GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Dechlorosoma suillum PS

Align glyoxylate reductase (EC 1.1.1.26); 4-hydroxybutyrate dehydrogenase (EC 1.1.1.61); glyoxylate reductase (NADP+) (EC 1.1.1.79) (characterized)
to candidate Dsui_3438 Dsui_3438 beta-hydroxyacid dehydrogenase, 3-hydroxyisobutyrate dehydrogenase

Query= BRENDA::Q9LSV0
         (289 letters)



>FitnessBrowser__PS:Dsui_3438
          Length = 299

 Score =  136 bits (342), Expect = 6e-37
 Identities = 90/290 (31%), Positives = 143/290 (49%), Gaps = 6/290 (2%)

Query: 1   MEVGFLGLGIMGKAMSMNLLKNGFKVTVWNRTLSKCDELVEHGASVCESPAEVIKKCKYT 60
           ME+GF+GLGIMG+ M++NLLK G  V VW R       L+E GA  C SPA V  + +  
Sbjct: 1   MEIGFIGLGIMGRPMALNLLKGGHGVHVWARRPESMAPLLEAGAVGCSSPAAVAGQVEVV 60

Query: 61  IAMLSDPCAALSVVFDKGGVLEQICEGKGY-----IDMSTVDAETSLKINEAITGKGGRF 115
           I+M++D      V+    GV     EG G      +DMST+    +  +   +  +G  F
Sbjct: 61  ISMVADAPDVAQVMLGPDGVAAG-AEGAGKHGLVAVDMSTIAPAAARDLAARLQARGVDF 119

Query: 116 VEGPVSGSKKPAEDGQLIILAAGDKALFEESIPAFDVLGKRSFYLGQVGNGAKMKLIVNM 175
           V+ PVSG +  A  G L I+A G    F +++PAF  LG+   ++G  G G   K    +
Sbjct: 120 VDAPVSGGEVGAIAGSLSIMAGGSAEAFAKALPAFLCLGQNVVHVGAAGAGQVAKACNQI 179

Query: 176 IMGSMMNAFSEGLVLADKSGLSSDTLLDILDLGAMTNPMFKGKGPSMNKSSYPPAFPLKH 235
           + G  + A +E    A ++G+    + + L  G   + + +  G  M + ++ P F    
Sbjct: 180 VTGMGVLAVAEAFNFARQAGVDPAKVREALLGGFAYSRILENHGQRMLERNFKPGFKSWM 239

Query: 236 QQKDMRLALALGDENAVSMPVAAAANEAFKKARSLGLGDLDFSAVIEAVK 285
            QKD+ + +    E  + +P AAA  + F      GL + D  AV++ ++
Sbjct: 240 HQKDLNIVMQSAHELGLCLPGAAATAQMFNAMVGSGLEEEDSVAVLKLLE 289


Lambda     K      H
   0.317    0.134    0.379 

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: 203
Number of extensions: 5
Number of successful extensions: 2
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: 289
Length of database: 299
Length adjustment: 26
Effective length of query: 263
Effective length of database: 273
Effective search space:    71799
Effective search space used:    71799
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 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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