GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Algoriphagus machipongonensis PR1

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_153231861.1 ALPR1_RS04230 PQQ-dependent sugar dehydrogenase

Query= BRENDA::Q8ZUN8
         (371 letters)



>NCBI__GCF_000166275.1:WP_153231861.1
          Length = 343

 Score =  158 bits (399), Expect = 2e-43
 Identities = 109/337 (32%), Positives = 174/337 (51%), Gaps = 24/337 (7%)

Query: 38  ISEVASDLEVPWSIAPLGGGRYLVTERPGRLVLISP---SGKKLVASFDVANVGEAGLLG 94
           +  + + LE PW +  L  G  LVTE+ G +++      +G+K+    +V  +G+ GLL 
Sbjct: 5   VDTLHTGLENPWGMTWLADGTLLVTEKKGEILIFREDEFTGEKIQGLPEVRTIGQGGLLD 64

Query: 95  LALHPEFPKKSWVYLYASYFAEGGHIRNRVIRGRLDGSTFKLKEVKTLIDGIPGAYIHNG 154
           +  HP + +  W+Y+  +           ++R RLDG+    +E   +         H G
Sbjct: 65  IQAHPNYGENGWLYISYAKKVTEEEGTTTIMRFRLDGNNAVDQEELIMSQPAWKGGNHFG 124

Query: 155 GRIRFGPDGMLYITTGDAAD-PRLAQDLSSLAGKILRVDEEGRPPADNPFPNSP-----I 208
            RI F  DG LY ++GD  D P  AQDL++  GKI R+ ++GR P DNPF ++P     I
Sbjct: 125 SRIVFDNDGYLYYSSGDRFDTPGNAQDLTNSHGKIHRIHDDGRIPTDNPFVDTPGAVASI 184

Query: 209 WSYGHRNPQGIDWHRASGVMVATEHGPVGHDEVNIILKGGNYGWP-LATGKAGRG----E 263
           W+YG+RNPQG+ + +A+  +  +EHGP G DE+N+I KG NYGWP ++ G    G    E
Sbjct: 185 WAYGNRNPQGLYFDKANNRLWESEHGPKGGDELNLIEKGNNYGWPEISYGINYDGTVLTE 244

Query: 264 FVDPV-IDTGSETWAPS----GASFVHGDMFPGLRGWLLIACLRGSMLAAVNFGDNMEVR 318
           F +   ++  +  + PS    G + V  D +P  +G +LI  L  + +  V+  +  E  
Sbjct: 245 FTEKEGMEQPATYYVPSIATAGITMVTSDRYPAWKGDILIGALAKTHINRVDM-EGTEAL 303

Query: 319 KISTFFKNVFGRLRDVVIDDDGGILISTSNRDGRGSL 355
                 +++ GR+R V    DG +   T   +G G L
Sbjct: 304 SQEIMLQDI-GRVRQVKESPDGYLYAIT---EGTGLL 336


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: 398
Number of extensions: 27
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: 343
Length adjustment: 29
Effective length of query: 342
Effective length of database: 314
Effective search space:   107388
Effective search space used:   107388
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