GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Caulobacter crescentus NA1000

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate CCNA_02254 CCNA_02254 isovaleryl-CoA dehydrogenase

Query= CharProtDB::CH_091785
         (379 letters)



>FitnessBrowser__Caulo:CCNA_02254
          Length = 386

 Score =  298 bits (762), Expect = 2e-85
 Identities = 158/377 (41%), Positives = 234/377 (62%), Gaps = 2/377 (0%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           MDF L    + +R+    FA +++ PIAA+IDET  FP E    MG  G+ GI   +E+G
Sbjct: 9   MDFALGETADAIRETTARFAADKIAPIAAKIDETNSFPRELWVPMGDLGLHGITVEEEFG 68

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           G G   L +++A+EE+S+   + G+   AH++LC + I    T EQK +YL  L  GE +
Sbjct: 69  GLGLGYLEHVVAMEEVSRASASVGLSYGAHSNLCVNQIRRWATPEQKARYLPKLISGEHV 128

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           G+  ++E  AG+D  + +  A   GD Y++NG+K +ITN   ADT V++A T   +G++G
Sbjct: 129 GSLAMSEAGAGSDVVSMKLRAEQVGDRYILNGTKFWITNAPHADTLVVYAKTG--EGSRG 186

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           I+AFI+EKG KGFS+ K   K+G+R S T ELVFED  +P EN++G  G G  + M  LD
Sbjct: 187 ITAFIVEKGMKGFSVSKKLDKMGMRGSDTAELVFEDCEIPEENVMGPVGGGVGVLMSGLD 246

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLVY 300
             R  +AA  LGI +   +    Y+++RKQFG+ +  FQ +   +ADM VA+ SAR  VY
Sbjct: 247 YERAVLAAGPLGIMQACLDVVLPYVRDRKQFGQPIGSFQLMQGKIADMYVALNSARAYVY 306

Query: 301 KAAYLKQAGLPYTVDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAKITE 360
             A    AG     DAA A L A+  A+ V+ +A+Q  GG GYTK++PVER++RDAK+ +
Sbjct: 307 AVAKACDAGKTTRFDAAGAILMASENAVKVSLEAIQALGGAGYTKEWPVERLLRDAKLYD 366

Query: 361 IYEGTSEVQKLVISGKI 377
           I  GT+E+++ +I  ++
Sbjct: 367 IGAGTNEIRRFLIGREL 383


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: 378
Number of extensions: 13
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: 379
Length of database: 386
Length adjustment: 30
Effective length of query: 349
Effective length of database: 356
Effective search space:   124244
Effective search space used:   124244
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 17 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