GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16935 in Halomonas desiderata SP1

Align L-arabinose-binding periplasmic protein; Short=ABP; Flags: Precursor (characterized, see rationale)
to candidate WP_086510988.1 BZY95_RS16550 arabinose ABC transporter substrate-binding protein

Query= uniprot:B2SYR6
         (332 letters)



>NCBI__GCF_002151265.1:WP_086510988.1
          Length = 330

 Score =  340 bits (872), Expect = 3e-98
 Identities = 162/307 (52%), Positives = 223/307 (72%)

Query: 23  AQAADPVKIGFLVKQPEEPWFQDEWKFAEIAAKEKGFTLVKIGAPSGEKVMSAIDNLSAQ 82
           AQA D V+IGF+VKQPE+ WF +E + A    +E GF +V++    G++V+SAIDNL +Q
Sbjct: 24  AQAQDDVRIGFIVKQPEQAWFINEQRAAAERGEELGFRVVRLAGRDGQEVLSAIDNLYSQ 83

Query: 83  KAQGFVICTPDVKLGPGIVAKAKADGLKMMTVDDRLVDGAGKPIASVPHMGISAYNIGKQ 142
            AQGFVIC PDV+LGP ++ +A   G+K++TVDD+ VDG+G+P+  VPH+G+S Y IG+Q
Sbjct: 84  GAQGFVICPPDVRLGPAVMNRANQYGMKVITVDDQFVDGSGEPLEGVPHLGMSGYQIGRQ 143

Query: 143 VGDGLAAEIKKRGWDMKDVGAIDVTYEQLPTAHDRTSGATDALIAAGFPKANIVMAPQAK 202
           VG+ LAAEI+ RGWD + V A+ +T  +LPTA +RT GA+D L+  GFP+ANI  APQ  
Sbjct: 144 VGEALAAEIEARGWDPQQVAALRITNNELPTARERTDGASDVLLEWGFPEANIFDAPQQS 203

Query: 203 TDTENAFNAANIALTKNPQFKHWVAYALNDEGVLGAVRAAEGRGFKADNMIGIGIGGSDS 262
           TDT +AF+AA+  L++  +F+HW+ YALN+E VLG VRA E  G  A ++IG+GI GS +
Sbjct: 204 TDTNSAFSAASPVLSQRSEFEHWIIYALNEESVLGGVRATEQYGLGATDVIGVGINGSGA 263

Query: 263 ALNEFKKPSPTGFYGTVIISPKRHGEETSTLMYDWITQGKAPPPLTLTTGMLATRDNVAD 322
           A  EF + +PTGF+GTV +S  +HG +T+  +Y WIT+   PP  T TTG L TRDN  D
Sbjct: 264 AFAEFSRSNPTGFHGTVAVSSTQHGRQTAENLYRWITEDVEPPANTETTGTLMTRDNWQD 323

Query: 323 VRQKMGL 329
           VR ++GL
Sbjct: 324 VRAELGL 330


Lambda     K      H
   0.316    0.133    0.391 

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: 350
Number of extensions: 17
Number of successful extensions: 1
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: 332
Length of database: 330
Length adjustment: 28
Effective length of query: 304
Effective length of database: 302
Effective search space:    91808
Effective search space used:    91808
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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