GapMind for catabolism of small carbon sources

 

Aligments for a candidate for Pf6N2E2_5402 in Sinorhizobium meliloti 1021

Align ABC transporter for D-Alanine, periplasmic substrate-binding component (characterized)
to candidate SMc00676 SMc00676 amino acid-binding periplasmic signal peptide protein

Query= reanno::pseudo6_N2E2:Pf6N2E2_5402
         (343 letters)



>lcl|FitnessBrowser__Smeli:SMc00676 SMc00676 amino acid-binding
           periplasmic signal peptide protein
          Length = 331

 Score =  350 bits (898), Expect = e-101
 Identities = 175/333 (52%), Positives = 224/333 (67%), Gaps = 2/333 (0%)

Query: 11  MTAAAVLGVSGFAQAGATLDAVQKKGFVQCGVSDGLPGFSVPDSTGKIVGIDADFCRAVA 70
           M   A   ++G     ATLD V+++G ++CGVS G+ GFS PD  G+  G D DFCRAVA
Sbjct: 1   MALFATAFLAGTTAQAATLDVVKQRGELRCGVSQGVLGFSAPDDKGEWSGFDIDFCRAVA 60

Query: 71  AAVFGDATKVKFSQLNAKERFTALQSGEIDMLSRNSTMTSSRDAGMGLKFPGFITYYDGI 130
           AA  G   KVK+  L+ KERFTALQSGE+D+LSR +T T SRD  +G+ F G + YYDG 
Sbjct: 61  AATLGSPDKVKYVPLSTKERFTALQSGEVDLLSRQTTWTLSRDTDLGMSFVG-VNYYDGQ 119

Query: 131 GFLANNKLGVKSAKELDGATICIQAGTTTELNVSDYFRANGLKYTPITFDTSDESAKSLE 190
            F+    +GVKS KEL GA++C + GTTTE N++DYF AN ++Y  I F+ +D++ ++  
Sbjct: 120 AFMVRGDIGVKSVKELSGASVCTETGTTTEQNMADYFSANKIEYQVIAFEKADQTIQAFN 179

Query: 191 SGRCDVLTSDKSQLFAQRSKLASPKDYVVLPETISKEPLGPVVRNGDDEWLAIVRWTGYA 250
           SGRCDV ++D S L++QR  L  P  +VVLPE ISKEPLGP VR GDD+W  +VRWT +A
Sbjct: 180 SGRCDVYSTDASALYSQRLTLNDPDRFVVLPEVISKEPLGPAVRQGDDQWFKVVRWTLFA 239

Query: 251 LLNAEEAGVTSKNVEAEAKSTKNPDVARMLGADGEYGKDLKLPKDWVVQIVKQVGNYGEM 310
           ++ AEE G+T +N  A    +      R LG D E GK L L   W  Q V  VGNYGE+
Sbjct: 240 MIEAEELGITRENA-ASLLESGTAAQKRFLGIDNEAGKALGLDPKWAYQTVAAVGNYGEI 298

Query: 311 FERNLGKGTPLEIDRGLNALWNAGGIQYAPPVR 343
           FER+LGK + L IDRGLN LWN GG+ YAPPVR
Sbjct: 299 FERHLGKESALRIDRGLNKLWNNGGLIYAPPVR 331


Lambda     K      H
   0.315    0.133    0.383 

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: 330
Number of extensions: 14
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: 343
Length of database: 331
Length adjustment: 28
Effective length of query: 315
Effective length of database: 303
Effective search space:    95445
Effective search space used:    95445
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 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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