GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gnl in Burkholderia phytofirmans PsJN

Align gluconolactonase (EC 3.1.1.17) (characterized)
to candidate BPHYT_RS24170 BPHYT_RS24170 gluconolactonase

Query= BRENDA::Q64374
         (299 letters)



>FitnessBrowser__BFirm:BPHYT_RS24170
          Length = 309

 Score =  133 bits (334), Expect = 6e-36
 Identities = 97/308 (31%), Positives = 150/308 (48%), Gaps = 24/308 (7%)

Query: 5   KVECVLRENYRCGESPVWEEASQSLLFVDIPSKIICRWDTVSNQVQRVAVDAPVSSVALR 64
           +VE   +     GESPVW  A Q+L +VDIP++ I R    S +     +   V+ +A  
Sbjct: 11  RVEAAGQAPAAVGESPVWRAAEQALYWVDIPAQKIVRLRIDSGERSEWLLPEKVACIAFD 70

Query: 65  QLGGYVATIGTKFCALNW-----ENQSVFV----LAMVDEDKKNNRFNDGKVDPAGRYFA 115
             G  +A   T   AL         ++V V    LA  D    + RFNDG+ D  GR++A
Sbjct: 71  HRGTVLAGCETGLFALTLTESAANGEAVQVTGRKLAAPDFACDDMRFNDGRCDRQGRFWA 130

Query: 116 GTMAEETAPAVLERHQGSLYSLFPDHSVKK--YFDQVDISNGLDWSLDHKIFYYIDS--L 171
           GTM ++ A A   +  G+LY  F +  +      +++   NGL WS D    Y  DS  L
Sbjct: 131 GTMVQDMAAA---KPAGALYR-FDERGMLSAPVVEELITQNGLAWSPDGATMYLSDSHPL 186

Query: 172 SYTVDAFDYDLQTGQISNRRIVYKMEKDEQIPDGMCIDAEGKLWVACYNGGRVIRLDPET 231
              + AFDYD+++G+  NRR+   + +    PDG  +DA+G  W+   + G ++R  PE 
Sbjct: 187 RRQIWAFDYDIESGEPRNRRVFADLNQHAGRPDGAAVDADGCYWICANDAGLLLRFTPE- 245

Query: 232 GKRLQTVKLPVDKTTSCCFGGKDYSEMYVTCARDGLNAEGLLRQPDAGNIFKITGLGVKG 291
           GK  + + +P  K   C FGG++   ++VT  R   NA         G++F +   G+ G
Sbjct: 246 GKLDRQIAVPAIKPAMCAFGGRELDTLFVTSIRPAANA-----SEHDGHLFAVRP-GITG 299

Query: 292 IAPYSYAG 299
           +    +AG
Sbjct: 300 LPEPEFAG 307


Lambda     K      H
   0.319    0.137    0.419 

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: 270
Number of extensions: 17
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: 299
Length of database: 309
Length adjustment: 27
Effective length of query: 272
Effective length of database: 282
Effective search space:    76704
Effective search space used:    76704
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: 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 paper from 2022 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