GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Dinoroseobacter shibae DFL-12

Align High-affinity branched-chain amino acid ABC transporter permease LivM (characterized, see rationale)
to candidate 3606951 Dshi_0379 inner-membrane translocator (RefSeq)

Query= uniprot:A0A159ZYE0
         (418 letters)



>FitnessBrowser__Dino:3606951
          Length = 358

 Score =  141 bits (356), Expect = 3e-38
 Identities = 101/331 (30%), Positives = 167/331 (50%), Gaps = 37/331 (11%)

Query: 93  WIVLALIVGALVWPF-FGSRGAVDIATLILIYVMLGLGLNIVVGLAGLLDLGYVGFYAVG 151
           ++VLA+ VG +  PF      A  +    LI+ +  +GLNI+ G  G + LG  GF AVG
Sbjct: 30  YLVLAVAVGII--PFVINDYWASAVMVPFLIWAIAAIGLNILTGYCGQVSLGTGGFMAVG 87

Query: 152 AYS-YALLSHYFGLSFWICLPIAGMMAATFGFLLGFPVLRLRGDYLAIVTLGFGE-IIRL 209
           AY+ Y L++ +  L+  IC+ + G++ A  G L G P LR++G YLA+ TL     ++ L
Sbjct: 88  AYACYKLMTAFPDLNIAICVLLGGVITAAVGVLFGLPSLRIKGFYLAVATLAAQFFLVWL 147

Query: 210 FLRNLTDITGGPNGISNIEKPTFFGLTFERKAAEGLQTFHEYFGLEYNSINKVIFLYLVA 269
           F +         +G  N  + T FG       A+    +                L+ +A
Sbjct: 148 FNKVPWFYNYSASGQINAPERTMFGYAITGPNADAAPKY----------------LFCLA 191

Query: 270 LLLALAALFVINRLLRMPIGRAWEALREDEIACRALGLNPTVIKLSAFTLGAAFAGFAGS 329
            L  LA  ++   L R  IGR+W A+R+ +IA   +G+NP   KL+AF + + F G AG+
Sbjct: 192 FLFVLA--WLARNLTRGTIGRSWMAIRDMDIAAEIIGVNPLKAKLTAFAVSSFFVGVAGA 249

Query: 330 -FFAARQGLV-TPESFTFIESAIILAIVVLGGMGSQLGVILAAIVMILLPEMMREF---- 383
            FF+   G V   E+F   +S ++L ++++GG+GS  G +  A  ++LLP +++      
Sbjct: 250 LFFSVYLGAVEVGEAFGINQSFLVLFMIIIGGLGSIFGSLAGAAFIVLLPVLLKNVMVGS 309

Query: 384 --------SEYRMLMFGALMVLMMIWRPQGL 406
                   + +  ++ G L++  +I  P GL
Sbjct: 310 LGWDTAIAAHFEFVVLGGLIIFFLIVEPHGL 340


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: 463
Number of extensions: 26
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: 358
Length adjustment: 30
Effective length of query: 388
Effective length of database: 328
Effective search space:   127264
Effective search space used:   127264
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 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