GapMind for catabolism of small carbon sources

 

Alignments for a candidate for amaA in Pseudomonas fluorescens FW300-N1B4

Align pipecolate oxidase (EC 1.5.3.7) (characterized)
to candidate Pf1N1B4_4356 Gamma-glutamyl-putrescine oxidase (EC1.4.3.-)

Query= metacyc::G1G01-5614-MONOMER
         (432 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4356
          Length = 432

 Score =  139 bits (349), Expect = 2e-37
 Identities = 116/379 (30%), Positives = 176/379 (46%), Gaps = 13/379 (3%)

Query: 34  DVCVIGGGITGLSAAIHLLEQGKSVIVLEAWKIGHGGSGRNVG-LVNAGTWIRPDDV-EA 91
           DVCVIG G TGLS+A+ L E G SV VLEA K+G G SGRN G LVN  ++ R  DV E 
Sbjct: 35  DVCVIGAGYTGLSSALFLSEAGYSVTVLEAAKVGFGASGRNGGQLVN--SYSRDVDVIEE 92

Query: 92  TLGQKQGSRLNKVLGEAPAEVFAMIERLGIDCQAQHKGTLHMAHNATGIADLEARHEQWR 151
             G K    L  ++ E    + + I+   I C     G +  A N   +  L  +   W 
Sbjct: 93  RYGDKTAEVLGSMIFEGADIIRSRIKEYDIQCD-YRPGGIFAALNKKQLNGLAEQKSSWE 151

Query: 152 RRG-ADVELLTGAQCQEYCGTDKISAALLDRRAGTINPMGYTQGLAAAVTRLGGKIFQQS 210
           R G  ++ +L  A  +   G D     LLD + G I+P+    G AAA+ RLGGKI++QS
Sbjct: 152 RYGNKNLRMLDAADIKREVGCDNYVGGLLDMQGGHIHPLNLALGEAAAIIRLGGKIYEQS 211

Query: 211 SVEGLEREGDGWRVKTARGAVRAEKVVISTGAYTEGDWSN-LQKQFFRGYYYQVASKPLQ 269
           +   +   G+   V+TA+G VRA+ ++I+  AY   D  N + ++        V ++PL 
Sbjct: 212 AAVEI-TYGEPITVRTAKGVVRAKYLLIAGNAYLPQDLDNRVTRKSMPCGSQIVVTEPLS 270

Query: 270 GIAADKVLPHGQGSWDTRTVLSSIRRDDQGRLLLGSLGRVDNKPAWFVRSWADRIQSHYY 329
              A  ++ +     D   +L   R     RLL G       +    +           +
Sbjct: 271 EKVARSLIANNYCVEDCNYLLDYYRLTADNRLLYGGGVVYGAREPDDIEQLIRPKILKTF 330

Query: 330 PELGKVEWEMHWTGCIDFTPDHLMRLFEPAPGLVAVTGYNGRGNTTGTVIGRAFAEFLLK 389
           P+L  V+ +  WTG    T   + +          + GY+G G T   + G+  +E +++
Sbjct: 331 PQLKDVKIDYRWTGNFLLTMSRMPQFGRIEKNAYYMQGYSGHGVTCSHLAGKLISE-MIR 389

Query: 390 GEADSL----PIPFSPMSG 404
           G+A+       +P  PM G
Sbjct: 390 GDAERFDAFASLPHMPMLG 408


Lambda     K      H
   0.319    0.135    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: 424
Number of extensions: 21
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: 432
Length of database: 432
Length adjustment: 32
Effective length of query: 400
Effective length of database: 400
Effective search space:   160000
Effective search space used:   160000
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 (21.7 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