GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Sinorhizobium meliloti 1021

Align High-affinity branched-chain amino acid transport system permease protein BraD, component of Branched chain amino acid uptake transporter. Transports alanine (characterized)
to candidate SMc02359 SMc02359 high-affinity branched-chain amino acid ABC transporter permease

Query= TCDB::P21627
         (307 letters)



>FitnessBrowser__Smeli:SMc02359
          Length = 296

 Score =  156 bits (394), Expect = 6e-43
 Identities = 93/301 (30%), Positives = 165/301 (54%), Gaps = 21/301 (6%)

Query: 8   LQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGLDS 67
           +Q +++ L++G  YAL+A+G  ++YGI+ ++NFA+GE+ M+  Y  F+A           
Sbjct: 5   IQFVIDVLSLGGAYALMALGLVIIYGILRLVNFAYGELIMVAGYTMFLASG-------SG 57

Query: 68  VPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAVMLSQDS 127
           +P +++A  A  + +   FG   +  A+RP+R  +    LI++   S  LQNA +L    
Sbjct: 58  LPWIVMAVLAVGMAIL--FGIITDYAAFRPVRAKSVTAVLITSFAFSNLLQNAALLFISP 115

Query: 128 KEKAIPTLLPGNFVFGES-SMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRAC 186
           + + +P  LP   +F ++ S+ G +     ++    +  ++ G+   + R+ LG A RA 
Sbjct: 116 RPRNVP--LPD--IFSQTVSIGGAITPVRNLITIAASIALLAGVAFLMRRTTLGIAMRAA 171

Query: 187 AEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAAV 246
           A +  M  +LG+ +N II+  F +   LA V  +L   + G + PGIG    + AF A V
Sbjct: 172 ATNFTMARMLGVPANLIISSAFALSGFLAGVVGILWIGRIGTVVPGIGLEPLLVAFIATV 231

Query: 247 LGGIGSIPGAMLGGLLLGVAE-----AFGADVFGDQYKDVVAFGLLILVLLFRPTGILGR 301
           +GG+ S+PGA++GG LL + +         D+   +++D   F L+IL+LL+RP G++  
Sbjct: 232 IGGMRSLPGAVVGGFLLALIDTTLNYTLSQDLL--KFRDAFTFSLVILILLWRPDGLIRG 289

Query: 302 P 302
           P
Sbjct: 290 P 290


Lambda     K      H
   0.328    0.145    0.413 

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: 276
Number of extensions: 17
Number of successful extensions: 4
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: 307
Length of database: 296
Length adjustment: 27
Effective length of query: 280
Effective length of database: 269
Effective search space:    75320
Effective search space used:    75320
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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