GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kbl in Dyella japonica UNC79MFTsu3.2

Align 2-amino-3-ketobutyrate coenzyme A ligase (EC 2.3.1.29) (characterized)
to candidate N515DRAFT_0547 N515DRAFT_0547 8-amino-7-oxononanoate synthase

Query= reanno::Koxy:BWI76_RS27255
         (397 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0547
          Length = 397

 Score =  255 bits (651), Expect = 2e-72
 Identities = 146/368 (39%), Positives = 216/368 (58%), Gaps = 5/368 (1%)

Query: 21  LFKEERIITSAQQADITVGGSQVINFCANNYLGLANHPELIAAAKSGMDSHGFGMASVRF 80
           L +  R I  A+   +  GG +++ FC N+YLGLA HP +IAA K   D  G G  +   
Sbjct: 22  LLRRLRTIEHAEGPWLESGGRRLLGFCGNDYLGLAQHPLVIAAFKRTADDEGVGSTAAHL 81

Query: 81  ICGTQDSHKALEKKLADFLGMEDAILYSSCFDANGGLFETLLGAEDAIISDALNHASIID 140
           ICG +  H ALE+ LAD+ G E A L+S+ + AN G+ + LL A D  + D LNHA ++D
Sbjct: 82  ICGHRAEHAALEEALADWTGRERAALFSTGYLANLGVMQALLRAGDMCVQDKLNHACLLD 141

Query: 141 GVRLCKAKRFRYANNDMVELEARLKEARDAGARHVLIATDGVFSMDGVIANLKGVCDLAD 200
           G  L  A+  RY +ND+     +L    +AGA   L+ATDG+FSMDG +A L+ +  L +
Sbjct: 142 GAALAGAQLKRYPHNDVDGAARQLASRAEAGA---LLATDGIFSMDGDLAPLRELARLCE 198

Query: 201 KYDALVMVDDSHAVGFVGENGRGSHEYCDVMGR-VDIITGTLGKALGGASGGYTAARKEV 259
           + DA +MVDD+H +G +G+NG G+    D+  R V ++  TLGKAL G  G + A    +
Sbjct: 199 QEDATLMVDDAHGLGVLGDNGAGTLSMLDLGQRDVPVLMATLGKAL-GCHGAFVAGSANL 257

Query: 260 VEWLRQRSRPYLFSNSLAPAIVAASIKVLEMVEAGSELRDRLWSNARLFREKMTAAGFIL 319
           VE L Q +R Y+++ ++ PA+ AA++  + +  A S  R++L +  R FR+     G  L
Sbjct: 258 VEGLLQSARTYVYTTAMPPAVAAAALAAVRIARAESWRREKLAALIRRFRDGAQQLGLPL 317

Query: 320 AGADHAIIPVMLGEATVAQEFARELQKEGIYVTGFFYPVVPKGQARIRTQMSAAHTPEQI 379
             +D AI P++LGEAT A   A  L+  G  V     P VP G+AR+R  +SAAH  E +
Sbjct: 318 MPSDTAIQPLLLGEATTAMAAAGALEAVGFLVGAIRPPTVPAGKARLRITLSAAHEEEHV 377

Query: 380 ERAVEAFT 387
           ++ +EA +
Sbjct: 378 DQLLEALS 385


Lambda     K      H
   0.321    0.136    0.390 

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: 409
Number of extensions: 16
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: 397
Length of database: 397
Length adjustment: 31
Effective length of query: 366
Effective length of database: 366
Effective search space:   133956
Effective search space used:   133956
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