GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Marinicella litoralis KMM 3900

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_099019484.1 CCS90_RS10280 acyl-CoA dehydrogenase

Query= reanno::SB2B:6937192
         (389 letters)



>NCBI__GCF_002591915.1:WP_099019484.1
          Length = 387

 Score =  478 bits (1231), Expect = e-139
 Identities = 235/380 (61%), Positives = 292/380 (76%), Gaps = 2/380 (0%)

Query: 12  LGEDVDMLRDAVYEFAKGEIAPLAEKVDRDNAFPNELWAKFGDMGLLGVTVAEEYGGVNM 71
           L E++++LRD V +F   EIAP AEK+D+DN FP +LW K GD+GLLG+TV  EYGG  M
Sbjct: 7   LSEELELLRDTVRKFTAEEIAPRAEKIDQDNLFPADLWQKMGDLGLLGMTVPGEYGGSEM 66

Query: 72  GYLAHVVAMEEISRASASIGLSYGAHSNLCVNQIYRNGNEAQRAKYLPKLISGEHIGALA 131
           GYLAH++AMEEISR SAS+GLSYGAHSNLCV  +Y++  EAQR +YLPKL SGE++GALA
Sbjct: 67  GYLAHLIAMEEISRGSASVGLSYGAHSNLCVTNLYKHATEAQRQQYLPKLCSGEYVGALA 126

Query: 132 MSEPNAGSDVV-SMKLHARKEGDRYILNGNKMWITNGPDAHTYVIYAKT-DLDKGPHGIT 189
           MSEP AGSDVV SM   A K+G+ +I NGNKMWITNGPDA   ++Y +T D   G   +T
Sbjct: 127 MSEPGAGSDVVGSMSCTAVKDGEYWIANGNKMWITNGPDADVLIVYMRTADQSAGSKCMT 186

Query: 190 AFIVERGFKGFSQAQKLDKLGMRGSNTCELVFEDCEVPEENILGGLNNGVKVLMSGLDYE 249
           AF++E+G  GFS AQKLDKLGMRGSNTCELVFEDC++ E  ILG +N GV +LM GL+ E
Sbjct: 187 AFLIEKGMPGFSTAQKLDKLGMRGSNTCELVFEDCKIHESQILGQVNQGVTILMGGLNTE 246

Query: 250 RVVLSGGPLGIMTACMDIVVPYVHERVQFGKSIGEFQLVQGKLADMYTGMNAAKSYVYNV 309
           R+VLSGGP+GIM A MD  VPY  ER QFGK +G+F L+Q K+  MYT + A++ + Y +
Sbjct: 247 RLVLSGGPIGIMQAAMDAAVPYTAERKQFGKDLGQFGLMQAKIGKMYTDLQASRYFAYGI 306

Query: 310 ARACDRGETTRKDAAGVILYAAELATKMALDAIQLLGGNGYVNEYATGRLLRDAKLYEIG 369
           A+  D G  +R D A  + +A+  A ++AL+AIQ LGGNGY+NEY TGRLLRDAKLY+IG
Sbjct: 307 AKDYDLGIESRLDPAACLYFASSSAVQVALEAIQTLGGNGYINEYPTGRLLRDAKLYDIG 366

Query: 370 AGTSEIRRMLIGRELFNETK 389
           AGT+EIR MLIGREL+   K
Sbjct: 367 AGTNEIRLMLIGRELYRNAK 386


Lambda     K      H
   0.318    0.137    0.396 

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: 501
Number of extensions: 16
Number of successful extensions: 3
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: 389
Length of database: 387
Length adjustment: 30
Effective length of query: 359
Effective length of database: 357
Effective search space:   128163
Effective search space used:   128163
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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