GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braE in Marinobacter adhaerens HP15

Align High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine (characterized)
to candidate GFF4157 HP15_4097 inner-membrane translocator

Query= TCDB::P21628
         (417 letters)



>FitnessBrowser__Marino:GFF4157
          Length = 347

 Score =  164 bits (415), Expect = 4e-45
 Identities = 108/332 (32%), Positives = 161/332 (48%), Gaps = 39/332 (11%)

Query: 90  TQRWAVLALVVVAFVWPFFASRGAVDIATLILIYVMLGIGLNIVVGLAGLLDLGYVGFYA 149
           TQ+  +   +++  V+PF      + +  L+ I V+   GLNI+ G  GL+ LG  GF  
Sbjct: 21  TQKLWLGFFLLILLVFPFVVDSYLLYLGCLVGIAVISTTGLNILTGFTGLISLGQAGFMG 80

Query: 150 VGAYTYALLAEYAGFGFWTALPIAGMMAALFGFLLGFPVLRLRGDYLAIVTLGFGEIIRI 209
           VGAYT A L+      F   L +AG+MAA  G L+G P LR++G YLAI TL     +  
Sbjct: 81  VGAYTVAWLSINTALPFPVTLVLAGLMAAAVGILVGLPSLRVKGLYLAIATLAASVFLHF 140

Query: 210 LLRNMTEITGGPNGIGSIPKPTLFGLTFERRAPEGMQTFHEFFGIAYNTNYKVILLYVVA 269
           +      +TGG  G+ S+    LFGLTF+                         ++Y + 
Sbjct: 141 IFAEWESVTGGMGGL-SLEPAHLFGLTFQ----------------------SDFMMYFII 177

Query: 270 LLLVLLALFVINRLMRMPIGRAWEALREDEVACRALGLNPTIVKLSAFTIGASFAGFAGS 329
           + L +L +     + R  IGRA+ A+R+ +++   LG+N    KL +F + + +AG AG 
Sbjct: 178 VPLAVLMVLAARNVFRTRIGRAFIAIRDRDISAEILGINLLRYKLMSFALSSFYAGIAGG 237

Query: 330 FFAARQGLVTPESFTFIESAMILAIVVLGGMGSQLGVILAAVVMVLLQEMRG-------- 381
            FA    +VTPESF    S   LA V++GGMG+ LG IL A  M L+ E           
Sbjct: 238 LFAYFYRVVTPESFPLSMSIFYLAAVIVGGMGNLLGGILGAAFMTLVPEALKLLTAALTP 297

Query: 382 --------FNEYRMLIFGLTMIVMMIWRPQGL 405
                    +    +IFG  ++  +I+ P GL
Sbjct: 298 FYPNAPVFMSPMLEIIFGALIVGFLIFEPHGL 329


Lambda     K      H
   0.330    0.146    0.439 

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: 428
Number of extensions: 33
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: 417
Length of database: 347
Length adjustment: 30
Effective length of query: 387
Effective length of database: 317
Effective search space:   122679
Effective search space used:   122679
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 50 (23.9 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:

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