GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fdh in Pseudomonas simiae WCS417

Align L-fucose dehydrogenase (EC 1.1.1.122) (characterized)
to candidate GFF2315 PS417_11805 D-threo-aldose 1-dehydrogenase

Query= reanno::BFirm:BPHYT_RS34225
         (346 letters)



>FitnessBrowser__WCS417:GFF2315
          Length = 334

 Score =  245 bits (626), Expect = 1e-69
 Identities = 146/328 (44%), Positives = 194/328 (59%), Gaps = 13/328 (3%)

Query: 25  LGLGTAPLGGLYRDLSDEEAHATIAAAWDAGVRYFDTAPHYGNTKAEHRLGDALRRYPRA 84
           LG GTAPLG ++R + ++EA AT+ AAW+AGVRYFDTAP YG+  +E RLG AL +Y R 
Sbjct: 11  LGFGTAPLGNMFRAIPEDEAQATVEAAWNAGVRYFDTAPFYGSGLSEIRLGHALSQYNRD 70

Query: 85  DYVLSTKVGRRFVPR----TTPFDDKEG-WQNPLPFEAIYDYTHDGILRSFEDSQQRLGI 139
           D+VLSTKVGR  +           +K G +++  P + + DY+ D  LRS EDS  RL  
Sbjct: 71  DFVLSTKVGRVILDEIEDSARDLGEKSGVFEHGRPNKMLNDYSADATLRSIEDSLTRLNT 130

Query: 140 VDIDILLVHDIGRVTHGDNHPHYWRQLTEGGGFRALDALRSSGAIKAVGLGVN--EGAAI 197
             +DI+ +HDI +  +GD    Y+ Q    G F+ L  LR  G IKA GLGVN  E   +
Sbjct: 131 DRLDIVWIHDIAQDFYGDQWLEYFNQ-ARTGAFKVLTRLREEGVIKAWGLGVNRVEPCEL 189

Query: 198 LDAMAEFDIDCALLAGRYTLLE-QTTLDDLLPACEKRGVSILLGGAFNSGILARGVQGDL 256
              + E   D  LLAGRYTLL+    L  L+ A   + V I++GG ++SGILA G     
Sbjct: 190 TLDLTEAQPDGFLLAGRYTLLDHDRALQRLMDAALAQNVEIVVGGPYSSGILAGGAH--- 246

Query: 257 KFNYGEAPPEVIERVARLEAVCRTHGVPLAAAALQFPYAHPTVATVLTGARSADELRENA 316
            F Y +A P +I +V ++ A+ +  GV + AAALQF  AHP VA V+ GA     + E+ 
Sbjct: 247 -FEYQQASPAIIRKVEQIRAIAQAFGVSVKAAALQFSLAHPAVAAVIPGASRPGRIAEDV 305

Query: 317 ASFELPIPAALWFALREEGLLDSRAPAP 344
           A+    IPAA W ALRE  L+  RAP P
Sbjct: 306 AALSETIPAAFWQALREARLISDRAPLP 333


Lambda     K      H
   0.320    0.139    0.421 

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: 273
Number of extensions: 14
Number of successful extensions: 6
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: 346
Length of database: 334
Length adjustment: 28
Effective length of query: 318
Effective length of database: 306
Effective search space:    97308
Effective search space used:    97308
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 Sep 17 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