GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Halococcus hamelinensis 100A6

Align High-affinity branched-chain amino acid ABC transporter permease LivM (characterized, see rationale)
to candidate WP_007692757.1 C447_RS08145 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A159ZYE0
         (418 letters)



>NCBI__GCF_000336675.1:WP_007692757.1
          Length = 397

 Score =  109 bits (272), Expect = 2e-28
 Identities = 92/324 (28%), Positives = 146/324 (45%), Gaps = 36/324 (11%)

Query: 99  IVGALVWPFFGSRGAVDIATLILIYV-MLGLGLNIVVGLAGLLDLGYVGFYAVGAYSYAL 157
           +V   V PF G      +  +   Y  M  +  + V G  G +  G+  F+AVG Y+  L
Sbjct: 43  VVAFAVLPFAGISTTQLLVLIGAFYFGMFAMSWDTVSGYTGEISFGHALFFAVGGYTSTL 102

Query: 158 LSHYFGLSFWICLPIAGMMAATFGFLLGFPVLRLRGDYLAIVTLGFGEIIRLFLRNLTDI 217
           L+  +G+S  + +P   ++AA  G L+G P LR+RG YL+++TL    I+        DI
Sbjct: 103 LNLGYGVSPGLSIPAGVVLAAVAGVLIGVPALRVRGPYLSLITLVAPLILLQVFVIYGDI 162

Query: 218 TGGPNGISNIEKPTFFGLTFERKAAEGLQTFHEYFGLEYNSINKVIFLYLVALLLALAAL 277
            GG  G+S               A  GL +  ++  +       V+  Y +   L LA +
Sbjct: 163 FGGELGLS---------------APTGLVSAPDFELV-------VLANYYIGFGLFLAIM 200

Query: 278 FVINRLLRMPIGRAWEALREDEIACRALGLNPTVIKLSAFTLGAAFAGFAGSFFAARQ-G 336
            ++  + R  +G    A+REDE A  A GLN    KL AF L AA  G AG+ F     G
Sbjct: 201 GLLFVVTRSDVGSVLTAVREDEDAVAAAGLNVAKFKLFAFVLSAAVGGLAGAVFVHTPIG 260

Query: 337 LVTPESFTFIESAI-ILAIVVLGGMGSQLGVILAAIVMILLPEMMRE-----------FS 384
              P     +  +I +L   +LGGMG+ +G  L  +      +++ +             
Sbjct: 261 SPRPSQLLALTVSIEVLIAAILGGMGTIVGAGLGGVFFYFFNDVLNQQGWTLPVLGVGVD 320

Query: 385 EYRMLMFGALMVLMMIWRPQGLLP 408
           E  +L+F  L ++++   PQG+ P
Sbjct: 321 EASLLIFVLLTMVVVYALPQGVFP 344


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: 475
Number of extensions: 38
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: 397
Length adjustment: 31
Effective length of query: 387
Effective length of database: 366
Effective search space:   141642
Effective search space used:   141642
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: 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