GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsA in Pseudovibrio axinellae Ad2

Align ABC transporter for D-Glucose-6-Phosphate, periplasmic substrate-binding component (characterized)
to candidate WP_068010535.1 PsAD2_RS21535 carbohydrate ABC transporter substrate-binding protein

Query= reanno::WCS417:GFF4324
         (428 letters)



>NCBI__GCF_001623255.1:WP_068010535.1
          Length = 415

 Score =  351 bits (900), Expect = e-101
 Identities = 183/397 (46%), Positives = 255/397 (64%), Gaps = 10/397 (2%)

Query: 11  ISIASLFPLSAFAADSKGTVEVVHWWTSGGEKAAVDVLKAQVEKDGFVWKDGAVAGGGGA 70
           +++A LF  S+  A +  T EV+H+WT+GGE  A   LK   E  G VW D  VAGGGG 
Sbjct: 9   VALAVLF--SSITAQAAPTAEVLHFWTAGGEARATRALKQAFEARGGVWDDAPVAGGGGD 66

Query: 71  TAMTVLKSRAVAGNPPGVAQIKGPDIQEWASTGLLDTDVLKDVAKEEKWDSLLDKKVSDT 130
               VL++R +A  PP + QIKG +IQEWA+ G L+   L   A+++ WD LL + + +T
Sbjct: 67  AMAAVLRARVLAKVPPSIVQIKGQNIQEWAAVGALEA--LDVTAQKQNWDKLLPELLKET 124

Query: 131 VKYEGDYVAVPVNIHRVNWLWINPEVFKKAGITKNPTTLQEFYAAGDKLKAAGFIPLAHG 190
           V+Y+G YVAVP+NIHRV+W+W NP+V  + G+T  P T  EF    DK+KAAG IPLAHG
Sbjct: 125 VQYQGKYVAVPLNIHRVDWIWANPKVLDQVGVTP-PQTWDEFNEVADKIKAAGIIPLAHG 183

Query: 191 GQPWQDSTVFEAVVLSVMGADGYKKALVDLDNGALTGPEMVKALTELKKVATYMDVDGKG 250
           GQPWQD T+FE V+L + GAD YKK  +DLD  AL    MVK   +++K++TY+D    G
Sbjct: 184 GQPWQDITLFEVVLLGIGGADFYKKVYLDLDQEALRSDTMVKVFDQMRKLSTYVDPGAPG 243

Query: 251 QDWNLEAGKVINGKAGMQIMGDWAKSEWTAAKKVAGKDYECVAFPGTDKAFTYNIDSLAV 310
           ++WNL    V+ G+A MQIMGDWAK+E+  A    G+D+ CV+ P +   +  N DS A+
Sbjct: 244 REWNLATAMVMRGEAAMQIMGDWAKAEFLTAGLKYGEDFICVSSP-SKGGYIINSDSFAM 302

Query: 311 FKQKDKGTAAGQQDIAKVVLGENFQKVFSINKGSIPVRNDMLNKMDSYGFDSCAQTAAKD 370
           FK  +    AGQQ +A ++L E  QK F++ KGSIP R  +   +D  GFD CA+ +++D
Sbjct: 303 FKISEPEQKAGQQLMASMLLDEQVQKDFNLLKGSIPARLGV--SLD--GFDECAKKSSED 358

Query: 371 FLADAKTGGLQPSMAHNMATTLAVQGAFFDVVTNYIN 407
            + +   G +  S+AH +  + AV+GAF DVVT + N
Sbjct: 359 LILNEARGTVVGSIAHELVQSGAVRGAFLDVVTEHFN 395


Lambda     K      H
   0.314    0.131    0.388 

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: 487
Number of extensions: 26
Number of successful extensions: 5
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: 428
Length of database: 415
Length adjustment: 32
Effective length of query: 396
Effective length of database: 383
Effective search space:   151668
Effective search space used:   151668
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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