GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Algiphilus aromaticivorans DG1253

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_043765331.1 U743_RS02685 PQQ-dependent sugar dehydrogenase

Query= BRENDA::Q8ZUN8
         (371 letters)



>NCBI__GCF_000733765.1:WP_043765331.1
          Length = 360

 Score =  133 bits (335), Expect = 7e-36
 Identities = 114/338 (33%), Positives = 157/338 (46%), Gaps = 30/338 (8%)

Query: 36  FKISEVASDLEVPWSIAPLGGGRYLVTERPGRLVLISPSGKKLVASFDVANV---GEAGL 92
           +++  VA  L+ PWS+A L  GR LVTER GRL +I   G        V  V    + GL
Sbjct: 22  YRVETVAEGLDHPWSLAFLPDGRMLVTERVGRLRVIGTDGSLSAPVEGVPAVHAESQGGL 81

Query: 93  LGLALHPEFPKKSWVYLYASYFAEG--GHIRNRVIRGRLDGSTFKLKEVKTLIDGIPGAY 150
             +    +F     +YL    +A+G  G     ++R RL+G      E            
Sbjct: 82  FDVLPARDFADSGQIYLS---YADGPAGANATALMRARLEGGELIASEPLFRAKPAKDTP 138

Query: 151 IHNGGRIRFGPDGMLYITTGDAADPR-LAQDLSSLAGKILRVDEEGRPPADNPFPNS--- 206
           +H GGR+ +  DG L +  GD  D R  AQD  +  G I+R+  +G  P DNPF +    
Sbjct: 139 VHYGGRMCWMADGTLLLGMGDGFDFREQAQDPDNHLGTIVRLTADGGVPEDNPFADGGGR 198

Query: 207 -PIWSYGHRNPQGIDWHRASGVMVATEHGPVGHDEVNIILKGGNYGWPLATGKA------ 259
             ++SYGHRN QG+    A GV+ A EHGP G DE+N I  G NYGWP+ TG        
Sbjct: 199 PEVYSYGHRNVQGLLCD-ADGVL-AHEHGPQGGDELNRIEAGANYGWPVVTGGLDYNNAR 256

Query: 260 -----GRGEFVDPVIDTGSETWAPSGASFVHGDMFPGLRGWLLIACLRGSMLAAVNF-GD 313
                 R   + P+++  + +  PSG     GD F   +G L +A L    +  V   GD
Sbjct: 257 VTPFDSRPGMLPPLLE-WTPSIGPSGLMRYTGDAFGEWQGDLFVATLVEPGVRRVRLRGD 315

Query: 314 NMEVRKISTFFKNVFGRLRDVVIDDDGGILISTSNRDG 351
             EV      F+    R+RDV    DG + + T   DG
Sbjct: 316 --EVLGQEVLFEAQGQRIRDVRNGPDGALYLLTDAADG 351


Lambda     K      H
   0.320    0.140    0.432 

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: 453
Number of extensions: 30
Number of successful extensions: 6
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: 371
Length of database: 360
Length adjustment: 30
Effective length of query: 341
Effective length of database: 330
Effective search space:   112530
Effective search space used:   112530
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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