GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Alicycliphilus denitrificans K601

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate WP_013518363.1 ALIDE2_RS17025 ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>NCBI__GCF_000204645.1:WP_013518363.1
          Length = 361

 Score =  207 bits (527), Expect = 4e-58
 Identities = 130/358 (36%), Positives = 197/358 (55%), Gaps = 24/358 (6%)

Query: 3   SVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFI 62
           S+  R +SL++G   VL  ++L I+ GEF  LLG SG GKSTLL  IAG      G++ +
Sbjct: 5   SLECRHISLSYGTTPVLRDIDLRIEPGEFFALLGPSGSGKSTLLRLIAGFNQHQSGELLV 64

Query: 63  KDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEILQ 122
             ++++   P  R IGMVFQ+YAL+P MTV  N++FGL   +     + ++V    +++ 
Sbjct: 65  DGQDISGVPPHLRNIGMVFQNYALWPHMTVWDNVAFGLVERRESRDAMRRKVGAVLDLVG 124

Query: 123 IQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLHQS 182
           +    +R+P++LSGGQ+QRVA+ R +V +  + L DEPLSNLD +LR ++R E+K L + 
Sbjct: 125 LAQYARRRPAQLSGGQQQRVALARTIVIEPRLLLLDEPLSNLDKQLRVQMREELKNLQRK 184

Query: 183 LKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMNFF 242
           L  T ++VTHDQ EA+T ADR+AV+  G++QQ+     +Y+ P N FVAGF+G  + N  
Sbjct: 185 LGLTTVFVTHDQEEAMTTADRMAVLDKGILQQVGTAAGLYDYPHNRFVAGFVG--TANLL 242

Query: 243 RGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLG-----LRPEHVKVDEARDGE 297
            GEV      + V A  + F           +P +   +G      RP  V +     GE
Sbjct: 243 EGEV------TAVSADTLTFHARGLGPLALARPAEPPAIGPAALAFRPHQVSMRPR--GE 294

Query: 298 PTHQAVVDIEEPMGADNLL-----WLTFAGQ----SMSVRIAGQRRYPPGSTVRLSFD 346
           P   A V ++  + +   L     +    G+    S     AG+  + PG+ VRL  D
Sbjct: 295 PGDGARVWLDGLVESAEFLGEFSRYRVRVGEVALTSDQPHYAGRGMFAPGAQVRLGLD 352


Lambda     K      H
   0.320    0.137    0.392 

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: 360
Number of extensions: 13
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: 361
Length of database: 361
Length adjustment: 29
Effective length of query: 332
Effective length of database: 332
Effective search space:   110224
Effective search space used:   110224
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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