GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Desulfovibrio vulgaris Hildenborough

Align High-affinity branched-chain amino acid ABC transporter permease LivM (characterized, see rationale)
to candidate 206139 DVU0714 branched-chain amino acid ABC transporter, permease protein

Query= uniprot:A0A159ZYE0
         (418 letters)



>MicrobesOnline__882:206139
          Length = 317

 Score =  229 bits (584), Expect = 9e-65
 Identities = 127/314 (40%), Positives = 191/314 (60%), Gaps = 26/314 (8%)

Query: 96  LALIVGALVWPFFGSRGAVDIATLILIYVMLGLGLNIVVGLAGLLDLGYVGFYAVGAYSY 155
           LA+++  L  P F      D+   I +Y +L L LN+++G AGL  +G+  FYAVGAY+ 
Sbjct: 11  LAVLIAVL--PLFLDPYWTDVCVSIGLYAVLALSLNLILGQAGLFHMGHAAFYAVGAYTA 68

Query: 156 ALLSHYFGLSFWICLPIAGMMAATFGFLLGFPVLRLRGDYLAIVTLGFGEIIRL-FLRNL 214
           A+L+  + +     +P+AG++AA F  ++  P++ LRGDYL IVT+G  EI+R+  + N+
Sbjct: 69  AILNTVYHVPVLWTMPVAGLLAALFALVVARPIIHLRGDYLLIVTIGIVEIVRIALINNV 128

Query: 215 TDITGGPNGISNIEKPTFFGLTFERKAAEGLQTFHEYFGLEYNSINKVIFLYLVALLLAL 274
             ITGG NGI  I +P  FG                     Y     + F YL+   +A+
Sbjct: 129 FGITGGANGIFGISRPMLFG---------------------YKISKPIQFYYLIWTWVAI 167

Query: 275 AALFVINRLLRMPIGRAWEALREDEIACRALGLNPTVIKLSAFTLGAAFAGFAGSFFAAR 334
           + L +  RL     GRA   ++ED++A    G++    KL+AF LGA +AG  G+F+AA+
Sbjct: 168 SIL-LFRRLECSRFGRALNYIKEDDVAAEGSGVDTAYYKLAAFVLGALWAGMTGTFYAAK 226

Query: 335 QGLVTPESFTFIESAIILAIVVLGGMGSQLGVILAAIVMILLPEMMREFSEYRMLMFGAL 394
             +++PESF+F ES ++ AIV+LGG GS  GV+L A ++I LPE+ R+F+  RML+FG  
Sbjct: 227 MTIISPESFSFWESVVLFAIVILGG-GSNRGVLLGAFLLIGLPELFRDFASARMLIFGLA 285

Query: 395 MVLMMIWRPQGLLP 408
           MV+MMI+RPQG+LP
Sbjct: 286 MVVMMIFRPQGMLP 299


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: 413
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: 418
Length of database: 317
Length adjustment: 29
Effective length of query: 389
Effective length of database: 288
Effective search space:   112032
Effective search space used:   112032
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 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