GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Derxia gummosa DSM 723

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_028312898.1 H566_RS0120480 acyl-CoA dehydrogenase family protein

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_000482785.1:WP_028312898.1
          Length = 383

 Score =  214 bits (546), Expect = 3e-60
 Identities = 129/374 (34%), Positives = 198/374 (52%), Gaps = 2/374 (0%)

Query: 15  DQQLADDERMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQYGG 74
           D +L D++RMVRD A  +A+ ++APR     R    D      MG +GLLG  +PE +GG
Sbjct: 3   DIELTDEQRMVRDMARDFARNEVAPRAEAWERDGWIDGNTVARMGGLGLLGMVVPEHWGG 62

Query: 75  PGLDYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEWIG 134
            G DYVSY L   E+   D    ++MS+ +S+   P+   G+D Q+  +LP+LA GE IG
Sbjct: 63  AGTDYVSYALAVEEISAGDGALGALMSIHNSVGCGPLLAHGNDEQRRAWLPQLARGEAIG 122

Query: 135 CFGLTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIADVFVVWAKLD-EDGRDEI 193
           CF LTEP  GS+  ++ TRA    G + + G+K +++N+  A + +V+A  D E G+  +
Sbjct: 123 CFCLTEPQAGSEAHNLRTRAVLRNGDWVIDGAKQFVSNAKRAKLAIVFAVTDPELGKKGL 182

Query: 194 RGFILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEENIL-PHVKGLRGPFTCLNS 252
             F++     G +   +  K+G+RAS T  + LD   VP  N+L    +GL    + L  
Sbjct: 183 SAFLVPTDTPGFAIQRVEHKMGIRASDTCAVALDGVRVPAANLLGERNRGLSIALSNLEG 242

Query: 253 ARYGIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQGVLR 312
            R GI   ALG A + +  A +Y  +R QFGRP+  +  I +KLADM+ +I      VL 
Sbjct: 243 GRIGIGAQALGIARAAFEAALRYSRERVQFGRPIHEHAPIAEKLADMKVQINAARLLVLH 302

Query: 313 LGRMKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVVNT 372
             R+K  G   +   S  K  +   A  +   A  + GG G   ++ V R+  +  +   
Sbjct: 303 AARLKQAGLPCLSEASQAKLFASEMAERVCSAAVQIHGGYGYLADYAVERYYRDARITQI 362

Query: 373 YEGTHDIHALILGR 386
           YEGT +I  +++ R
Sbjct: 363 YEGTSEIQRMLIAR 376


Lambda     K      H
   0.320    0.138    0.414 

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: 399
Number of extensions: 16
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: 395
Length of database: 383
Length adjustment: 30
Effective length of query: 365
Effective length of database: 353
Effective search space:   128845
Effective search space used:   128845
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