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_028310770.1 H566_RS0106285 acyl-CoA dehydrogenase

Query= BRENDA::B0EVL5
         (395 letters)



>NCBI__GCF_000482785.1:WP_028310770.1
          Length = 600

 Score = 85.1 bits (209), Expect = 5e-21
 Identities = 101/378 (26%), Positives = 157/378 (41%), Gaps = 62/378 (16%)

Query: 57  FNEMGELGLLGATIPEQYGGSGMNYVCYGLIAREVERVDSGYRS--MMSVQSSLVMVPIN 114
           F +  E G  G   P +YGG GM  +   L +  +E V+S   S  +  + +   +  + 
Sbjct: 81  FKQFVEGGWQGVLHPAEYGGMGMPKL---LASPCIEMVNSASLSFALCPLLTDGAIEALL 137

Query: 115 EFGSEETKQKYLPKLATGEWVGCFGLTEPNHGSDPGSMVTRA-RKVDGGYSLSGAKMWIT 173
             GS+  KQ Y+  +  G W G   LTEP  GSD   + TRA  + DG Y +SG K++IT
Sbjct: 138 TAGSDTMKQTYIGPMIEGRWTGTMNLTEPGAGSDLAQVRTRAVPQGDGTYRISGQKIFIT 197

Query: 174 NSP------IADVFVVWAKDDAGDIRG---FVLEK------GWKG----LSAPAIHGKVG 214
                    I  + +    D    ++G   FV+ K      G  G    +   +I  K+G
Sbjct: 198 YGEHDFAENIVHLVLARLPDAPEGVKGISLFVVPKFLVNDDGSLGKRNDVWCASIEHKLG 257

Query: 215 LRASITGEIVMDE-----------VFCPEENAFPTVRGLKGPFTCLNSARYGIAWGALGA 263
           ++AS T  ++  +               EEN     RGL+  F  +NSAR+G+    +  
Sbjct: 258 IKASPTAVLLFGDDKGEVGAGGIGYLVGEEN-----RGLEYMFVMMNSARFGVGMQGIAV 312

Query: 264 AEACYETARQYTMDRKQF------GRPLA-ANQLIQKKLADMLTEITLGLQGCLRLGRLK 316
           AE  Y+ A QY  DR Q         P+A  N    K+L   +   T G +    +   +
Sbjct: 313 AERAYQKAVQYAKDRVQSRDLTGGKEPVAIINHPDVKRLLMNMRAQTEGARALAYVAAAR 372

Query: 317 DE-----------GNAPVE---LTSIMKRNSCGKSLDIARVARDMLGGNGISDEFCIARH 362
            +             A  E   L  ++K  S   S+ +A     + GG G  +E   A++
Sbjct: 373 YDVAHHSPDAEAAAQAQAEYEFLVPVVKGWSTEMSIQVASDGVQVHGGMGFIEETGAAQY 432

Query: 363 LVNLEVVNTYEGTHDIHA 380
             +  ++  YEGT  I A
Sbjct: 433 YRDARILTIYEGTTAIQA 450


Lambda     K      H
   0.319    0.136    0.409 

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: 513
Number of extensions: 24
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: 600
Length adjustment: 34
Effective length of query: 361
Effective length of database: 566
Effective search space:   204326
Effective search space used:   204326
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 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