GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Sinorhizobium meliloti 1021

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate SM_b20419 SM_b20419 glycerol-3-phosphate ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Smeli:SM_b20419
          Length = 349

 Score =  326 bits (835), Expect = 7e-94
 Identities = 183/362 (50%), Positives = 233/362 (64%), Gaps = 22/362 (6%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA +TL DV K Y     GDI A+  +SL I DGEF+VLVGPSGCGKST LRM+AGLE++
Sbjct: 1   MATITLKDVHKTYH----GDIAAIRGVSLAIADGEFIVLVGPSGCGKSTLLRMIAGLESI 56

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           T GE+ + DRV+NG+   +RDIAMVFQ+YALYPH +VR N+S+GL+ +   P +EI +R+
Sbjct: 57  TSGEISIGDRVVNGLEPSERDIAMVFQNYALYPHMTVRQNLSYGLK-NRNTPKEEIERRI 115

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            +    L I   LDRKP QLSGGQ+QRVA+GRAIVR+P  FL DEPLSNLDAKLR +MR 
Sbjct: 116 AKAAKSLEIEPFLDRKPRQLSGGQRQRVAMGRAIVREPAAFLFDEPLSNLDAKLRVQMRV 175

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E++RLQ  LG T+VYVTHDQ EAMT+ DR+ VL+ G ++QVGTP++ Y  P   FVA FI
Sbjct: 176 EIKRLQRALGTTSVYVTHDQLEAMTLADRLVVLNGGRIEQVGTPIELYENPATAFVATFI 235

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASGL-TLGIRPEDVTVGERRSGQR 299
           G PSMNL D +     +                L G  GL T+GIRPED+T+     G  
Sbjct: 236 GSPSMNLLDLNTGNAAWSAPA-----------ALVGKPGLATIGIRPEDITLAGDTDGGE 284

Query: 300 TFDAEVVV--VEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHL 357
            F A V V  VE  G E+ VH    +G+          G+SR+   +   V+    ++H 
Sbjct: 285 RFRARVRVGAVELVGAESYVHGTLANGE---PLVFRVAGRSRMMIDEEVEVAAVAGSLHW 341

Query: 358 FD 359
           FD
Sbjct: 342 FD 343


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: 418
Number of extensions: 27
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: 349
Length adjustment: 30
Effective length of query: 353
Effective length of database: 319
Effective search space:   112607
Effective search space used:   112607
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