GapMind for catabolism of small carbon sources

 

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

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

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__Dino:3607124
          Length = 338

 Score =  289 bits (740), Expect = 7e-83
 Identities = 174/367 (47%), Positives = 229/367 (62%), Gaps = 29/367 (7%)

Query: 1   MGQIQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDI 60
           M  I++  + K +G T A+ D++LDI+D EF+V VGPSGCGKST LR LAGLE  +SG I
Sbjct: 1   MAGIKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRI 60

Query: 61  YIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAE 120
            IGG  +    P +RD+AMVFQ YALYPHMTVR+N+ FG++   G+    R ER+ E A 
Sbjct: 61  EIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVN-GFEPDLRKERIAEAAR 119

Query: 121 TLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNL 180
            L + D LDRKP +LSGGQ+QRVA+GRAIV++P VFL DEPLSNLDAKLR +MR EL+ L
Sbjct: 120 VLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGL 179

Query: 181 QDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMI 240
             QL  T +YVTH+Q EAMTMAD+I V++ G ++QV SP + YH+PN+ FVAEFIG P +
Sbjct: 180 HKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAM 239

Query: 241 NLVRGTRSESTFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEVADAAPDDAALDDHD 300
           N+       S+ VG        +D+  S+D    FV G RPE IE+    PD     D  
Sbjct: 240 NVF------SSDVGL-------QDI--SLDASAAFV-GCRPEHIEI---VPD----GDGH 276

Query: 301 LQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDRVTVTIPPDKIHLFD 360
           +   V V E  G +++L+L           + A   G      G  V++     ++H FD
Sbjct: 277 IAATVHVKERLGGESLLYLG----LKGGGQIVARVGGDDETKVGAAVSLRFSRHRLHQFD 332

Query: 361 AETGTAV 367
            E G A+
Sbjct: 333 -EAGRAI 338


Lambda     K      H
   0.317    0.135    0.386 

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: 360
Number of extensions: 17
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: 41 (21.6 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