GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Croceitalea dokdonensis DOKDO 023

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_054558672.1 I595_RS04620 acyl-CoA dehydrogenase

Query= reanno::ANA3:7024494
         (389 letters)



>NCBI__GCF_001306415.1:WP_054558672.1
          Length = 380

 Score =  281 bits (720), Expect = 2e-80
 Identities = 153/377 (40%), Positives = 226/377 (59%)

Query: 8   LNFGLGEEVDMLRDAVQDFAKHEIAPIAAKVDHDNAFPNEIWPVLGGMGLLGVTVPEEYG 67
           ++F L EE  M++ A +DFA++E+ P   + D   AFP E    +  +G +G+ V  +YG
Sbjct: 1   MDFTLTEEQQMVQQAAKDFAQNELLPGIIERDDAQAFPKEQVKKMAELGFMGMMVDSKYG 60

Query: 68  GANMGYLAHVVAMEEISRASASIGLSYGAHSNLCVNQINRNGNAEQKAKYLPKLVSGEHI 127
           G+ +  L++V+ MEE+S+  AS  +    +++L    +   G   QK KYL +L +GE I
Sbjct: 61  GSGLDTLSYVLVMEELSKIDASSSVIVSVNNSLVCWGLETFGTEAQKEKYLSRLATGEII 120

Query: 128 GALAMSEPNAGSDVVSMKLHARKEGDRYILNGNKMWITNGPDANTYVIYAKTDLTKGAHG 187
           GA  +SEP AGSD  S K  A  +GD Y++NG K WITNG  A  Y++ A+TD+ KG  G
Sbjct: 121 GAFCLSEPEAGSDATSQKTTAIDKGDHYLINGTKNWITNGNSAEVYLVIAQTDVEKGHKG 180

Query: 188 ITAFIVERGFKGFSQAQKLDKLGMRGSNTCELVFEDVEVPEENILGGLNNGVKVLMSGLD 247
           I A IVE+G  GF    K +K+G+R S+T  L+F DV+VP+EN +G    G K  M  L 
Sbjct: 181 INALIVEKGTDGFEIGPKENKMGIRSSDTHSLLFNDVKVPKENRIGEDGFGFKFAMKTLA 240

Query: 248 YERVVLSGGPLGIMNACMDIVVPYIHEREQFGKSIGEFQLVQGKLADMYTGMNAAKAYVY 307
             R+ ++   LGI     ++ + Y  ER+ FG  I   Q +  KLADM+T + AA+  VY
Sbjct: 241 GGRIGIAAQALGIAAGAYELALKYSKERKAFGTEICNHQAIAFKLADMHTKIQAARHLVY 300

Query: 308 SVAKSCDRGETTRKDAAGAILYSAELATKMALDAIQLLGGNGYVNEYATGRLLRDAKLYE 367
             A   D G+      A A LY+AE A ++A +A+Q+ GGNG+V +Y   RL+RDAK+ +
Sbjct: 301 QAAWDKDNGKDYTLSGAMAKLYAAETAMEVATEAVQIHGGNGFVKDYHVERLMRDAKITQ 360

Query: 368 IGAGTSEIRRMLIGREL 384
           I  GTSEI++++I R +
Sbjct: 361 IYEGTSEIQKIVISRSI 377


Lambda     K      H
   0.316    0.135    0.388 

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: 380
Number of extensions: 17
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: 389
Length of database: 380
Length adjustment: 30
Effective length of query: 359
Effective length of database: 350
Effective search space:   125650
Effective search space used:   125650
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 (21.6 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