GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Sphingomonas histidinilytica UM2

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_079650004.1 B5X82_RS20375 acyl-CoA dehydrogenase

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_900167915.1:WP_079650004.1
          Length = 393

 Score =  130 bits (328), Expect = 5e-35
 Identities = 103/337 (30%), Positives = 150/337 (44%), Gaps = 12/337 (3%)

Query: 58  MGEIGLLGPTIPEQYGGPGLDY-VSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGS 116
           +G+   L  T+P  +GG      V    ++R++    SG    +     L    I  FGS
Sbjct: 52  LGQADFLRATVPSNHGGLNSPVDVRTLCLSRQILAYHSGLADFVFAMQGLGTGAISLFGS 111

Query: 117 DAQKEKYLPKLATGEWIGCFGLTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIA 176
           +A K+ YLPK+A GE I  F L+E   GSD  +M T AR+V GG+ + G K WI+N  IA
Sbjct: 112 EAIKQAYLPKVAAGEMIAGFALSEKEAGSDVAAMTTSARRVEGGWIIDGEKTWISNGTIA 171

Query: 177 DVFVVWAKLDE-DGRDEIRGFILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEEN 235
           D+  V+A+  E  G   I  F      KG S       +      T  I  DE FVP+++
Sbjct: 172 DLLTVFARSGEAPGARGISAFAFPTATKGFSITERIDVIAPHPLAT--IRFDECFVPDDH 229

Query: 236 ILPHV-KGLRGPFTCLNSARYGIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQK 294
           +L    +G +     L+  R  +   ALG A      A      R+ FG PL+  QL Q 
Sbjct: 230 LLGEAGQGFKVAMATLDMLRSTVGAAALGFARRATDEALGRATSRELFGAPLSDLQLTQA 289

Query: 295 KLADMQTEITLGLQGVLRLGRMKDEGTAAVEITSIMKRNSCGKALDIARLARD----MLG 350
            LADM          + R    KD+G   +   + M +     A D A+L  D    + G
Sbjct: 290 ALADMALGNDSSALLIYRAAWAKDQGQPRITREAAMAKL---HATDTAQLTIDKAVQLFG 346

Query: 351 GNGISDEFGVARHLVNLEVVNTYEGTHDIHALILGRA 387
           G G+     V R    +  +  YEG  ++  +++ RA
Sbjct: 347 GAGVVRGNMVERLYREIRALRIYEGASEVQKVVIARA 383


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: 341
Number of extensions: 21
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: 393
Length adjustment: 31
Effective length of query: 364
Effective length of database: 362
Effective search space:   131768
Effective search space used:   131768
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