LYVT GE R AQDL S GK++R+ +G NP Sbjct: 152 KVESRMHYGSRLVFDRQGHLYVTLGERSLEQFRTQAQDLDSHLGKVVRINRDGSVPADNP 211 Query: 186 FLGRRGARPEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGW 245 F+ + GA PE++S GHRN QG A +P+TG L+ +EHGP G DEVN+ PG NYGW Sbjct: 212 FVNQSGALPEIWSYGHRNIQGAALNPQTGALWINEHGPR-----GGDEVNVPEPGKNYGW 266 Query: 246 PRV------------VGRGNDPRYRDPLYFWPQGFPPGNLAFF--------RGDLYVAGL 285 P V G+ + P +P+Y W + F+ +G L+ GL Sbjct: 267 PVVSYGVNYNGTPIGTGKSSAPGMEEPVYQWTPVIGSSGMTFYTADTLPGWKGSLFNGGL 326 Query: 286 RGQALLRLVLEGERGRWRVLRVETALSGFG-RLREVQVGPDGALYVTTSNRDGRGQV 341 + ++RL L+G +V E G R+R+V GPDGALY+ T + RG++ Sbjct: 327 ATKEVVRLELDGN----KVKHEERMFRDLGKRIRQVSQGPDGALYLLTD--ENRGEI 377 Score = 29.3 bits (64), Expect = 2e-04 Identities = 16/42 (38%), Positives = 23/42 (54%), Gaps = 12/42 (28%) Query: 139 RIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLTPEGEP 180 +++ GPDG LY+ T E G+ILR+TP G+P Sbjct: 357 QVSQGPDGALYLLTDENR------------GEILRVTPAGKP 386 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: 484 Number of extensions: 41 Number of successful extensions: 10 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 352 Length of database: 386 Length adjustment: 30 Effective length of query: 322 Effective length of database: 356 Effective search space: 114632 Effective search space used: 114632 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: 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