GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Acidovorax sp. GW101-3H11

Align L-iditol 2-dehydrogenase (EC 1.1.1.14) (characterized)
to candidate Ac3H11_2939 D-arabinitol 4-dehydrogenase (EC 1.1.1.11)

Query= BRENDA::Q9KWR5
         (485 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2939
          Length = 463

 Score =  238 bits (606), Expect = 4e-67
 Identities = 141/392 (35%), Positives = 209/392 (53%), Gaps = 8/392 (2%)

Query: 28  IVHFGVGNFFRAHEAFYVEQILEH-APDWAIVGVGLTGSDRSKKKAEEFKAQDCLYSLTE 86
           I+H G+G+F RAH+A Y+ Q+ +  + DWAI G  L         A   +AQ   Y+L  
Sbjct: 4   ILHLGLGSFHRAHQAVYMHQLRQQGSTDWAIAGGNLRPDMADTIAA--LQAQGGRYTLET 61

Query: 87  TAPSGKSTVRVMGALRDYLLAPADPEAVLKHLVDPAIRIVSMTITEGGYNINETTGAFDL 146
             P G+ +  V+ +++  +    D   ++    DPA RI+S T+TE GY ++        
Sbjct: 62  VTPQGERSYTVIESIQRVIPYQDDLAPLIAAGADPATRIISFTVTEAGYYLDAANQLDWA 121

Query: 147 ENAAVKADLKNPEKPS---TVFGYVVEALRRRWDAGGKAFTVMSCDNLRHNGNVARKAFL 203
             A ++ADL   +      T++G +   LR R  AG    T+M+CDNLRHNG+ +R   L
Sbjct: 122 TFADLRADLATVQAGQAGHTIYGGLASILRARMRAGAGPVTLMNCDNLRHNGDRSRGGLL 181

Query: 204 GYAKAR-DPELAKWIEENATFPNGMVDRITPTVSAEIAKKLNAASGLDDDLPLVAEDFHQ 262
            +  A  D  L  W+E+N T PN MVDRITP  + ++A+++  A+G DD   L+ E F Q
Sbjct: 182 QFIDALGDAPLKGWVEQNTTSPNAMVDRITPRPTPDVAERVKTATGWDDKAALMGESFIQ 241

Query: 263 WVLEDQFADGRPPLEKAGVQMVGDVTDWEYVKIRMLNAGHVMLCFPGILVGYENVDDAIE 322
           WV+ED F  GRP  EK GV+MV  V   E  KIR+LNA H  + + G L GY+ + +   
Sbjct: 242 WVIEDDFIAGRPAWEKVGVEMVQSVQAHEEAKIRLLNATHSCIAWAGTLAGYQYIHEGTH 301

Query: 323 DSELLGNLKNYLNKDVIPTLKAPSGMTLEGYRDSVISRFSNKAMSDQTLRIASDGCSKVQ 382
           D+ +     +Y+  D IP L  P  + LE YRD V+ RF N A++D   R+A D  SK+ 
Sbjct: 302 DAAIRQMAHDYVTDDAIPVL-LPCPIDLEAYRDVVLDRFGNPAIADTNQRVAMDAFSKIP 360

Query: 383 VFWTETVRRAIEDKRDLSRIAFGIASYLEMLR 414
                T+R  +   +    +A   A +L  L+
Sbjct: 361 GMIAPTIRDKLARNQPFDSVAVLPALFLAYLQ 392


Lambda     K      H
   0.317    0.135    0.398 

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: 543
Number of extensions: 21
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: 485
Length of database: 463
Length adjustment: 33
Effective length of query: 452
Effective length of database: 430
Effective search space:   194360
Effective search space used:   194360
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: 51 (24.3 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