GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Lentibacillus jeotgali Grbi

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_040912248.1 ON01_RS02880 sorbosone dehydrogenase family protein

Query= BRENDA::Q8ZUN8
         (371 letters)



>NCBI__GCF_000224785.1:WP_040912248.1
          Length = 359

 Score =  226 bits (575), Expect = 1e-63
 Identities = 138/333 (41%), Positives = 193/333 (57%), Gaps = 25/333 (7%)

Query: 38  ISEVASDLEVPWSIAPLGGGRYLVTERPGRLVLISPSG---KKLVASFDVANVGEAGLLG 94
           I  +A +LEVPWSI  L    YL TER G +  I       + +    +V+   EAGLLG
Sbjct: 41  IEVIAENLEVPWSIEKLNNTFYL-TERSGSIAEIENGEVERQTVELEQEVSTGSEAGLLG 99

Query: 95  LALHPEFPKKSWVYLYASYFAEGGHIRNRVIRGRLDGSTFKLKEVKTLIDGIPGAYIHNG 154
             L P+F + +  Y Y +Y  +G    NR+I  RL+ + ++  E   L+D IP    H+G
Sbjct: 100 FVLAPDFSESNLAYAYYTY-EDGDDQFNRIITLRLEDNVWR--EESLLLDQIPSGAYHHG 156

Query: 155 GRIRFGPDGMLYITTGDAADPRLAQDLSSLAGKILRVDEEGRPPADNPFPNSPIWSYGHR 214
           GRI+ GPDG LY T GDA+D  +AQD  SL GKILR++ +G  P+DNPFP+S ++SYGHR
Sbjct: 157 GRIKIGPDGYLYATAGDASDSEIAQDPDSLGGKILRMNLDGSIPSDNPFPDSYVYSYGHR 216

Query: 215 NPQGIDWHRASGVMVATEHGPVGHDEVNIILKGGNYGWPLATGKAGRGEFVDPVIDTGSE 274
           NPQG+ W  + G + A+EHG   +DE+N I  G NYGWP+  G   +   V P   +G +
Sbjct: 217 NPQGLTW-TSDGTLYASEHGNDANDEINRIEAGQNYGWPVIEGNEEQEGMVTPRFTSGDD 275

Query: 275 -TWAPSGASFVHGDMFPGLRGWLLIACLRGSMLAAVNFG-DNMEVRKISTFFKNVFGRLR 332
            TWAPSG  +    ++        +A LRGS  A + F  +  E R++ T      GR+R
Sbjct: 276 STWAPSGMDYDDDKLY--------VAALRGS--AVIEFDLETGEHREVIT----GLGRIR 321

Query: 333 DVVIDDDGGILISTSNRDGRGSLRAGDDKILKI 365
           DV++DD     IS +NRDGRG+    DD++ +I
Sbjct: 322 DVLVDDSYLYFIS-NNRDGRGTPEESDDRLYRI 353


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: 410
Number of extensions: 28
Number of successful extensions: 5
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: 359
Length adjustment: 30
Effective length of query: 341
Effective length of database: 329
Effective search space:   112189
Effective search space used:   112189
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