GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Maridesulfovibrio zosterae DSM 11974

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_027720856.1 H589_RS0104095 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_000425265.1:WP_027720856.1
          Length = 358

 Score =  199 bits (505), Expect = 1e-55
 Identities = 116/310 (37%), Positives = 172/310 (55%), Gaps = 19/310 (6%)

Query: 23  AVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNG---VSAQD 79
           AV+ ++  +++GE   L+GPSGCGK+T LR +AG E +  G + + D+++ G   V  + 
Sbjct: 19  AVKNVTFSLEEGEIGCLLGPSGCGKTTLLRTIAGFEDIAAGSIIIADKLVAGQRTVPPEK 78

Query: 80  RDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKPGQ 139
           R+I MVFQ YAL+PH  V  N++FG+EE   LP  E  +R+++    + +    D+ P +
Sbjct: 79  RNIGMVFQDYALFPHLKVGENIAFGIEE---LPPAERSKRIDDLLRTVELDGSGDKYPHE 135

Query: 140 LSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYVTHD 199
           LSGGQQQRVAL RA+  +P++ LMDEP SNLD  LR  + TE++ +  +  +T + VTH+
Sbjct: 136 LSGGQQQRVALARALAPEPKLLLMDEPFSNLDVALRETLSTEIREILKDRSITALMVTHN 195

Query: 200 QTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSLSGDTFRG 259
           Q EA  M D+V VL  G +QQ  TP   YH P+N  VAGF+GE         +  +   G
Sbjct: 196 QNEAFAMADKVGVLSCGSMQQWDTPHSIYHHPSNPVVAGFVGEGVF------IDAEIVEG 249

Query: 260 DGFDYPLSGATRD---QLGGASGLTLGIRPEDVTVGERRSGQRTFDAEVVVVEPQGNENA 316
           +     L     D    L   +   L IRPEDV           + AE++    +G    
Sbjct: 250 NTIKCALGELQSDFKLNLESGTQAKLLIRPEDVI----HDDDSPYGAEIIAKTFRGPNIL 305

Query: 317 VHLRFVDGDE 326
             L+  +G+E
Sbjct: 306 YKLKLDNGEE 315


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: 400
Number of extensions: 23
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: 358
Length adjustment: 30
Effective length of query: 353
Effective length of database: 328
Effective search space:   115784
Effective search space used:   115784
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 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