GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Skermanella stibiiresistens SB22

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_037454711.1 N825_RS16865 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_000576635.1:WP_037454711.1
          Length = 362

 Score =  301 bits (772), Expect = 1e-86
 Identities = 179/380 (47%), Positives = 234/380 (61%), Gaps = 32/380 (8%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA + +  V K Y     G    +  I ++I+D EF+VLVGPSGCGKST LRM+AGLE +
Sbjct: 1   MASVGIAQVRKAY-----GQHEVIHGIDIEIEDEEFVVLVGPSGCGKSTLLRMVAGLEQI 55

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           T GE+ +   V+N V  ++RDIAMVFQ+YALYPH +V  NM+F L+     PD  +++RV
Sbjct: 56  TGGEIAIGGTVVNLVPPKERDIAMVFQNYALYPHMTVFNNMAFSLQLRKSDPD-MVQKRV 114

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            E  D+LG+   LDR P QLSGGQ+QRVA+GRAIVRDP+VFL DEPLSNLDAKLR +MRT
Sbjct: 115 REAADILGLVPYLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRT 174

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E++ L   L  T++YVTHDQ EAMTM DR+ V+ DG ++Q+GTPL+ Y  P N FVAGFI
Sbjct: 175 EIKALHQRLRTTSIYVTHDQVEAMTMADRIVVMHDGHVEQIGTPLELYDYPANTFVAGFI 234

Query: 241 GEPSMNLFDGSLSGDTFRGDG----------FDYPLSGATRDQLGGASGLTLGIRPEDVT 290
           G PSMN F+G     TFR DG            +P+   TR   G    +T GIRP  +T
Sbjct: 235 GSPSMNFFNG-----TFRRDGRAAWVEVAGDIRFPVEPLTRANDG--QSVTYGIRPGHLT 287

Query: 291 V--GERRSG-QRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTT 347
           +  G+   G  +   A + V+EP G++  V  R  + +    F      +     GD T 
Sbjct: 288 LVNGDAAPGFPKGVAATIQVIEPTGDDTVVFCRMANQEACAMFVE----RHAFRPGD-TI 342

Query: 348 VSFPEDAI-HLFDGETGDAL 366
           +  P  A  H+FD  +G  L
Sbjct: 343 MLMPRMANGHVFDSASGHRL 362


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: 424
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: 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: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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