GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Ruegeria conchae TW15

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_010442691.1 G7G_RS0117200 ABC transporter ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>NCBI__GCF_000192475.1:WP_010442691.1
          Length = 362

 Score =  293 bits (749), Expect = 7e-84
 Identities = 164/366 (44%), Positives = 218/366 (59%), Gaps = 17/366 (4%)

Query: 4   IQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDIYIG 63
           +++ DL   FG+   + +L++DI + EFLVL+G SGCGKST L  +AGL   T G I+I 
Sbjct: 8   VEVRDLDLHFGEVKVLQELNIDIHEGEFLVLLGSSGCGKSTLLNCIAGLLDVTDGQIFIK 67

Query: 64  GDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDE---RVVEVAE 120
           G ++ ++ P +R I MVFQ YALYP MTV  N+ FGL+         RDE   RV   AE
Sbjct: 68  GQNVTWKEPSDRGIGMVFQSYALYPQMTVEGNLSFGLKNAR----VARDEIAKRVARAAE 123

Query: 121 TLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNL 180
            L I  LL RKP  LSGGQ+QRVA+GRA+VRD +VFL DEPLSNLDAKLR ++R EL+ L
Sbjct: 124 ILQIEPLLKRKPGALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRTDLRVELKRL 183

Query: 181 QDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMI 240
             QL  T +YVTH+Q EAMT+ADRIA+M  G++ Q+ SP E Y+ P N++VA FIG P +
Sbjct: 184 HQQLKNTMIYVTHDQVEAMTLADRIAIMKGGKIMQLGSPDEIYNRPQNIYVAGFIGSPAM 243

Query: 241 NLVRGTRSESTFVGEHFSYPLDEDVMESVDDR-DDFVLGVRPEDIEVADAAPDDAALDDH 299
           N++ G      F G   S PLD    E  D       +G+RPE +   DA    AA    
Sbjct: 244 NMIEGRIDNGHFAGHDLSLPLDGYEFERTDHHAGPVAIGIRPEHVLTGDAVETAAA---- 299

Query: 300 DLQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDRVTVTIPPDKIHLF 359
             +++V +VE  G   ++H            L+   +G+  VT GDR+ +     +  LF
Sbjct: 300 QAEVEVQIVEKLGSDTLVH-----STLGSLNLRFRMDGLSRVTEGDRLRIGFDTSRASLF 354

Query: 360 DAETGT 365
           DA T T
Sbjct: 355 DAVTET 360


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: 341
Number of extensions: 9
Number of successful extensions: 4
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: 362
Length adjustment: 30
Effective length of query: 353
Effective length of database: 332
Effective search space:   117196
Effective search space used:   117196
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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