GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Rhizobium leguminosarum 3841

Align furfuryl alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate WP_041936742.1 RL_RS26020 alcohol dehydrogenase AdhP

Query= metacyc::MONOMER-17184
         (342 letters)



>NCBI__GCF_000009265.1:WP_041936742.1
          Length = 360

 Score =  456 bits (1172), Expect = e-133
 Identities = 221/339 (65%), Positives = 264/339 (77%), Gaps = 1/339 (0%)

Query: 4   MMKAAVVRAFGAPLTIDEVPVPQPGPGQVQVKIEASGVCHTDLHAADGDWPVKPTLPFIP 63
           +MKAAVVR FG PL I+ VPVP PGPG++ VK+ A GVCHTDLHAADGDWPVKPT PFIP
Sbjct: 8   LMKAAVVREFGKPLAIECVPVPVPGPGEILVKVVACGVCHTDLHAADGDWPVKPTPPFIP 67

Query: 64  GHEGVGYVSAVGSGVSRVKEGDRVGVPWLYSACGYCEHCLQGWETLCEKQQNTGYSVNGG 123
           GHE  G V+A+GSGV+  KEGD VGV WL+ AC  CE+C  GWETLCE Q NTGYS NGG
Sbjct: 68  GHEAAGIVAALGSGVTEFKEGDAVGVAWLHDACLRCEYCETGWETLCEHQHNTGYSCNGG 127

Query: 124 YGEYVVADPNYVGLLPDKVGFVEIAPILCAGVTVYKGLKVTDTRPGQWVVISGIGGLGHV 183
           + EYV+A   +   LP  V F EIAPILCAGVT YKGLK T+ RPG+WV ISG+GGLGHV
Sbjct: 128 FAEYVIASAAFAARLPQNVNFSEIAPILCAGVTTYKGLKETEARPGEWVAISGVGGLGHV 187

Query: 184 AVQYARAMGLRVAAVDIDDAKLNLARRLGAEVAVNARDTDPAAWLQK-EIGGAHGVLVTA 242
           A+QYA+AMGL+V A+D+  AKL+LAR++GA++A+N    D    + K   GGAHGVLVTA
Sbjct: 188 AIQYAKAMGLKVVALDVAAAKLDLARQVGADLALNVLSEDTIEKVLKVTSGGAHGVLVTA 247

Query: 243 VSPKAFSQAIGMVRRGGTIALNGLPPGDFGTPIFDVVLKGITIRGSIVGTRSDLQESLDF 302
           VSP AFSQA+ MVRR GT++L GLPPG+F  PIFDVVLK IT+RGSIVGTR DL E+L F
Sbjct: 248 VSPPAFSQALSMVRRKGTVSLVGLPPGNFPMPIFDVVLKRITVRGSIVGTRRDLDEALAF 307

Query: 303 AAHGDVKATVSTAKLDDVNDVFGRLREGKVEGRVVLDFS 341
           A  G V+A ++ A LDD+ND+F  L+ G +EGR+VLD +
Sbjct: 308 ATEGRVRAEIAKAPLDDINDIFAGLKAGTIEGRMVLDIA 346


Lambda     K      H
   0.319    0.139    0.427 

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: 405
Number of extensions: 16
Number of successful extensions: 2
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: 342
Length of database: 360
Length adjustment: 29
Effective length of query: 313
Effective length of database: 331
Effective search space:   103603
Effective search space used:   103603
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 (21.7 bits)
S2: 49 (23.5 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