GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kbl in Shewanella loihica PV-4

Align glycine C-acetyltransferase (EC 2.3.1.29) (characterized)
to candidate 5209242 Shew_1720 8-amino-7-oxononanoate synthase (RefSeq)

Query= BRENDA::P0AB77
         (398 letters)



>FitnessBrowser__PV4:5209242
          Length = 382

 Score =  194 bits (494), Expect = 3e-54
 Identities = 127/384 (33%), Positives = 199/384 (51%), Gaps = 12/384 (3%)

Query: 7   QQLTNDLETARAEGLFKEERIIT-SAQQADITVADGSHVINFCANNYLGLANHPDLIAAA 65
           Q++ + ++ A   GL +  +++T S   A+  V  GS   NF +N+YLGL+  P+LI A 
Sbjct: 6   QKIDDKMQRAEQSGLLRRRQLLTQSVGSANRLVHQGSIKHNFASNDYLGLSQSPELIEAL 65

Query: 66  KAGMDSHGFGMASVRFICGTQDSHKELEQKLAAFLGMEDAILYSSCFDANGGLFETLLGA 125
             G   +G G  +   + G  D+H  LEQ L    G E A+L+SS F AN  L +TLL  
Sbjct: 66  GEGARLYGVGSGASPLVTGYSDAHAALEQALCEATGHEAALLFSSGFSANSALMKTLLDK 125

Query: 126 EDAIISDALNHASIIDGVRLCKAKRYRYANNDMQELEARLKEAREAGARHVLIATDGVFS 185
           E  +++D L HAS+IDG+    A+  R+A+ND+   + RL +  +     + + T+ VFS
Sbjct: 126 ESVVVADKLIHASLIDGLLESGAQLKRFAHNDLGAAK-RLVDKHQP----LTVVTESVFS 180

Query: 186 MDGVIANLKGVCDLADKYDALVMVDDSHAVGFVGENGRGSHEYCDVMGRVDIITGTLGKA 245
           MDG +A +  + +L    DA ++VDD+H  G +     G H   D     DI   T GKA
Sbjct: 181 MDGDLAPIDELYELTQANDAWLIVDDAHGFGVL---PLGGHNKVDA-SCCDIQIVTFGKA 236

Query: 246 LGGASGGYTAARKEVVEWLRQRSRPYLFSNSLAPAIVAASIKVLEMVEAGSELRDRLWAN 305
           L G  G         +++L   +R Y++S +L+PA    ++K + +++ G E RDRL   
Sbjct: 237 L-GCQGAAILGSNTCIDFLVAHARDYIYSTALSPASAHVALKAVNLIKNG-ECRDRLAQV 294

Query: 306 ARQFREQMSAAGFTLAGADHAIIPVMLGDAVVAQKFARELQKEGIYVTGFFYPVVPKGQA 365
              F+    A G  L G+   I P+++GD     K  REL+  G +V     P VP+G A
Sbjct: 295 IEAFKLAAKARGLRLLGSHTPIQPLVVGDIDKLAKVNRELKTAGFWVGAIRPPTVPQGSA 354

Query: 366 RIRTQMSAAHTPEQITRAVEAFTR 389
           R+R  ++  HT  ++    +   R
Sbjct: 355 RLRITLNVNHTQAELEALADQLQR 378


Lambda     K      H
   0.320    0.135    0.388 

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: 333
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: 398
Length of database: 382
Length adjustment: 30
Effective length of query: 368
Effective length of database: 352
Effective search space:   129536
Effective search space used:   129536
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: 50 (23.9 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