GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Flavobacterium beibuense F44-8

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate WP_035136286.1 Q763_RS17105 acyl-CoA dehydrogenase

Query= CharProtDB::CH_091785
         (379 letters)



>NCBI__GCF_000769915.1:WP_035136286.1
          Length = 380

 Score =  393 bits (1009), Expect = e-114
 Identities = 202/374 (54%), Positives = 266/374 (71%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           MDF LT E  ++++  R+FA+NE+ P   E DE + FP E +KKMG+ G +G+    +YG
Sbjct: 1   MDFKLTEEHLMIQKAARDFAQNELLPGVIERDEKQIFPTEQIKKMGELGFLGMMVDPKYG 60

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           G+G D +SY+IA+EE+SKV  +  V++S + SL    +   GTEEQKQKYL  LA GE I
Sbjct: 61  GSGLDAVSYVIAMEEISKVDASASVVMSVNNSLVCWGLETFGTEEQKQKYLTRLATGEII 120

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           GA+ L+EP AG+D+ +Q+T A+ +GDHY++NG+K +ITNG  AD +++ A TD  K  +G
Sbjct: 121 GAFCLSEPEAGSDATSQKTTAIDKGDHYLLNGTKNWITNGSTADVYLVIAQTDIEKKHRG 180

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           I+A I+EKG  GF IG  EQKLGIR S T  L+F D+ VP EN IG++G GF  AMKTL 
Sbjct: 181 INALIVEKGMPGFEIGAKEQKLGIRGSDTHSLMFTDVKVPKENRIGEDGFGFKFAMKTLS 240

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLVY 300
           GGRIGIA+QALGIA GA+  A  Y +ERK FG  +   Q +A+ +ADM V IE+AR+L  
Sbjct: 241 GGRIGIASQALGIASGAYELALKYSQERKAFGTEIFNHQAIAFKLADMAVQIEAARHLCM 300

Query: 301 KAAYLKQAGLPYTVDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAKITE 360
           KAA+ K     Y V  A AKL+A+ VAMD T +AVQ+ GG GY K+Y VER+MRDAKIT+
Sbjct: 301 KAAWDKDNHNNYDVSGAMAKLYASQVAMDTTIEAVQIHGGNGYVKEYHVERLMRDAKITQ 360

Query: 361 IYEGTSEVQKLVIS 374
           IYEGTSE+QK+VIS
Sbjct: 361 IYEGTSEIQKIVIS 374


Lambda     K      H
   0.317    0.135    0.377 

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: 424
Number of extensions: 17
Number of successful extensions: 1
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: 379
Length of database: 380
Length adjustment: 30
Effective length of query: 349
Effective length of database: 350
Effective search space:   122150
Effective search space used:   122150
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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