GapMind for catabolism of small carbon sources

 

Aligments for a candidate for ans in Pseudomonas fluorescens FW300-N2E2

Align glutaminase (EC 3.5.1.2) (characterized)
to candidate Pf6N2E2_2102 Glutaminase (EC 3.5.1.2)

Query= BRENDA::P0A6W0
         (308 letters)



>lcl|FitnessBrowser__pseudo6_N2E2:Pf6N2E2_2102 Glutaminase (EC
           3.5.1.2)
          Length = 302

 Score =  365 bits (936), Expect = e-106
 Identities = 183/301 (60%), Positives = 232/301 (77%), Gaps = 1/301 (0%)

Query: 8   AILENILRQVRPLIGQGKVADYIPALATVDGSRLGIAICTVDGQLFQAGDAQERFSIQSI 67
           A+L  IL  VRPLIGQGKVADYIPAL TV  ++LGIA+   DG+L+ AGDA+  FS+QSI
Sbjct: 3   ALLNEILDAVRPLIGQGKVADYIPALGTVAPNQLGIAVYGNDGELYCAGDAETAFSVQSI 62

Query: 68  SKVLSLVVAMRHYSEEEIWQRVGKDPSGSPFNSLVQLEMEQGIPRNPFINAGALVVCDML 127
           SKV SLV A+ H S E IW+R+G +PSG PFNSLVQLE E+G PRNPFINAGALV+CD+ 
Sbjct: 63  SKVFSLVQAIGH-SGEAIWERLGHEPSGQPFNSLVQLEFERGRPRNPFINAGALVICDIN 121

Query: 128 QGRLSAPRQRMLEVVRGLSGVSDISYDTVVARSEFEHSARNAAIAWLMKSFGNFHHDVTT 187
           Q R +AP   M + VR LSG   +  D  VA SE++H ARNAA+A+LM+SFGNFH+DV  
Sbjct: 122 QSRFAAPALSMRDFVRRLSGNPQVMVDGKVAESEYQHRARNAAMAYLMQSFGNFHNDVEA 181

Query: 188 VLQNYFHYCALKMSCVELARTFVFLANQGKAIHIDEPVVTPMQARQINALMATSGMYQNA 247
           VL++YF +CAL+MSC++LAR F FLAN G   H  E +++  Q +Q+N++MATSG+Y  A
Sbjct: 182 VLRSYFSHCALRMSCIDLARAFCFLANDGFCKHSGEQILSARQTQQVNSIMATSGLYDEA 241

Query: 248 GEFAWRVGLPAKSGVGGGIVAIVPHEMAIAVWSPELDDAGNSLAGIAVLEQLTKQLGRSV 307
           G FA+RVGLP KSGVGGGIVA+VP    + VWSPEL+ AGNSLAG+A LE +++++G SV
Sbjct: 242 GNFAYRVGLPGKSGVGGGIVAVVPGRFTVCVWSPELNAAGNSLAGMAALELMSQRIGWSV 301

Query: 308 Y 308
           +
Sbjct: 302 F 302


Lambda     K      H
   0.321    0.135    0.395 

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: 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: 308
Length of database: 302
Length adjustment: 27
Effective length of query: 281
Effective length of database: 275
Effective search space:    77275
Effective search space used:    77275
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: 48 (23.1 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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