GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Rhizobium leguminosarum bv. trifolii WSM1325

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate WP_012760746.1 RLEG_RS35160 isovaleryl-CoA dehydrogenase

Query= BRENDA::Q3JP94
         (395 letters)



>NCBI__GCF_000023185.1:WP_012760746.1
          Length = 381

 Score =  194 bits (494), Expect = 3e-54
 Identities = 124/376 (32%), Positives = 190/376 (50%), Gaps = 2/376 (0%)

Query: 13  LLDQQLADDERMVRDAAHAYAQGKLAPRVTEAFRHETTDAAIFREMGEIGLLGPTIPEQY 72
           + D  L +    +R+    +A   +AP   E     T    ++ EMG +GL G T+ E++
Sbjct: 1   MFDFSLGETADAIRETTARFAADHIAPLAVEIDESNTFPRQLWPEMGALGLHGITVEEEF 60

Query: 73  GGPGLDYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIFEFGSDAQKEKYLPKLATGEW 132
           GG GL Y+ + +   EV R  +         S+L +  I  + S  QK +YLPKL +GE 
Sbjct: 61  GGAGLGYLDHVVAMEEVSRASASVGLSYGAHSNLCVNQIRRWASPEQKRRYLPKLISGEH 120

Query: 133 IGCFGLTEPNHGSDPGSMVTRARKVPGGYSLSGSKMWITNSPIADVFVVWAKLD-EDGRD 191
           +G   ++E   GSD  SM  RA K    Y L+G+K WITN+P ADV VV+AK D   G  
Sbjct: 121 VGSLAMSEVGAGSDVVSMRLRAEKKGDRYVLNGTKFWITNAPHADVLVVYAKTDPAAGPK 180

Query: 192 EIRGFILEKGCKGLSAPAIHGKVGLRASITGEIVLDEAFVPEENILPHV-KGLRGPFTCL 250
            I   I+EKG  G        K+G+R S T E+V ++  VP E ++    +G++   + L
Sbjct: 181 GISALIIEKGLPGFGVSKKLSKLGMRGSDTAELVFEDCAVPAEALMGREGEGVKILMSGL 240

Query: 251 NSARYGIAWGALGAAESCWHIARQYVLDRKQFGRPLAANQLIQKKLADMQTEITLGLQGV 310
           +  R  +A G LG  ++C  +   YV DRKQFG+ +   QL+Q K+ADM   +      V
Sbjct: 241 DYERAVLAGGPLGIMQACLDVVLPYVRDRKQFGKAIGDFQLMQGKIADMYVALNSARAYV 300

Query: 311 LRLGRMKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVV 370
             + R  D G A     +     +   A+ ++  A   LGG G + E+ V R L + ++ 
Sbjct: 301 YSVARACDAGRATRTDAAAAILFASENAVKVSLEAIQALGGAGYTKEWPVERFLRDAKLY 360

Query: 371 NTYEGTHDIHALILGR 386
           +   GT++I   ++GR
Sbjct: 361 DIGAGTNEIRRYLIGR 376


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: 353
Number of extensions: 19
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: 381
Length adjustment: 30
Effective length of query: 365
Effective length of database: 351
Effective search space:   128115
Effective search space used:   128115
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