GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Sinorhizobium meliloti 1021

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate SM_b20661 SM_b20661 sugar uptake ABC transporter ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__Smeli:SM_b20661
          Length = 355

 Score =  291 bits (744), Expect = 3e-83
 Identities = 170/368 (46%), Positives = 227/368 (61%), Gaps = 22/368 (5%)

Query: 1   MGQIQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDI 60
           M  +   D+ K FG    +  ++++I+D EF++LVGPSGCGKST LRMLAGLE  T+G+I
Sbjct: 1   MAGVDFVDVRKSFGAFPVIKGVNIEIEDGEFVILVGPSGCGKSTLLRMLAGLENITAGEI 60

Query: 61  YIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAE 120
            IG   +N   P++RDIAMVFQ+YALYPHMTV  N+ F L        +E D+RV   AE
Sbjct: 61  RIGNQVVNRLPPKDRDIAMVFQNYALYPHMTVADNMAFSLMLA-ARPKSEIDKRVGVAAE 119

Query: 121 TLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNL 180
            LG++ LLDR P +LSGGQ+QRVA+GRAIVRDP+VFL DEPLSNLDAKLR  MR E++ L
Sbjct: 120 ILGLSKLLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVAMRAEIKEL 179

Query: 181 QDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMI 240
             +L  TTVYVTH+Q EAMTMAD+I VM DG ++Q+ +P E Y  P NLFVA FIG P +
Sbjct: 180 HQRLKTTTVYVTHDQIEAMTMADKIVVMHDGIVEQIGAPLELYDNPANLFVAGFIGSPAM 239

Query: 241 NLVRG---TRSESTFV-GEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEVADAAPDDAAL 296
           N+++G       S F+  +  + P+      +     D V G+RPE +          AL
Sbjct: 240 NMLKGRLDPADPSVFLTADGTALPVARPA--AAAQGRDLVYGLRPEYM----------AL 287

Query: 297 DDHDLQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDRVTVTIPPDKI 356
           D + L  ++ V+EP G +  L      +    D      E ++    G+ + + I    +
Sbjct: 288 DPNGLPAEIAVIEPTGYETQLIA----RLGGHDVTCVFRERVN-AKPGETIHLAIDAAHV 342

Query: 357 HLFDAETG 364
           HLFDA TG
Sbjct: 343 HLFDAGTG 350


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: 340
Number of extensions: 7
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: 355
Length adjustment: 30
Effective length of query: 353
Effective length of database: 325
Effective search space:   114725
Effective search space used:   114725
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