GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Billgrantia desiderata SP1

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_086509502.1 BZY95_RS08430 acyl-CoA dehydrogenase family protein

Query= reanno::Smeli:SM_b21121
         (387 letters)



>NCBI__GCF_002151265.1:WP_086509502.1
          Length = 385

 Score =  279 bits (714), Expect = 8e-80
 Identities = 150/368 (40%), Positives = 221/368 (60%), Gaps = 1/368 (0%)

Query: 20  SVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHGGAGLGYLAHCVAME 79
           ++RRF  + +AP  +  + +   P SLW+++GE GLLGI   EA GG+G  +    +A+E
Sbjct: 15  TIRRFLEQEVAPHYEAWEEAGEMPRSLWQQLGEAGLLGIDLPEALGGSGADFAIVQLALE 74

Query: 80  EISRAS-ASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHVGALAMSEPGAGSD 138
           EISR     +  +Y  H+N+ +  +   G PAQ+ R+LP + SGE +GA+AM+EPGAGSD
Sbjct: 75  EISRQGFGGLASAYNIHANIVMPYLLHIGTPAQRERWLPAMASGETIGAIAMTEPGAGSD 134

Query: 139 VVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRGITAFLVEKAFPGF 198
           + +MK +A +    + L+GSK++ITNG  AD+++V AKTDPAAG RG++ FLV+    GF
Sbjct: 135 LAAMKTRASRTESGWRLDGSKLFITNGQIADLVIVCAKTDPAAGARGVSLFLVDTTLAGF 194

Query: 199 SAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGLDYERVVLSAGPLGI 258
           S GQ + K+G   S+T+EL F D  +PEE +LG  G G   LM  L  ER+ ++A  LG 
Sbjct: 195 SRGQPIKKIGQHASDTAELFFDDLRLPEEALLGEAGAGFAYLMQELPRERLGVAAQALGA 254

Query: 259 MAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVYAVAAACDRGETAR 318
           M   L + + Y+ ER+ FG+ +GEFQ  +  LA++   ++  RAY     A   +GE   
Sbjct: 255 MEGALALTLDYVRERRAFGRAVGEFQNTRFTLAEVRAQIDMGRAYFEQCVAKYRQGEMNG 314

Query: 319 KDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLYEIGAGTSEIRRMLI 378
            DAA   L  +E         +Q  GG GYT +YP  R   DA++  + AGTSEI + +I
Sbjct: 315 TDAAILKLQLSEMQCRTIDACLQLFGGYGYTREYPISRFYLDARVQTLYAGTSEIMKEVI 374

Query: 379 GRELFAET 386
            R L  ++
Sbjct: 375 ARSLLGKS 382


Lambda     K      H
   0.318    0.135    0.391 

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: 317
Number of extensions: 12
Number of successful extensions: 2
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: 387
Length of database: 385
Length adjustment: 30
Effective length of query: 357
Effective length of database: 355
Effective search space:   126735
Effective search space used:   126735
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 Apr 09 2024. 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