GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Phaeacidiphilus oryzae TH49

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_037572389.1 BS73_RS14235 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_000744815.1:WP_037572389.1
          Length = 386

 Score =  223 bits (568), Expect = 7e-63
 Identities = 144/367 (39%), Positives = 199/367 (54%), Gaps = 22/367 (5%)

Query: 4   LTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEG 63
           L L  +TK +     G   AV+ + L I  G F  L+G SGCGK+TTLRM++GLE  T G
Sbjct: 19  LRLTGLTKKF-----GSFTAVDGVDLTIAQGSFFALLGASGCGKTTTLRMISGLEAPTAG 73

Query: 64  ELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEET 123
            + L D+ +       R +  VFQ+YAL+PH  +  N++FGL    G+    +++ VE+ 
Sbjct: 74  RIHLGDQDVTDRKPYRRPVNTVFQNYALFPHLDIFENVAFGLRRR-GIRS--VKKPVEDM 130

Query: 124 TDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQ 183
            D++ +  L  RKP QLSGGQQQR+AL RA++  P+V L+DEPL  LD KLR +M+ EL+
Sbjct: 131 LDLVELGHLARRKPTQLSGGQQQRIALARALINQPQVLLLDEPLGALDLKLRRQMQIELK 190

Query: 184 RLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEP 243
           R+Q E+G+T V+VTHDQ EAMTM D +AV++ G ++Q+G+P + Y  PN  FVA F+G+ 
Sbjct: 191 RIQLEVGLTFVHVTHDQEEAMTMADTIAVMNHGRIEQLGSPAELYENPNTTFVANFLGQ- 249

Query: 244 SMNLFDG---SLSGDTFR--GDGFDYPLSGATRDQLGGASGLTLGIRPEDV----TVGER 294
             NL  G   S+SGD  +    G    L  A      G   + LG+RPE V    T  E 
Sbjct: 250 -SNLIAGTVESVSGDVVQVAAHGRSLALPAARCRTTSGP--VILGVRPEKVRIAKTEAEV 306

Query: 295 RSGQRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDA 354
            SG      +V      G      +    G+E   F    TGQ     G    V +    
Sbjct: 307 PSGANHLTGKVTDASFIGVSTQYLVELPSGEELAVF-EQNTGQEIQRPGAEVVVHWDPSQ 365

Query: 355 IHLFDGE 361
               DGE
Sbjct: 366 GFGLDGE 372


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: 441
Number of extensions: 22
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: 386
Length adjustment: 30
Effective length of query: 353
Effective length of database: 356
Effective search space:   125668
Effective search space used:   125668
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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