GapMind for catabolism of small carbon sources

 

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

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_022669656.1 G415_RS0100700 acyl-CoA dehydrogenase family protein

Query= reanno::pseudo6_N2E2:Pf6N2E2_1146
         (375 letters)



>NCBI__GCF_000420385.1:WP_022669656.1
          Length = 379

 Score =  214 bits (544), Expect = 4e-60
 Identities = 122/371 (32%), Positives = 200/371 (53%), Gaps = 4/371 (1%)

Query: 4   TEEQTQIRDMARQFAEERLKPFAAEWDREHRFPREAIDEMAELGFFGMLVPEQWGGCDTG 63
           TEEQ   R    +F E+++KP   E + +     E ++ + +    G+ +P+++ G   G
Sbjct: 7   TEEQEIFRKKVAEFTEKKIKPKVREMEEKKVALPEVVEALKDEKLTGIFIPKEYNGLGLG 66

Query: 64  YLAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKFGNDEQKAKFLTPLASGAMLGAFAL 123
           Y    + LEEIA      + ++ +   +G  PILKFGNDEQK K+L  LA G  L   A+
Sbjct: 67  YTERLIALEEIAKVSPGVAMMLQIFG-LGIEPILKFGNDEQKQKYLPGLAVGEKLATVAV 125

Query: 124 TEPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           TE   GSD + +KT  + EGD Y+LNG K  +T+   A   +V A    S   +  S  I
Sbjct: 126 TEATGGSDPTGIKTTYKKEGDFYILNGRKIMLTNAPIANTFVVLA--KDSENPKAFSTLI 183

Query: 184 VPTDSPGYSVARVEDKLGQHASDTCQILFEDLKVPVGNRLGEEGEGYKIALANL-EGGRV 242
           +     G+   +   ++G H     +IL E+ KVP  N LG+EG+G ++A++ + E GR 
Sbjct: 184 IEDTFEGFRRGKEWHEIGLHGCSVGEILLENCKVPASNLLGQEGKGMRVAMSAIGEVGRG 243

Query: 243 GIAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAA 302
           G+   A+G+     +   +++++R  +GKPI   Q +  ++A+M   + + R + + A +
Sbjct: 244 GMVGVALGIMDTLLKITVNFSKKRILYGKPISNLQTIQNKIAEMRLDLEIGRLLGYRATS 303

Query: 303 LRDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYEG 362
           ++D GQ + +E +MAK F +E A+K   MA+   GGYG   +  + R  RD  V     G
Sbjct: 304 IQDKGQRSDLEFAMAKYFTTEAAQKAAKMAVDIQGGYGVTEEAVVTRFLRDSFVLGPSAG 363

Query: 363 TSDIQRMVISR 373
           TSDI +++I+R
Sbjct: 364 TSDIMKVIIAR 374


Lambda     K      H
   0.320    0.134    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: 316
Number of extensions: 20
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: 375
Length of database: 379
Length adjustment: 30
Effective length of query: 345
Effective length of database: 349
Effective search space:   120405
Effective search space used:   120405
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 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