GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Ruegeria conchae TW15

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_010442787.1 G7G_RS0117695 isovaleryl-CoA dehydrogenase

Query= reanno::pseudo5_N2C3_1:AO356_26355
         (375 letters)



>NCBI__GCF_000192475.1:WP_010442787.1
          Length = 387

 Score =  288 bits (736), Expect = 2e-82
 Identities = 154/372 (41%), Positives = 225/372 (60%), Gaps = 2/372 (0%)

Query: 5   EEQTQIRDMARQFAQERLKPFAAEWDREHRFPREAIAEMAELGFFGMLVPEQWGGCDTGY 64
           E+   +R+M  ++AQER+KP AAE D  + FP E   EM +LG  G+ VPE++GG    Y
Sbjct: 12  EDVNALREMVHRWAQERVKPMAAEIDASNAFPNELWKEMGDLGLLGVTVPEEYGGAGMSY 71

Query: 65  LAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKF-GNDEQKAKFLTPLASGAMLGAFAL 123
           LA+ + +EE+A    + S     H+++ CV  +K  G DEQK K+L  L SG  +GA A+
Sbjct: 72  LAHTIAVEEVARASASVSLSYGAHSNL-CVNQIKLNGTDEQKQKYLPRLISGDHVGALAM 130

Query: 124 TEPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           +E  AGSD  S+K RA    DHY LNG K +IT+G +A  ++V+A TDP AG +GI+AF+
Sbjct: 131 SESSAGSDVVSMKLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDPEAGSKGITAFL 190

Query: 184 VPTDSPGYSVARVEDKLGQHASDTCQILFEEVKVPVGNRLGEEGEGYKIALANLEGGRVG 243
           +  +  G+S +   DKLG   S+T +++FE+V+VP  N LGEEG G  + ++ L+  RV 
Sbjct: 191 IEKEMKGFSTSPHFDKLGMRGSNTAELIFEDVEVPFENVLGEEGRGVAVLMSGLDYERVV 250

Query: 244 IAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           +A    G+  A  +    Y  ER  FGKPI   Q +  ++ADM T +  AR  V+  A  
Sbjct: 251 LAGIGTGIMAACLDEVMPYLAERKQFGKPIGSFQLMQGKIADMYTAMNSARAYVYEVAKA 310

Query: 304 RDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYEGT 363
            D G     +A+   L+ASE A      A+Q LGG G+L+D P+ RI+RD ++ +I  GT
Sbjct: 311 CDRGDVTRQDAAACCLYASEQAMVQAHQAVQALGGAGFLSDSPVSRIFRDAKLMEIGAGT 370

Query: 364 SDIQRMVISRNL 375
           S+I+RM+I R +
Sbjct: 371 SEIRRMLIGREM 382


Lambda     K      H
   0.320    0.134    0.388 

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: 315
Number of extensions: 14
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: 375
Length of database: 387
Length adjustment: 30
Effective length of query: 345
Effective length of database: 357
Effective search space:   123165
Effective search space used:   123165
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 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