GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Acidovorax caeni R-24608

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_054256957.1 BN2503_RS12310 acyl-CoA dehydrogenase

Query= reanno::Smeli:SM_b21121
         (387 letters)



>NCBI__GCF_001298675.1:WP_054256957.1
          Length = 392

 Score =  244 bits (623), Expect = 3e-69
 Identities = 144/377 (38%), Positives = 211/377 (55%), Gaps = 8/377 (2%)

Query: 13  EIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHGGAGLGYL 72
           E+    AS+ RF    I P   D +++      L+R+MGE G L     E +GGAG    
Sbjct: 14  ELQVFTASLERFCDTEIEPHYRDWEKAGLVSRELFRKMGENGYLCADVPEPYGGAGASVH 73

Query: 73  AHCVAMEEISRASASVGLSYG--AHSNLCVNQINRNGKPAQKSRYLPKLISGEHVGALAM 130
                +E +SR     G   G   H+++    +   G  AQ+  +LP+++SGE V A+ M
Sbjct: 74  FSFAVVEVLSRRGYG-GFVGGLQVHNDIIPPYLLHCGTEAQRQYWLPRMVSGEAVAAIGM 132

Query: 131 SEPGAGSDVVSMKLKA----DKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRGI 186
           +EPGAGSD+ +++  A    D  GD YV+NGSK++I+NG   D+LV+ AKTDPAAG +G+
Sbjct: 133 TEPGAGSDLKAIRTTARRISDSDGDGYVINGSKIFISNGQHCDLLVLAAKTDPAAGAKGV 192

Query: 187 TAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGV-GEGVKVLMSGLD 245
           + FLV+   PGF+ GQ L+K+G    +TSEL F D  VP++ +LGGV G+G   +M  L 
Sbjct: 193 SLFLVDTKSPGFTRGQNLEKIGQHAGDTSELFFNDLRVPQDALLGGVEGQGFVQMMRELP 252

Query: 246 YERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVY 305
            ER+++    +      LD  V Y+ ER+ FGQ IG+FQ  +  LA     + AA+A++ 
Sbjct: 253 RERLIIGVQAVYGAKGALDATVKYVQERQAFGQAIGQFQNTRFTLAQCASDIAAAKAFLN 312

Query: 306 AVAAACDRGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLYE 365
           A  AA +RGE   +  +   L+  E    +A   +Q  GG GY  +YP  R   DA++  
Sbjct: 313 ASVAAYERGELTPEAVSALKLHTTEVFGRVADACLQLFGGYGYMAEYPISRFWTDARVLR 372

Query: 366 IGAGTSEIRRMLIGREL 382
           I  GTSEI + L+ R L
Sbjct: 373 IYGGTSEIMKELVARSL 389


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: 329
Number of extensions: 12
Number of successful extensions: 4
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: 392
Length adjustment: 30
Effective length of query: 357
Effective length of database: 362
Effective search space:   129234
Effective search space used:   129234
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