GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Acidovorax caeni R-24608

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_054254922.1 BN2503_RS01730 acyl-CoA dehydrogenase

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_001298675.1:WP_054254922.1
          Length = 596

 Score = 95.1 bits (235), Expect = 5e-24
 Identities = 98/374 (26%), Positives = 162/374 (43%), Gaps = 55/374 (14%)

Query: 55  FREMGEIGLLGPTIPEQYGGPGLDYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEF 114
           +R+  E G  G   P  +GG GL           +   +  + ++  + +   +  +   
Sbjct: 81  YRQFAEGGWQGLQHPTDFGGQGLPKTIGAACGEMINSANLSF-ALCPLLTDGAIEALLTA 139

Query: 115 GSDAQKEKYLPKLATGEWIGCFGLTEPNHGSDPGSMVTRARKVPGG-YSLSGSKMWIT-- 171
           GSDA K  YL KL +GEW G   LTEP  GSD   + T+A   P G Y + G+K++IT  
Sbjct: 140 GSDALKATYLEKLISGEWTGTMNLTEPQAGSDLSLVRTKAEPQPDGTYKIFGTKIFITYG 199

Query: 172 NSPIAD--VFVVWAKL--DEDGRDEIRGFILEKGCKGLSAP----------AIHGKVGLR 217
              +AD  V +V A++    +G   I  F++ K   G              +I  K+G++
Sbjct: 200 EHDMADNIVHLVLARVVGAPEGVKGISLFVVPKFMVGADGSLGARNDVHCVSIEHKLGIK 259

Query: 218 ASITGEIVLDEA------FVPEENILPHVKGLRGPFTCLNSARYGIAWGALGAAESCWHI 271
           AS T  +   +        V EEN     +GL   F  +N+ARYG+    +  AE  +  
Sbjct: 260 ASPTAVLQFGDHGGAIGYLVGEEN-----RGLEYMFIMMNAARYGVGVQGIAVAERAYQQ 314

Query: 272 ARQYVLDRKQFGRPLAANQL----------IQKKLADMQTEITLGLQGVLRLG------- 314
           A QY  DR Q  RP+  +            +++ L  M+   T G + +  +        
Sbjct: 315 AVQYARDRVQ-SRPVDGSVAGAAAIIHHPDVRRMLMTMRA-YTEGCRAMASVAAAAYDAA 372

Query: 315 ------RMKDEGTAAVE-ITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNL 367
                 +++ +  A  E +  ++K  S   + ++  L   + GG G  +E G A+H  + 
Sbjct: 373 HHHPDAQVRSDNAAFYEFMVPLVKGYSTEMSQEVTSLGVQVHGGMGFIEETGAAQHYRDS 432

Query: 368 EVVNTYEGTHDIHA 381
           +++  YEGT  I A
Sbjct: 433 KILTIYEGTTAIQA 446


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: 493
Number of extensions: 20
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 395
Length of database: 596
Length adjustment: 34
Effective length of query: 361
Effective length of database: 562
Effective search space:   202882
Effective search space used:   202882
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: 52 (24.6 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