GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Dinoroseobacter shibae DFL-12

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate 3607124 Dshi_0546 ABC transporter related (RefSeq)

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Dino:3607124
          Length = 338

 Score =  301 bits (771), Expect = 2e-86
 Identities = 171/366 (46%), Positives = 225/366 (61%), Gaps = 28/366 (7%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA + +D + K Y     G   A+ +I+LDI+DGEF+V VGPSGCGKST LR +AGLE V
Sbjct: 1   MAGIKIDKINKFY-----GTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGV 55

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           + G + +  R +  V   DRD+AMVFQSYALYPH +VR NM FG++ + G   D  ++R+
Sbjct: 56  SSGRIEIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVN-GFEPDLRKERI 114

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            E   +L + D LDRKPGQLSGGQ+QRVA+GRAIV++P VFL DEPLSNLDAKLR +MR 
Sbjct: 115 AEAARVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRV 174

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           EL+ L  +LG T +YVTHDQ EAMTM D++ VL+ G ++QVG+P+D YH+PN+ FVA FI
Sbjct: 175 ELEGLHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFI 234

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRT 300
           G P+MN+F              D  L   + D    AS   +G RPE + +     G   
Sbjct: 235 GSPAMNVFSS------------DVGLQDISLD----ASAAFVGCRPEHIEIVP--DGDGH 276

Query: 301 FDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDG 360
             A V V E  G E+ ++L    G    Q  A   G    + G   ++ F    +H FD 
Sbjct: 277 IAATVHVKERLGGESLLYLGLKGGG---QIVARVGGDDETKVGAAVSLRFSRHRLHQFD- 332

Query: 361 ETGDAL 366
           E G A+
Sbjct: 333 EAGRAI 338


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: 420
Number of extensions: 25
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: 383
Length of database: 338
Length adjustment: 29
Effective length of query: 354
Effective length of database: 309
Effective search space:   109386
Effective search space used:   109386
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: 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