Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_007694352.1 C447_RS12355 PQQ-dependent sugar dehydrogenase
Query= BRENDA::I7A144 (352 letters) >NCBI__GCF_000336675.1:WP_007694352.1 Length = 507 Score = 206 bits (525), Expect = 8e-58 Identities = 135/342 (39%), Positives = 181/342 (52%), Gaps = 33/342 (9%) Query: 23 VEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLSTYAELPVYHR----GESGLL 78 V+ V LE+PW AF D + ERPGRI G A+ R GE GLL Sbjct: 183 VDTVATNLEIPWGAAFRGDT-LYFTERPGRIMKVESGSGELVADFTDPTRANGYGEGGLL 241 Query: 79 GLALHPRFPEAPYVYAYRTVAEGG-LRNQVVRLRHLGERGVLDRVVLDGIPARPHGLHSG 137 GLA HP P+ YAY+T +G N+++ L G V+ DGI H G Sbjct: 242 GLAFHPDDPDT--AYAYQTYVDGDEAANRILELD--AASGFSSSVLFDGIEGADG--HDG 295 Query: 138 GRIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLTPEGEPAPGNPFLGRRGARPEVY 197 GR+A D LY T G+ E + AQD +SL G ++RLT +GEP P NPF G G P VY Sbjct: 296 GRLAIDGDA-LYATVGDTKEPQSAQDPSSLSGVVIRLTLDGEPHPDNPFDGDEG-HPAVY 353 Query: 198 SLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRVVGRGNDPRY 257 + GHRNPQGLA+ + GE++S+EHGP + DE+N++ G NYGWPR G ++ + Sbjct: 354 TYGHRNPQGLAF--RDGEVYSTEHGPDHD-----DEINVLEAGSNYGWPRASGTESEGEF 406 Query: 258 RDPLYFWPQGFPPGNLAFF-------RGDLYVAGLRGQALLRLVLEGERGRWRVLRVETA 310 + + PG+ F+ +GDL+ L G+ L R+ L+G + E Sbjct: 407 VGAIAAYTPTIAPGSATFYDGPISQWQGDLFFGTLSGEHLHRVRLDGH----DAVEEERL 462 Query: 311 LSG-FGRLREVQVGPDGALYVTTSNRDGRGQVRPGDDRVLRL 351 G +GR+R GPD LY+ TSNRDGRG DDR+LR+ Sbjct: 463 YEGEYGRIRTAFTGPDDHLYLATSNRDGRGSPVASDDRILRI 504 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: 653 Number of extensions: 50 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 352 Length of database: 507 Length adjustment: 32 Effective length of query: 320 Effective length of database: 475 Effective search space: 152000 Effective search space used: 152000 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: 50 (23.9 bits)
This GapMind analysis is from Sep 24 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:
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