GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Pseudomonas stutzeri RCH2

Align TRAP dicarboxylate transport system, periplasmic component (DctP-like) (characterized, see rationale)
to candidate GFF2613 Psest_2664 tripartite ATP-independent periplasmic transporter solute receptor, DctP family

Query= uniprot:G8AR24
         (337 letters)



>FitnessBrowser__psRCH2:GFF2613
          Length = 329

 Score =  161 bits (408), Expect = 2e-44
 Identities = 101/324 (31%), Positives = 173/324 (53%), Gaps = 11/324 (3%)

Query: 9   LATGLAAAILAPVAASAQDIKPRLIRFGYGLSESSNQGRAVKFFVEDMAKRSGGKLKVKG 68
           LA  L+ +I   V A      P  I+F + +++++ +G+    F +   +R  GK+KV+ 
Sbjct: 9   LACALSFSIAGLVHAD-----PVTIKFAHVVADNTPKGQGALLFKKLAEERLPGKVKVEV 63

Query: 69  FADASLGSDIQMQNALIGGAQEMMVGSTATLVGIVKDFAVFDLPFLFNNEQEADAVFDGP 128
           + ++SL  D +   AL+ G   M+  S A      K   ++DLPFLF++   AD    GP
Sbjct: 64  YPNSSLFGDGKEMEALLLGDVHMLAPSLAKFEHYAKAIQIYDLPFLFDDLAAADRFQSGP 123

Query: 129 FGQKLAAKLNDKGLVGLVYWENGFRNLTNSKRPVEKVEDLKGIKLRVMQNPVYIDMFNGF 188
            G+ L   + DK + GL YW NG + L+ +K P+ + +D +G+K RV  + V  + F   
Sbjct: 124 QGKALLRAMEDKNITGLAYWHNGMKQLSANK-PLREPKDARGLKFRVQASAVLDEQFKAV 182

Query: 189 GANAVPLSFSELFTAMETGTVDGQENPVTTIQSSKFYEVQKYLTISKHVYSPWIVLASKR 248
            AN   +SF+E++  ++TG V+G EN  +  +S K +EVQ Y+T S H    ++V+ + +
Sbjct: 183 RANPRKMSFAEVYQGLQTGVVNGTENTWSNYESQKVHEVQPYMTASDHGLIDYMVITNTK 242

Query: 249 WYDGLSAD---ERKIINEAAVASRDFERKDSREASKQSIAYLKDKGMQINELSDAELGRM 305
           +++GL  D   E + I E   A  + +  D  + ++Q+IA       +I EL+  +  + 
Sbjct: 243 FWNGLPEDLRGELETIMEEVTAEVNRQADDLNQQARQAIA--ASGKTEIIELTPEQRAQW 300

Query: 306 REMVKPAMDKFAADGGADLLNELQ 329
           RE +KP   KF  + GA+L+   Q
Sbjct: 301 REAMKPVWKKFENEIGAELIEAAQ 324


Lambda     K      H
   0.317    0.134    0.372 

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: 222
Number of extensions: 11
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: 337
Length of database: 329
Length adjustment: 28
Effective length of query: 309
Effective length of database: 301
Effective search space:    93009
Effective search space used:    93009
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. 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