GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fba in Azospirillum brasilense Sp245

Align Fructose-bisphosphate aldolase class 1; Fructose-bisphosphate aldolase class I; FBP aldolase; EC 4.1.2.13 (characterized)
to candidate AZOBR_RS10395 AZOBR_RS10395 fructose-bisphosphate aldolase

Query= SwissProt::P0A991
         (350 letters)



>FitnessBrowser__azobra:AZOBR_RS10395
          Length = 309

 Score =  169 bits (428), Expect = 9e-47
 Identities = 105/297 (35%), Positives = 154/297 (51%), Gaps = 11/297 (3%)

Query: 47  PAVLRNMQTLYNTGRLAGTGYLSILPVDQGVEHSAGASFAANPLYFDPKNIVELAIEAGC 106
           P V  N+  +   G+L GTG L ILPVDQG EH    SFA N   +DP    +LAI+AGC
Sbjct: 19  PGVKANLARILMEGKLGGTGKLVILPVDQGFEHGPARSFAPNEPGYDPHYHYQLAIDAGC 78

Query: 107 NCVASTYGVLASVSRRYAHRIPFLVKLNHNETLS-YPNTYDQTLYASVEQAFNMGAVAVG 165
           N  A+  G L + +  +A  IP ++K+N   +LS      DQ + ASV+ A  +G  A+G
Sbjct: 79  NAYAAPLGSLEAGASTFAGSIPLILKMNSANSLSRQKEDADQAVTASVQDALRLGCSAIG 138

Query: 166 ATIYFGSEESRRQIEEISAAFERAHELGMVTVLWAYLRNSAFKKDGVDYHVSADLTGQAN 225
            TIY GS+    Q EEI    + A  +G+ TVLW+Y R     K+G    ++ D+ G A 
Sbjct: 139 FTIYPGSDAMYDQYEEIRELSKEAKSVGLPTVLWSYPRGGTISKEG---ELAIDVIGYAA 195

Query: 226 HLAATIGADIVKQKMAENNGGYKAINYGYTDDRVYSKLTSENPIDLVRYQLANCYMGRAG 285
           H+AA +GA I+K K+   +         Y        +      D VR+ +   + GR  
Sbjct: 196 HMAALLGAHIIKVKLPSAHLEQAEAKKVYES----KNIPIATQADRVRHIMQCAFNGRRI 251

Query: 286 LINSGGAAGGETDLSDAVRTAVINKRAGGMGLILGRKAFKKSMADGVKLINAVQDVY 342
           ++ SGGA  GE  + +  R     +  GG G I+GR AF++   D +KL++ +  +Y
Sbjct: 252 VVFSGGATKGEDAVFEDARAI---RDGGGNGSIIGRNAFQRPREDALKLLDRIMKIY 305


Lambda     K      H
   0.318    0.134    0.386 

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: 261
Number of extensions: 10
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: 350
Length of database: 309
Length adjustment: 28
Effective length of query: 322
Effective length of database: 281
Effective search space:    90482
Effective search space used:    90482
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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