GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Dyella japonica UNC79MFTsu3.2

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

Query= reanno::Smeli:SM_b21106
         (365 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  318 bits (816), Expect = 1e-91
 Identities = 187/365 (51%), Positives = 235/365 (64%), Gaps = 15/365 (4%)

Query: 1   MAPVTLKKLVKRYGALEV-VHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGA 59
           MA V L KL K Y    V V     E+ D E + LVGPSGCGK+T LRMIAGLE +SGG 
Sbjct: 1   MAKVRLDKLRKVYPNGHVGVAEASFEIADGELLVLVGPSGCGKTTLLRMIAGLESISGGT 60

Query: 60  IEIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAA 119
           + IG R VND+ P+ R+I+MVFQ+YALYPHMTVAEN+GF LK+ G+P  EI+ RVAEAA 
Sbjct: 61  LSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLKLRGQPKAEIERRVAEAAR 120

Query: 120 ILDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKL 179
           +L+L   L+ RP+ LSGGQRQRVA+GRA+VR P VFL DEPLSNLDAKLR  +R EI ++
Sbjct: 121 MLELEQRLDSRPAALSGGQRQRVALGRALVRDPKVFLLDEPLSNLDAKLRLSMRVEIARI 180

Query: 180 HARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPM 239
           H R++ATM+YVTHDQ+EAMTL  RIV++  G I+Q+ TP +++  PA  FVAGF+GSP M
Sbjct: 181 HQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFLGSPAM 240

Query: 240 NMEEAVL-TDG--KLAFASGATL--PLPPRFRSLVREGQKVTFGLRPDDVYPSGHGLHAG 294
           N+   +L  DG  KLA   G  +   LP          + +  GLRP+D+      L A 
Sbjct: 241 NLLRGILYRDGGWKLAMPQGELVLGELPQGAALEAWRDRDIVVGLRPEDLL-----LCAD 295

Query: 295 DADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRMLNPRPL-RPGEAVPMSFDLARAH 353
            A A    +L V   EP+GNE  +  +      VSRM  PR L  PG  +   F   R H
Sbjct: 296 AAGAALAAQLEV--VEPVGNEVFLNLRHGELALVSRM-PPRELPAPGSTLHFGFAPERLH 352

Query: 354 LFDGE 358
            FD +
Sbjct: 353 FFDAK 357


Lambda     K      H
   0.320    0.137    0.397 

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: 394
Number of extensions: 16
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: 365
Length of database: 364
Length adjustment: 29
Effective length of query: 336
Effective length of database: 335
Effective search space:   112560
Effective search space used:   112560
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: 49 (23.5 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