GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Brevibacterium jeotgali SJ5-8

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_101586889.1 BJEO58_RS00850 acyl-CoA dehydrogenase

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_900169175.1:WP_101586889.1
          Length = 390

 Score =  171 bits (432), Expect = 4e-47
 Identities = 114/378 (30%), Positives = 178/378 (47%), Gaps = 9/378 (2%)

Query: 18  LADDERMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQYGGPGL 77
           L ++   +R     +  G++AP   +         A+  +MG++GL G   PE+YGG G 
Sbjct: 9   LPEEYETLRRTVATFTDGEVAPVSAQLDAKHEFPYALVEQMGDMGLFGLPFPEEYGGMGG 68

Query: 78  DYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEWIGCFG 137
           DY +  L   E+ R +      +    SL  +PIF FG+DAQK++ LP +  G  +  FG
Sbjct: 69  DYFALCLALEEIARENQSLAMTLEAGVSLGAMPIFRFGTDAQKQELLPHVIDGRGLAAFG 128

Query: 138 LTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSP------IADVFVVWAKLDEDG-- 189
           LTE   GSD G   T+A    G + ++GSK +ITNS       +    V   +   DG  
Sbjct: 129 LTEAEAGSDAGGTKTKAVLENGEWVVNGSKSFITNSGTDITKFVTATAVTGTRTGSDGSR 188

Query: 190 RDEIRGFILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEENIL-PHVKGLRGPFT 248
           + EI   I+  G  G +    + KVG  +S T  +  D   VPE N+L    +G      
Sbjct: 189 KPEISTIIVPNGTPGFTPEPAYDKVGWNSSDTHPLTFDGVRVPEANLLGERGRGYANFLR 248

Query: 249 CLNSARYGIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQ 308
            L+  R  IA  ++GAA+ C   + QY  +R  FG+P+   Q I  K+A M+  +     
Sbjct: 249 ILDEGRIAIAAVSVGAAQGCVDASVQYAKERTAFGKPIGDYQGISFKIARMEARVQSARA 308

Query: 309 GVLRLGRMKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLE 368
                    + G    +  +I K  +   A+D AR A  + GG G  +E  VARH  + +
Sbjct: 309 AYYAAASKMESGLPFKKEAAIAKMVASEAAMDNARDATQVHGGYGFMNESLVARHYRDSK 368

Query: 369 VVNTYEGTHDIHALILGR 386
           ++   EGT ++  +++ R
Sbjct: 369 ILEIGEGTTEVQLMLIAR 386


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: 430
Number of extensions: 25
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: 395
Length of database: 390
Length adjustment: 31
Effective length of query: 364
Effective length of database: 359
Effective search space:   130676
Effective search space used:   130676
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 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