GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08240 in Desulfovibrio vulgaris Hildenborough

Align Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale)
to candidate 209488 DVU0549 high-affinity branched-chain amino acid ABC transporter, permease protein

Query= uniprot:G8ALI9
         (505 letters)



>MicrobesOnline__882:209488
          Length = 407

 Score =  313 bits (802), Expect = 7e-90
 Identities = 173/351 (49%), Positives = 226/351 (64%), Gaps = 22/351 (6%)

Query: 140 IAAQVQHASRWLGPIAVVVALAFPFTP-LADRQLLDIGILLLTYIMLGWGLNIVVGLAGL 198
           + A+V+  +R   P  + V + F   P L      +I I  L Y+MLG GLNIVVGL+G 
Sbjct: 78  LMARVRSDARLRTPALLAVLVVFAVLPMLVSTYQTNIMISALLYVMLGLGLNIVVGLSGQ 137

Query: 199 LDLGYVAFYAVGAYSYALLAHYFGFSFWVCLPLAGFLAAMSGVLLGFPVLRLRGDYFAIV 258
           L LGYVAFYAVGAY+YALL   FG  FW  LP+ G LAA+ G+LLGFPVLRL+GDY AIV
Sbjct: 138 LVLGYVAFYAVGAYAYALLNADFGLGFWTVLPIGGALAAVFGILLGFPVLRLKGDYLAIV 197

Query: 259 TLGFGEIIRIILINWYQFTGGPNGISGIPRPSFFGIADFTRTPAEGTAAFHEMFGLEFSP 318
           TLGFGEI+R++L NW   T GP+GIS I RP                     +FG+E S 
Sbjct: 198 TLGFGEIVRLVLENWGSVTRGPSGISKIARPG--------------------LFGMELSV 237

Query: 319 LHRIIFLYYLILVLALVVNLFTMRVRKLPLGRAWEALREDDIACASLGINRTNMKLAAFA 378
                ++YYLIL   +       R++   +GRAW+ALRED+IAC ++GI+ T  KL AFA
Sbjct: 238 SEATTYIYYLILAAVIFTIFAVGRLKDSRIGRAWQALREDEIACEAMGIDLTTTKLTAFA 297

Query: 379 IAAMFGGFAGSFFATRQGFISPESFTFIESAIILAIVVLGGMGSQIGVVVAAFLVIGLPE 438
           + A + GFAG  FA +  FI+P SFTF+ESA+ILA+VVLGGMGS +GVV+ A ++I LPE
Sbjct: 298 LGACWAGFAGVIFAAKTTFINPASFTFLESAMILAMVVLGGMGSTLGVVLGALVLILLPE 357

Query: 439 AFRELADYRMLAFGMGMVLIMLWRPRGLLAHRDPTILLHGRPKGGAGGPAA 489
             R  ++YRML FG  MVL+M++RP+GL++ R     ++  P+ G  G  A
Sbjct: 358 YLRAFSEYRMLIFGAAMVLMMVFRPQGLVSCRSREYDVND-PEAGKSGEKA 407


Lambda     K      H
   0.329    0.144    0.438 

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: 558
Number of extensions: 29
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: 505
Length of database: 407
Length adjustment: 33
Effective length of query: 472
Effective length of database: 374
Effective search space:   176528
Effective search space used:   176528
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: 51 (24.3 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