GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5402 in Pseudomonas stutzeri RCH2

Align ABC transporter for D-Alanine, periplasmic substrate-binding component (characterized)
to candidate GFF3104 Psest_3163 ABC-type amino acid transport/signal transduction systems, periplasmic component/domain

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



>FitnessBrowser__psRCH2:GFF3104
          Length = 342

 Score =  548 bits (1413), Expect = e-161
 Identities = 271/340 (79%), Positives = 302/340 (88%), Gaps = 1/340 (0%)

Query: 4   LKSTLAVMTAAAVLGVSGFAQAGATLDAVQKKGFVQCGVSDGLPGFSVPDSTGKIVGIDA 63
           +KSTLAV+ AA++LG+SG AQAGATLDAVQKKGFVQCG+SDGLPGFS  D+ GK  GID 
Sbjct: 4   VKSTLAVLGAASLLGISGLAQAGATLDAVQKKGFVQCGISDGLPGFSFADAKGKYQGIDV 63

Query: 64  DFCRAVAAAVFGDATKVKFSQLNAKERFTALQSGEIDMLSRNSTMTSSRDAGMGLKFPGF 123
           D CRAVAAAVFGDA+KVK+S L AKERFTALQSGE+D+LSRN+T TSSRDA MGL F G 
Sbjct: 64  DICRAVAAAVFGDASKVKYSPLTAKERFTALQSGEVDVLSRNTTWTSSRDAAMGLNFTG- 122

Query: 124 ITYYDGIGFLANNKLGVKSAKELDGATICIQAGTTTELNVSDYFRANGLKYTPITFDTSD 183
           +TYYDG GFL N +LGV SAKELDGAT+CIQAGTTTELN+SDYFRANG KYTPIT+DTSD
Sbjct: 123 VTYYDGQGFLVNKELGVSSAKELDGATVCIQAGTTTELNLSDYFRANGHKYTPITYDTSD 182

Query: 184 ESAKSLESGRCDVLTSDKSQLFAQRSKLASPKDYVVLPETISKEPLGPVVRNGDDEWLAI 243
           ESAKSLESGRCDVLTSD+SQL+AQR KLA P DYVVLPE ISKEPLGP VR GD+EW  I
Sbjct: 183 ESAKSLESGRCDVLTSDQSQLYAQRIKLAKPADYVVLPEVISKEPLGPAVRQGDEEWFDI 242

Query: 244 VRWTGYALLNAEEAGVTSKNVEAEAKSTKNPDVARMLGADGEYGKDLKLPKDWVVQIVKQ 303
           VRWT +A+LNAEE GVTS NVE  AKSTKNPDVAR+LGA+GEYGKDLKLPKDW VQIVKQ
Sbjct: 243 VRWTLFAMLNAEELGVTSANVEEMAKSTKNPDVARLLGAEGEYGKDLKLPKDWAVQIVKQ 302

Query: 304 VGNYGEMFERNLGKGTPLEIDRGLNALWNAGGIQYAPPVR 343
           VGNYGE+F+RN+G G+ L+I+RGLNALWN GG+QYAPPVR
Sbjct: 303 VGNYGEIFDRNVGAGSELKIERGLNALWNNGGLQYAPPVR 342


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: 506
Number of extensions: 19
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: 343
Length of database: 342
Length adjustment: 29
Effective length of query: 314
Effective length of database: 313
Effective search space:    98282
Effective search space used:    98282
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.

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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