GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Azospirillum thiophilum BV-S

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_045580995.1 AL072_RS06645 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_001305595.1:WP_045580995.1
          Length = 315

 Score =  175 bits (443), Expect = 2e-48
 Identities = 108/320 (33%), Positives = 176/320 (55%), Gaps = 34/320 (10%)

Query: 93  LVALLVLAVAWPFMVSRGTVDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYAIGAYT 152
           +V    +AV   F+ +   +DIA L     ++ +GLN+++G +G + LG+ GF+ IGAY 
Sbjct: 13  MVLAAAIAVLPAFLPNNFYLDIAILAGFNAVVCVGLNLLIGYAGQISLGHAGFFGIGAYA 72

Query: 153 FALLNHYYGLGFWTCLPIAGLMAAAA-----GFLLGFPVLRLRGDYLAIVTLGFGEIVRI 207
             +L   YG   W   P+  L+A AA      F +  P+LRL+G YLA+ TLG G IV I
Sbjct: 73  SGVLVGTYG---WP--PVLALLAGAAVVGLLAFAVAKPILRLKGHYLAMATLGIGIIVSI 127

Query: 208 LLLNNTEITGGPNGISQIPKPTLFGLEFSRTAREGGWDTFSNFFGLKYDPSDRVIFLYLV 267
           +L   + +TGGP+G+   P   +FG+E                +G K       ++ ++V
Sbjct: 128 VLRTESGLTGGPDGMMVEPF-RIFGIEL---------------YGEK-------VWYWVV 164

Query: 268 ALLLVVLSLFVINRLLRMPLGRAWEALREDEIACRSLGLSPRRIKLTAFTISAAFAGFAG 327
            +LLV +    +N L+  P+GRA  A+   E+A   +G+   R K+  F +SA FA  AG
Sbjct: 165 GVLLVGVVWLSLN-LIDSPMGRALRAVHGSEVAAEVVGVDTARFKVLVFVLSAVFASVAG 223

Query: 328 TLFAARQGFVSPESFTFAESAFVLAIVVLGGMGSQFAVILAAILLVVSRELMRDFNEYSM 387
           +LFA   G ++P    F +S  ++ +VV GGM S F  ++ A++L +  + +  F +Y  
Sbjct: 224 SLFAHYAGLITPAKADFFKSIELVTMVVFGGMASTFGAVVGAVVLTLLPQALTMFQDYQQ 283

Query: 388 LMLGGLMVLMMIWRPQGLLP 407
           ++LGG+++  M++ P+GLLP
Sbjct: 284 IVLGGILMATMVFMPKGLLP 303


Lambda     K      H
   0.330    0.145    0.436 

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: 301
Number of extensions: 11
Number of successful extensions: 2
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: 425
Length of database: 315
Length adjustment: 30
Effective length of query: 395
Effective length of database: 285
Effective search space:   112575
Effective search space used:   112575
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 (21.8 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