GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Rhodospirillum rubrum ATCC 11170

Align High-affinity branched-chain amino acid ABC transporter permease LivM (characterized, see rationale)
to candidate YP_428496.1 Rru_A3415 inner-membrane translocator

Query= uniprot:A0A159ZYE0
         (418 letters)



>NCBI__GCF_000013085.1:YP_428496.1
          Length = 295

 Score =  148 bits (373), Expect = 2e-40
 Identities = 102/304 (33%), Positives = 156/304 (51%), Gaps = 34/304 (11%)

Query: 116 IATLILIYVMLGLGLNIVVGLAGLLDLGYVGFYAVGAYSYALLSHYFGLSFWICLPIAGM 175
           +  + LIY ++ LGLN+  G  GL++ G VGF+A+GAY+ ALL    G    + LP A  
Sbjct: 8   VTVIALIYSLMTLGLNLQYGFTGLINFGVVGFFAIGAYTSALLV-VAGWPILLALPCAVA 66

Query: 176 MAATFGFLLGFPVLRLRGDYLAIVTLGFGEIIRLFLRNLTDITGGPNGISNIEKPTFFGL 235
            +A   + +    LRLR +Y AIV LGF E IRL + +   +TGG  G++ I        
Sbjct: 67  ASALVSWPVALLSLRLRIEYFAIVMLGFAETIRLVVTSEGWLTGGVQGVTGIPSLA---- 122

Query: 236 TFERKAAEGLQTFHEYFGLEYNSINKVIFLYLVALLLALAALFVINRLLRMPIGRAWEAL 295
                AA GL            S+   +   LVAL   +  +++  RL+  P GR   A+
Sbjct: 123 -----AALGL------------SMESTLLTALVALGAVIGVVWLSRRLVASPFGRIIRAI 165

Query: 296 REDEIACRALGLNPTVIKLSAFTLGAAFAGFAGSFFAARQGLVTPESFTFIESAIILAIV 355
           R+DE A +ALG  P   K++ F LG+A AG AG+ +A     ++P+ F  + +  I   +
Sbjct: 166 RDDEDAVQALGKAPGRFKVAVFVLGSASAGLAGALYAHYITYISPDQFMSLLTFYIWVAM 225

Query: 356 VLGGMGSQLGVILAAIVMILLPEMMR------------EFSEYRMLMFGALMVLMMIWRP 403
           +LGG+G   G +L   V+I L E  R            E +  R+ + G  ++++M +RP
Sbjct: 226 ILGGVGRVGGAVLGTAVLIGLMEGSRFLRDILPGVAEVEMASIRLGVIGLALMVLMRFRP 285

Query: 404 QGLL 407
           +GLL
Sbjct: 286 EGLL 289


Lambda     K      H
   0.331    0.145    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: 395
Number of extensions: 25
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: 418
Length of database: 295
Length adjustment: 29
Effective length of query: 389
Effective length of database: 266
Effective search space:   103474
Effective search space used:   103474
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 (21.9 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