GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Phaeobacter inhibens BS107

Align 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (EC 1.2.4.4) (characterized)
to candidate GFF1731 PGA1_c17550 pyruvate dehydrogenase E1 component subunit alpha

Query= BRENDA::Q72GU1
         (367 letters)



>FitnessBrowser__Phaeo:GFF1731
          Length = 337

 Score =  149 bits (377), Expect = 8e-41
 Identities = 103/322 (31%), Positives = 159/322 (49%), Gaps = 4/322 (1%)

Query: 32  DLEGEKLRRLYRDMLAARMLDERYTILIRTGKTS-FIAPAAGHEAAQVAIAHAIRPGFDW 90
           ++  ++L   YR+ML  R  +E+   L   G    F     G EA  V +  A   G D 
Sbjct: 11  NVSADELLEYYREMLLIRRFEEKAGQLYGMGLIGGFCHLYIGQEAVVVGLEAAAEDG-DK 69

Query: 91  VFPYYRDHGLALALGIPLKELFGQMLATKADPNKGRQMPEHPGSKALNFFTVASPIASHV 150
               YRDHG  LA G+    +  ++   +   +KG+    H  SK  +F+     + + V
Sbjct: 70  RVTSYRDHGHMLACGMDPSGVMAELTGREGGYSKGKGGSMHMFSKEKHFYGGHGIVGAQV 129

Query: 151 PPAAGAAISMKLLRTGQVAVCTFGDGATSEGDWYAGINFAAVQGAPAVFVCENNFYAISV 210
           P  AG A S K     +V    FGDGA ++G  Y   N A +   P VFV ENN YA+  
Sbjct: 130 PLGAGLAFSDKYKGNDRVTFAYFGDGAANQGQVYETYNMAQLWDLPVVFVIENNQYAMGT 189

Query: 211 DYRHQTHSPTIADKAHAFGIPGYLVDGMDVLASYYVVKEAVERARRGEGPSLVELRVYRY 270
             +  T SP +  +  A+GI G  VDGMDVLA     + AV   R G+GP ++E++ YRY
Sbjct: 190 SVQRSTKSPALWKRGEAYGIKGEEVDGMDVLAVKEAGERAVAHCRAGKGPYILEVKTYRY 249

Query: 271 GPHSSADDDSRYRPKEEVAFWR-KKDPIPRFRRFLEARGLWNEEWEEDVREEIRAELERG 329
             HS + D ++YR +EEV   R ++DPI + R  L       E+  + + +EI+  + + 
Sbjct: 250 RGHSMS-DPAKYRTREEVQKMREERDPIEQVRDMLLTGKHATEDDLKAIDKEIKDIVNKS 308

Query: 330 LKEAEEAGPVPPEWMFADVFAE 351
              ++E+     E ++ D++A+
Sbjct: 309 ADFSKESPEPALEELWTDIYAD 330


Lambda     K      H
   0.320    0.138    0.426 

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: 346
Number of extensions: 25
Number of successful extensions: 1
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: 367
Length of database: 337
Length adjustment: 29
Effective length of query: 338
Effective length of database: 308
Effective search space:   104104
Effective search space used:   104104
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 (21.8 bits)
S2: 49 (23.5 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