GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kbl in Sphingomonas koreensis DSMZ 15582

Align 2-amino-3-ketobutyrate coenzyme A ligase (EC 2.3.1.29) (characterized)
to candidate Ga0059261_3672 Ga0059261_3672 7-keto-8-aminopelargonate synthetase and related enzymes

Query= reanno::ANA3:7026975
         (397 letters)



>FitnessBrowser__Korea:Ga0059261_3672
          Length = 369

 Score =  148 bits (373), Expect = 3e-40
 Identities = 106/345 (30%), Positives = 172/345 (49%), Gaps = 8/345 (2%)

Query: 45  VNFCANNYLGLANHPELIKAAQQGLDSH-GFGMASVRFICGTQDIHKQLEASLSEFLGME 103
           ++F +N+YLGLAN   L  A    LD     G    R + G       LEA  +     E
Sbjct: 28  IDFASNDYLGLANDQRLRDAVAAALDRGLAVGSGGSRLLRGNDPEIATLEAEAAAMFRAE 87

Query: 104 DTILYSSCFDANAGLFETLLDAEDAIISDALNHASIIDGVRLCKAKRFRYANNDMADLET 163
             + +S+ F AN  L  TL    D I+ DAL HAS+ DG++L +A     A+ND   ++ 
Sbjct: 88  AALFFSTGFAANVALLATLPQPGDLIVHDALIHASVHDGLKLSRAPSVAAAHNDAQAVDD 147

Query: 164 QLIAAKA-AGARNILIATDGVFSMDGVIANLQGVCDLADKYGALVMVDDSHAVGFVGLNG 222
            + + +   GA    IA + ++SMDG  A +  + ++A ++ A++++D++HA G  G  G
Sbjct: 148 AIASWRGQGGAGTPWIAVESLYSMDGDRAPIAALAEVAARHDAMLIIDEAHATGIWGNGG 207

Query: 223 RGSHEHCGVMGRVDIIT-GTLGKALGGASGGFTSGKKEVIDWLRQRSRPYLFSNSLAPSI 281
           RG      + G+ +IIT  T GKAL G  G    G +  ID+L  R+RP++FS + +P +
Sbjct: 208 RGL--AATLEGQPNIITLHTCGKAL-GCEGALVCGARVFIDFLVNRARPFIFSTAPSPLM 264

Query: 282 VTASIHVLEMLKSGQALREAVWENSRYFREKMSAAGFTLGGADHAIIPVMIGDAKLASDF 341
             A    L ++    A RE +     +    ++  G T  G+   ++P+++G        
Sbjct: 265 AAAVREALRIVADEPARRETLHWLIAHAERVLAPLGVTPTGSQ--VLPLIVGGDAETMAR 322

Query: 342 ANRLLAEHIYVIGFSFPVVPKGQARIRTQMSAAHTREQLDKAIEA 386
           A  L A+   V G   P VP G AR+R  ++   T+  +D+  +A
Sbjct: 323 AAALQAKGFDVRGIRPPTVPAGTARLRISLTLNVTQGDIDRLADA 367


Lambda     K      H
   0.321    0.134    0.385 

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: 314
Number of extensions: 11
Number of successful extensions: 5
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: 397
Length of database: 369
Length adjustment: 30
Effective length of query: 367
Effective length of database: 339
Effective search space:   124413
Effective search space used:   124413
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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