GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lat in Escherichia coli BW25113

Align lysine ε-aminotransferase (EC 2.6.1.36) (characterized)
to candidate 15866 b1748 succinylornithine transaminase, PLP-dependent (NCBI)

Query= metacyc::MONOMER-12388
         (457 letters)



>FitnessBrowser__Keio:15866
          Length = 406

 Score =  115 bits (289), Expect = 2e-30
 Identities = 95/327 (29%), Positives = 146/327 (44%), Gaps = 29/327 (8%)

Query: 124 RLFFVDGGALAVENALKAALDWKAQKLGLAEPDTDRLQVLHLERSFHGRSGYTMSLTNTE 183
           R+FF + GA A E ALK A  +   + G     + +  ++  + +FHGR+ +T+S     
Sbjct: 98  RVFFCNSGAEANEAALKLARKFAHDRYG-----SHKSGIVAFKNAFHGRTLFTVSAG--- 149

Query: 184 PSKTARFPKFGWPRISSPALQHPPAEHTGANQEAERRALEAAREAFAAADGMIACFIAEP 243
                     G P  S      P         +    A      A A  D      I EP
Sbjct: 150 ----------GQPAYSQDFAPLPA--------DIRHAAYNDINSASALIDDSTCAVIVEP 191

Query: 244 IQGEGGDNHLSAEFLQAMQRLCHENDALFVLDEVQSGCGITGTAWAYQQLGLQPDLVAFG 303
           IQGEGG    S  FLQ ++ LC+ ++AL + DEVQ+G G TG  +AY   G+ PDL+   
Sbjct: 192 IQGEGGVVPASNAFLQGLRELCNRHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLTTA 251

Query: 304 KKTQVCGVMGGGRIDEVPENVFAVSSRISSTWGGNLADMVRATRLLETIERTQVFDTVVQ 363
           K       +G     E    V  V +   +T+GGN      A ++LE I   ++ + V Q
Sbjct: 252 KALGGGFPVGALLATEECARVMTVGTH-GTTYGGNPLASAVAGKVLELINTPEMLNGVKQ 310

Query: 364 RGKYFRDGLEDLAARHPSVVTNARGRGLMCAVDL-PDTRTRNEVLRLMYTEHQVIALPCG 422
           R  +F + L  +  R+  + +  RG GL+    L  D   + + +     +  V+ L  G
Sbjct: 311 RHDWFVERLNTINHRY-GLFSEVRGLGLLIGCVLNADYAGQAKQISQEAAKAGVMVLIAG 369

Query: 423 GRSLRFRPALTIAEHEIDQALQALASS 449
           G  +RF PAL ++E E+   L   A++
Sbjct: 370 GNVVRFAPALNVSEEEVTTGLDRFAAA 396


Lambda     K      H
   0.320    0.135    0.403 

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: 360
Number of extensions: 22
Number of successful extensions: 3
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: 457
Length of database: 406
Length adjustment: 32
Effective length of query: 425
Effective length of database: 374
Effective search space:   158950
Effective search space used:   158950
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: 51 (24.3 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