GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Sphingomonas indica Dd16

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_085218433.1 B9N75_RS08665 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF1051
         (387 letters)



>NCBI__GCF_900177405.1:WP_085218433.1
          Length = 380

 Score =  260 bits (664), Expect = 5e-74
 Identities = 142/367 (38%), Positives = 216/367 (58%), Gaps = 2/367 (0%)

Query: 16  MLREQVQAFVAAEIAPRAEAIDQENLFPADMWRKFGEMGLLGVTVSEEYGGAGLGYLAHV 75
           + R+QV+ F    + P  +  ++E +   D+W + GE GLL  TV EEYGG GL +  + 
Sbjct: 16  LFRDQVRRFFDKALIPHLDRWEEEGIVDRDLWTQCGETGLLCPTVPEEYGGLGLDFRYNA 75

Query: 76  VAMEEISRGSASVALSYGAHSNLCVNQINRNGNPEQKARYLPKLISGEHVGALAMSEPNA 135
           V  EE++   ++  ++   HS++  + I   G+  QK  +LP++ISGE   A+AM+EP A
Sbjct: 76  VIDEELAYAGSTAGITL--HSDIVADYIVVYGSEAQKQHWLPRMISGETPTAIAMTEPGA 133

Query: 136 GSDVVSMKLRAEKRGDRYVLNGSKTWITNGPDANTYVIYAKTDLDKGAHGITAFIVERDW 195
           GSD+  ++  A + GD YV+NGSKT+ITNG  A+  ++ AKTD  +GA G +  +VE D 
Sbjct: 134 GSDLQGVRTTAIRDGDSYVINGSKTYITNGQHADLVIVVAKTDPSQGAKGTSLILVEADR 193

Query: 196 KGFSRGNKFDKLGMRGSNTCELFFDDVEVPQENVLGAENGGVKVLMSGLDYERVVLAGGP 255
           +GF+RG   DK+G+   +T E+FF+DV VP +N+LG E  G   LM+ L  ER+ +A   
Sbjct: 194 EGFARGRNLDKIGLHSQDTSEMFFNDVRVPADNLLGQEGAGFAYLMNQLPQERLSIACSA 253

Query: 256 TGIMQSCLDVVVPYIHDRKQFGQSIGEFQFIQGKVADMYTQLNASRAYLYAVAQACDRGE 315
            G  Q   D  + +  DRK FG+S+ +FQ  +  +AD+ T+L    A+L         GE
Sbjct: 254 QGAAQRAFDEALAFTRDRKAFGKSVLDFQNTRFTLADLATKLQVGWAHLDWAITRHVAGE 313

Query: 316 TTRKDAAGVILYTAENATQMALQAIQILGGNGYINEFPTGRLLRDAKLYEIGAGTSEIRR 375
            T  +A+   L+  E   +    A+Q+ GG GY+NE+   RL RDA++  I  GT+EI +
Sbjct: 314 LTATEASAAKLWHTELQGEACDTALQLHGGAGYMNEYLIARLWRDARVTRIFGGTNEIMK 373

Query: 376 MLIGREL 382
            +IGR L
Sbjct: 374 EVIGRGL 380


Lambda     K      H
   0.318    0.135    0.391 

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: 399
Number of extensions: 23
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: 387
Length of database: 380
Length adjustment: 30
Effective length of query: 357
Effective length of database: 350
Effective search space:   124950
Effective search space used:   124950
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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