GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Phaeobacter inhibens BS107

Align isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate GFF1551 PGA1_c15710 acyl-CoA dehydrogenase

Query= BRENDA::Q75N94
         (430 letters)



>FitnessBrowser__Phaeo:GFF1551
          Length = 406

 Score =  191 bits (486), Expect = 3e-53
 Identities = 122/348 (35%), Positives = 184/348 (52%), Gaps = 11/348 (3%)

Query: 78  EFPAEMWKKLGDAGFLGITANEDYGGLGMGYQAHCIVMEELSRASGSIALSYAAHSQLCV 137
           E   E+++++G+ G LG T  E YGGLG GY ++ +V  E+ R         +  S L +
Sbjct: 61  ETDPEIFREMGEMGLLGTTIPEQYGGLGAGYVSYGLVAREVERVDSGYRSMMSVQSSLVM 120

Query: 138 NQLSLNGSPEQKERFLPGLLSGDKIGALAMSEHSAGSDVVSMKTTAKEVDGGYVLNGTKM 197
             +   GS EQ++++LP L SG+ IG   ++E  AGSD   MKT A++ DGGY L G+KM
Sbjct: 121 YPIYAYGSEEQRQKYLPKLSSGEWIGCFGLTEPDAGSDPAGMKTRAEKTDGGYRLTGSKM 180

Query: 198 WITNGPDADFIVVYAKTEPQKGSKGITAFVVEKTFDGFSCARKLDKLGMRGSNTGELIFE 257
           WI+N P AD  VV+AK+E   G   I  FV+EK   G S  +  +K  +R S TGE++ +
Sbjct: 181 WISNAPIADVFVVWAKSEAHGGK--IRGFVLEKGMKGLSAPKIANKASLRASITGEIVMD 238

Query: 258 DVFVPKENVLGEVNRGVKVLMEGLDLERLVLSAGPLGIMQAALDLVLPYTHVRKQFGTPI 317
            V V  + +L  V  G+K     L+  R  +S G +G  +A       Y   RKQFG P+
Sbjct: 239 GVEVGDDALLPHV-EGLKGPFGCLNRARYGISWGAMGAAEACWHAARQYGLDRKQFGRPL 297

Query: 318 AHNQLIQGKLADMYTKLQASRAYTYSTARHIDNSASLSE-VSIRTQDCAGAILYAAERAT 376
           A+ QL Q KLA+M T++      +    R +D + +  E +SI  ++  G       +A 
Sbjct: 298 ANTQLFQLKLANMQTEITLGLQASLRVGRLMDEANAAPEMISIVKRNNCG-------KAL 350

Query: 377 ECALDAIQLMGGNGYINELPAGRLLRDAKLYEIGAGTSEIRRMVIGRA 424
           E A  A  + GGNG   E    R + + +      GT ++  +++GRA
Sbjct: 351 EIARHARDMHGGNGISLEFGVIRHMVNLETVNTYEGTHDVHALILGRA 398


Lambda     K      H
   0.317    0.134    0.380 

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: 389
Number of extensions: 24
Number of successful extensions: 4
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: 430
Length of database: 406
Length adjustment: 32
Effective length of query: 398
Effective length of database: 374
Effective search space:   148852
Effective search space used:   148852
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