GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Sinorhizobium meliloti 1021

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate SMa1400 SMa1400 acyl-CoA dehydrogenase

Query= reanno::Smeli:SM_b21121
         (387 letters)



>FitnessBrowser__Smeli:SMa1400
          Length = 380

 Score =  248 bits (632), Expect = 3e-70
 Identities = 149/366 (40%), Positives = 206/366 (56%), Gaps = 2/366 (0%)

Query: 17  LRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHGGAGLGYLAHCV 76
           +R   R FA E I P+A+  DR   FP  L+ EM +LGL GI   E  GG G   L + V
Sbjct: 10  VRDMARAFADEVIRPMAESLDREERFPAELYGEMAKLGLFGIGVPEHLGGPGFDTLTYAV 69

Query: 77  AMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHVGALAMSEPGAG 136
            MEE+SR  ASV    G    L    + R+G   Q+ R LP +++     A  ++EP AG
Sbjct: 70  VMEELSRGYASVADQCGL-VELISTLLVRHGTEGQQ-RMLPDVLNMSAKVAYCITEPEAG 127

Query: 137 SDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRGITAFLVEKAFP 196
           +DV  ++  A++ GD ++LNG K+WI N P ADV  V A+TD  AG RG++ F+V+    
Sbjct: 128 TDVSGIRTTAERDGDGWMLNGGKIWIHNAPVADVGFVLARTDKEAGNRGMSIFIVDLNSA 187

Query: 197 GFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGLDYERVVLSAGPL 256
           G   G K  K+G R S    L FTD  +P   +LG  G G  ++MS LD  RV ++A  +
Sbjct: 188 GVERGPKEHKMGQRASQVGALTFTDVRLPGGALLGQEGRGFHMMMSVLDKGRVGIAALAV 247

Query: 257 GIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVYAVAAACDRGET 316
           GI  A L+  V Y   RKQFG+ I +FQ +Q  LADM   + AAR  V++ A+  DRG  
Sbjct: 248 GIAQAGLEAAVDYAGTRKQFGKAISDFQGVQWLLADMAKDIEAARLLVHSAASKIDRGLD 307

Query: 317 ARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLYEIGAGTSEIRRM 376
           A K  +    +A + A     +A+Q  GG+GY   +   RL RDAK+ +I  GT++I+RM
Sbjct: 308 ATKACSIAKCFAGDMAVQRTADAVQVFGGSGYIRGFEVERLYRDAKITQIYEGTNQIQRM 367

Query: 377 LIGREL 382
           +I REL
Sbjct: 368 IIAREL 373


Lambda     K      H
   0.318    0.135    0.391 

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: 318
Number of extensions: 20
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: 387
Length of database: 380
Length adjustment: 30
Effective length of query: 357
Effective length of database: 350
Effective search space:   124950
Effective search space used:   124950
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