GapMind for catabolism of small carbon sources

 

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

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  294 bits (753), Expect = 2e-84
 Identities = 171/372 (45%), Positives = 228/372 (61%), Gaps = 26/372 (6%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA++ LD + KVY +      V V E S +I DGE LVLVGPSGCGK+T LRM+AGLE++
Sbjct: 1   MAKVRLDKLRKVYPNGH----VGVAEASFEIADGELLVLVGPSGCGKTTLLRMIAGLESI 56

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           + G L + +RV+N ++ +DRDIAMVFQ+YALYPH +V  N+ FGL+   G P  EI +RV
Sbjct: 57  SGGTLSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLK-LRGQPKAEIERRV 115

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            E   ML +   LD +P  LSGGQ+QRVALGRA+VRDP+VFL+DEPLSNLDAKLR  MR 
Sbjct: 116 AEAARMLELEQRLDSRPAALSGGQRQRVALGRALVRDPKVFLLDEPLSNLDAKLRLSMRV 175

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E+ R+   L  T VYVTHDQ EAMT+G R+ VL+ G +QQ+ TP++ Y  P NLFVAGF+
Sbjct: 176 EIARIHQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFL 235

Query: 241 GEPSMNLFDGSL-----------SGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDV 289
           G P+MNL  G L            G+   G+        A RD+      + +G+RPED+
Sbjct: 236 GSPAMNLLRGILYRDGGWKLAMPQGELVLGELPQGAALEAWRDR-----DIVVGLRPEDL 290

Query: 290 TVGERRSGQRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVS 349
            +    +G     A++ VVEP GNE  ++LR  +        +    +     G      
Sbjct: 291 LLCADAAG-AALAAQLEVVEPVGNEVFLNLRHGE----LALVSRMPPRELPAPGSTLHFG 345

Query: 350 FPEDAIHLFDGE 361
           F  + +H FD +
Sbjct: 346 FAPERLHFFDAK 357


Lambda     K      H
   0.316    0.136    0.384 

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: 413
Number of extensions: 22
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: 383
Length of database: 364
Length adjustment: 30
Effective length of query: 353
Effective length of database: 334
Effective search space:   117902
Effective search space used:   117902
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: 42 (22.0 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