GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tctC in Halomonas salina B6

Align Tricarboxylic transport TctC (characterized, see rationale)
to candidate WP_040183243.1 BN1003_RS00860 tripartite tricarboxylate transporter substrate binding protein

Query= uniprot:E4PJR1
         (328 letters)



>NCBI__GCF_000821105.2:WP_040183243.1
          Length = 331

 Score =  304 bits (779), Expect = 2e-87
 Identities = 155/329 (47%), Positives = 215/329 (65%), Gaps = 7/329 (2%)

Query: 6   IKRTLSFVAAAAVSMSAMAWQPSGKV----ECLAPADPGGGWDFTCRSVGNVLQDLGLVD 61
           IK     +AA+A+    +A    G      EC+APADPGGGWDFTCRSVG +L DL LVD
Sbjct: 4   IKHATRGLAASALLGLGLATSMPGHALPISECIAPADPGGGWDFTCRSVGKLLLDLELVD 63

Query: 62  GSVQTVNMAGAGGGVAYAHTVSKRAEDNKLLVAASTATTTRLAQKQFPGMNADMVTWVGA 121
             VQ  NM G  G VA+A+  S RA+D+ L+VA ST   T++AQ ++PG  AD + W+  
Sbjct: 64  SPVQVTNMPGGVGAVAFANVESNRADDSDLIVATSTVGITQIAQGRYPG-GADTMRWLAM 122

Query: 122 LGADYGIIAVGKNSEYQNLSELMAAVKANPKSVKFAGGSARGGWDHLKVLIAAKAAGA-- 179
           LG D G+I V  +SEYQ+L +L+  V  +P ++  AG S  GGWDH++ L+ AK AG   
Sbjct: 123 LGTDVGVILVDDDSEYQSLEQLLDTVVEDPGALAVAGSSGAGGWDHIRALMLAKEAGMPD 182

Query: 180 DKLPSIPYLSYNNGGEAMSQVVGGQVDAFTGDISEATGFLESGDLRVVAVLAEERLPGKF 239
           D++ S+ ++ ++ GG A++Q++GG VD  + D+ E  GF+ESGD+RV+AVL+EE LP  F
Sbjct: 183 DQIGSLRWVQFDGGGPAVTQMMGGHVDVVSTDLGEIAGFIESGDVRVLAVLSEEPLPEPF 242

Query: 240 SDLPTAKEQGIDAVGPNWRGFYMPKGASEEAKSYWVEAVDTLYASEEWKKVMKSNGLIPF 299
           +DLPTA  QG D  G NWRGFY     S+E  +  VE + TLY S+EWK+V + NGL+P 
Sbjct: 243 ADLPTAASQGYDVAGYNWRGFYTGGEVSDENYAAMVEDLKTLYDSDEWKEVAQQNGLVPL 302

Query: 300 HPPASQFDEFVRNQVQDIENLSREIGLLK 328
                 FD FVR  + ++E +SREIG+++
Sbjct: 303 WRGGDAFDAFVRESIDEVETISREIGVIQ 331


Lambda     K      H
   0.315    0.131    0.384 

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: 360
Number of extensions: 23
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: 328
Length of database: 331
Length adjustment: 28
Effective length of query: 300
Effective length of database: 303
Effective search space:    90900
Effective search space used:    90900
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 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