GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Marinobacter adhaerens HP15

Align isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate GFF1029 HP15_1008 acyl-CoA dehydrogenase domain protein

Query= BRENDA::P26440
         (426 letters)



>FitnessBrowser__Marino:GFF1029
          Length = 383

 Score =  249 bits (636), Expect = 1e-70
 Identities = 144/375 (38%), Positives = 214/375 (57%), Gaps = 5/375 (1%)

Query: 47  EEQRQLRQTMAKFLQEHLAPKAQEIDRSNEFKNLREFWKQLGNLGVLGITAPVQYGGSGL 106
           EE    R ++ K L++ + P  +  ++S      RE W  LGN G+L +  P ++GG G 
Sbjct: 8   EELAMFRDSVIKVLEKEVTPHYEAWEKSGLVP--RELWNTLGNAGMLCVDVPEEWGGIGA 65

Query: 107 GYLEHVLVMEEISRAS-GAVGLSYGAHSNLCINQLVRNGNEAQKEKYLPKLISGEYIGAL 165
            +   V+V EE++R   GA+  +   HS++    L   GNE Q++++LPKL+SGE +GA+
Sbjct: 66  PFQFSVVVGEELARMGFGALSTNVMVHSDIVAPYLSHMGNEEQRQQWLPKLVSGEAVGAI 125

Query: 166 AMSEPNAGSDVVSMKLKAEKKGNHYILNGNKFWITNGPDADVLIVYAKTDLAAVPASRGI 225
           AM+EP AGSD+ +++  A K G+ YILNG+K +ITNG  AD++IV AKTD  A   +RGI
Sbjct: 126 AMTEPGAGSDLQAIRTSAVKDGDEYILNGSKTFITNGQHADMVIVAAKTDPKA--GARGI 183

Query: 226 TAFIVEKGMPGFSTSKKLDKLGMRGSNTCELIFEDCKIPAANILGHENKGVYVLMSGLDL 285
           + F+V+  +PGFS  + LDK+G    +T EL F D +IPA+ +LG E +G   LM  L  
Sbjct: 184 SLFLVDTSLPGFSKGRNLDKIGQHSGDTSELFFSDMRIPASALLGEEGQGFVYLMKELPR 243

Query: 286 ERLVLAGGPLGLMQAVLDHTIPYLHVREAFGQKIGHFQLMQGKMADMYTRLMACRQYVYN 345
           ERLV+    +   +  LD TI Y   RE FGQK+   Q  + ++A M T     + +V  
Sbjct: 244 ERLVIGALGVAAARGSLDLTIAYAQERELFGQKLAQLQNTRFEIARMETDYRVNKAFVDQ 303

Query: 346 VAKACDEGHCTAKDCAGVILYSAECATQVALDGIQCFGGNGYINDFPMGRFLRDAKLYEI 405
                D G   A   +     + E   +VA   +Q FGG GY  ++P+ R   DA++  I
Sbjct: 304 CIDQYDLGELDAPTASMAKYSATEMQCRVADGCLQLFGGYGYTTEYPISRAFIDARVQRI 363

Query: 406 GAGTSEVRRLVIGRA 420
             GTSEV + +I R+
Sbjct: 364 YGGTSEVMKEIIARS 378


Lambda     K      H
   0.321    0.137    0.410 

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: 377
Number of extensions: 20
Number of successful extensions: 3
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: 426
Length of database: 383
Length adjustment: 31
Effective length of query: 395
Effective length of database: 352
Effective search space:   139040
Effective search space used:   139040
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: 50 (23.9 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