GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Hippea alviniae EP5-r

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_022669656.1 G415_RS0100700 acyl-CoA dehydrogenase family protein

Query= reanno::Phaeo:GFF1011
         (386 letters)



>NCBI__GCF_000420385.1:WP_022669656.1
          Length = 379

 Score =  213 bits (543), Expect = 6e-60
 Identities = 124/374 (33%), Positives = 199/374 (53%), Gaps = 4/374 (1%)

Query: 8   FDLGEDVNALRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITVPEEFGGA 67
           F   E+    R  V  + +++++P  +E+++K     E+ + + +  L GI +P+E+ G 
Sbjct: 4   FTFTEEQEIFRKKVAEFTEKKIKPKVREMEEKKVALPEVVEALKDEKLTGIFIPKEYNGL 63

Query: 68  GMSYLAHTVAVEEIARASASVSLSYGAHSNLCVNQIKLNGNAEQKAKYLPRLVSGEHVGA 127
           G+ Y    +A+EEIA+ S  V++       L +  I   GN EQK KYLP L  GE +  
Sbjct: 64  GLGYTERLIALEEIAKVSPGVAMMLQIFG-LGIEPILKFGNDEQKQKYLPGLAVGEKLAT 122

Query: 128 LAMSEAGAGSDVVSMSLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDPDAGSKGMT 187
           +A++EA  GSD   +    +K  D Y LNG K  +TN P A+T VV AK   +   K  +
Sbjct: 123 VAVTEATGGSDPTGIKTTYKKEGDFYILNGRKIMLTNAPIANTFVVLAKDSENP--KAFS 180

Query: 188 AFLIEKEFKGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVLGEEGKGVRVLMSGL-DY 246
             +IE  F+GF   + + ++G+ G +  E++ E+ +VP  N+LG+EGKG+RV MS + + 
Sbjct: 181 TLIIEDTFEGFRRGKEWHEIGLHGCSVGEILLENCKVPASNLLGQEGKGMRVAMSAIGEV 240

Query: 247 ERVVLAGIGTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTARAYVYE 306
            R  + G+  GIM   +   + + K+R  +G+PI N Q +Q KIA+M   +   R   Y 
Sbjct: 241 GRGGMVGVALGIMDTLLKITVNFSKKRILYGKPISNLQTIQNKIAEMRLDLEIGRLLGYR 300

Query: 307 VAKACDKGTVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRDAKLMEI 366
                DKG  +  + A    + +E A   A  AV   GG G   +  V R  RD+ ++  
Sbjct: 301 ATSIQDKGQRSDLEFAMAKYFTTEAAQKAAKMAVDIQGGYGVTEEAVVTRFLRDSFVLGP 360

Query: 367 GAGTSEIRRMLIGR 380
            AGTS+I +++I R
Sbjct: 361 SAGTSDIMKVIIAR 374


Lambda     K      H
   0.318    0.132    0.382 

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: 348
Number of extensions: 21
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: 386
Length of database: 379
Length adjustment: 30
Effective length of query: 356
Effective length of database: 349
Effective search space:   124244
Effective search space used:   124244
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 Apr 09 2024. 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