GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Dyella japonica UNC79MFTsu3.2

Align 2-methylbutanoyl-CoA dehydrogenase / butanoyl-CoA dehydrogenase / isobutyryl-CoA dehydrogenase (EC 1.3.8.1; EC 1.3.8.5) (characterized)
to candidate N515DRAFT_0484 N515DRAFT_0484 glutaryl-CoA dehydrogenase

Query= reanno::pseudo3_N2E3:AO353_25680
         (375 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0484
          Length = 389

 Score =  230 bits (586), Expect = 6e-65
 Identities = 131/374 (35%), Positives = 202/374 (54%), Gaps = 6/374 (1%)

Query: 2   LPTDEQLQISDAARQFAQERLKPFAAEWDREHRFPKEAIGEMAELGFFGMLVPEQWGGCD 61
           L TDE+  + D   +F  ER+ P   +   + RFPKE I E+A LG  G  +PEQ+G   
Sbjct: 16  LLTDEERMVQDTVGRFVDERVLPIIGDAFDQGRFPKELIPEIAGLGLLGATLPEQYGCAG 75

Query: 62  TGYLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILKFGNDDQKERFLKPLASGAMLGAF 121
              ++Y +  +E+  GD    +  SV +S+   PI  +G ++QK  +L  +A+G ++G F
Sbjct: 76  MNGVSYGLICQELERGDSGLRSFASVQSSLCMYPIYAYGTEEQKLHYLPKMAAGEIIGCF 135

Query: 122 ALTEPQAGSDASSLKTRARLNGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISA 181
            LTEP  GSD +++KT AR +G  +++NG K +IT+G  A + IV+A T+      GI  
Sbjct: 136 GLTEPHGGSDPANMKTNARKDGGDWIINGAKMWITNGNLAHIAIVWAQTED-----GIQG 190

Query: 182 FIVPTDSPGYKVARVEDKLGQHASDTCQILFEDVQVPVANRLGEEGEGYKIALANLEGGR 241
           FIVPTDS G+    V  K+   AS T  + F+ V+VP ANRL    +G K  L  L   R
Sbjct: 191 FIVPTDSQGFTAQEVHKKMSLRASVTSALFFDSVRVPEANRL-PNVKGLKGPLGCLTQAR 249

Query: 242 VGIASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAA 301
            GI    +G A+A  +   DY +ER  FG+P+  +QA+  +LA+MA +I +A+ +     
Sbjct: 250 YGITWGPIGAAQACLKEVLDYTQERVLFGRPLASNQAIQLKLAEMARRITMAQLLSLQLG 309

Query: 302 ALRDSGKPALVEASMAKLFASEMAEKVCSTALQTLGGYGYLSDFPLERIYRDVRVCQIYE 361
            L+D+G     + S+AK     +A  +       LGG G  ++    R   ++     YE
Sbjct: 310 RLKDAGNMQPTQVSLAKWNNCRIAIDIARECRDILGGAGITTEHVAIRHALNLESVITYE 369

Query: 362 GTSDIQRMVISRNL 375
           GT  + ++V+ R L
Sbjct: 370 GTETVHQLVVGREL 383


Lambda     K      H
   0.319    0.134    0.389 

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: 333
Number of extensions: 15
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: 375
Length of database: 389
Length adjustment: 30
Effective length of query: 345
Effective length of database: 359
Effective search space:   123855
Effective search space used:   123855
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 Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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