GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Methylocystis bryophila S285

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_085772524.1 B1812_RS16285 isovaleryl-CoA dehydrogenase

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_002117405.1:WP_085772524.1
          Length = 389

 Score =  197 bits (502), Expect = 3e-55
 Identities = 122/375 (32%), Positives = 197/375 (52%), Gaps = 2/375 (0%)

Query: 14  LDQQLADDERMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQYG 73
           +D  L D+   +R +   +A  ++APR        +  + ++R+MG +GLLG ++PE+YG
Sbjct: 8   MDFGLGDEGETLRRSVAEFASREIAPRAARIDADNSFPSDLWRKMGSMGLLGVSVPEEYG 67

Query: 74  GPGLDYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEWI 133
           G  L Y+++ +   EV R  +         S+L +  I   G  AQK +YLPKL +GE +
Sbjct: 68  GVALGYLAHVVAMEEVSRASASVGLSYGAHSNLCVNQIQRNGGRAQKLRYLPKLISGEHV 127

Query: 134 GCFGLTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIADVFVVWAKLDED-GRDE 192
           G   ++EP  GSD  +M  RA +    Y L+G KMW+TN P AD+ +V+AK   + G   
Sbjct: 128 GALAMSEPAAGSDVVNMRMRAERRGDRYVLNGDKMWVTNGPDADIVIVYAKTSPNAGAHG 187

Query: 193 IRGFILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEENILPHVK-GLRGPFTCLN 251
           I  FI+E G KGL       K+G+R S T ++  ++  VP +NIL     G+    + L+
Sbjct: 188 ITAFIVEGGFKGLRRMPKLDKLGMRGSNTCQLFFEDCEVPVDNILGEPDCGINVLMSGLD 247

Query: 252 SARYGIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQGVL 311
             R  +A G +G   +C  +   Y+ DRKQFGR +   +++Q KLADM T ++     V 
Sbjct: 248 YERVILAGGPIGIMRACLDVVLPYMHDRKQFGRSIGEFEIMQGKLADMYTALSATRAYVY 307

Query: 312 RLGRMKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVVN 371
            + R  D G  + +  +     +  +A  +A  A   LGGNG  +++   R L + ++  
Sbjct: 308 AVARACDAGCVSRKDAAGAILFAAERATQMALQAIQCLGGNGYMNDYPTGRLLRDAKLYE 367

Query: 372 TYEGTHDIHALILGR 386
              GT +I  +++GR
Sbjct: 368 IGAGTSEIRRMLIGR 382


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: 377
Number of extensions: 20
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: 389
Length adjustment: 31
Effective length of query: 364
Effective length of database: 358
Effective search space:   130312
Effective search space used:   130312
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