GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Pseudomonas fluorescens FW300-N2E3

Align High-affinity branched-chain amino acid ABC transporter permease LivM (characterized, see rationale)
to candidate AO353_13535 AO353_13535 urea ABC transporter permease subunit UrtC

Query= uniprot:A0A159ZYE0
         (418 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_13535
          Length = 359

 Score =  105 bits (261), Expect = 3e-27
 Identities = 94/332 (28%), Positives = 149/332 (44%), Gaps = 56/332 (16%)

Query: 107 FFGSRGAVDIATLILIYVMLGLGLNIVVGLAGLLDLGYVGFYAVGAYSYALLS------- 159
           F  S   + +A  IL Y ++ L L++V G AGLL LG+  F+A+G Y+  +         
Sbjct: 44  FHVSAYTLTLAGKILCYAIVALALDLVWGYAGLLSLGHGLFFALGGYAMGMYLMRQASGD 103

Query: 160 ----------------HYFGLSFWI---CLPIA--GMMAATFGFLLGFPVLRLRGDYLAI 198
                           ++ G S +I   CL +   G++A  FGF       R++G Y +I
Sbjct: 104 GLPAFMTFLSWTELPWYWTGTSSFIWAMCLVVLAPGLLALVFGFFAFRS--RIKGVYFSI 161

Query: 199 VT--LGFGEIIRLFLRNLTDITGGPNGISNIEKPTFFGLTFERKAAEGLQTFHEYFGLEY 256
           +T  L F  ++ LF RN T   GG NG +N      FG+T     A              
Sbjct: 162 MTQALTFAGML-LFFRNETGF-GGNNGFTNFCTILGFGITEPGTRA-------------- 205

Query: 257 NSINKVIFLYLVALLLALAALFVINRLLRMPIGRAWEALREDEIACRALGLNPTVIKLSA 316
                   L++  +LL +A+LF+  RL +   GR   ALR+ E      G +P   KL  
Sbjct: 206 -------VLFVATVLLLVASLFIGWRLAQSKFGRVLTALRDAENRLMFCGYDPRGFKLFV 258

Query: 317 FTLGAAFAGFAGSFFAARQGLVTPESFTFIESAIILAIVVLGGMGSQLGVIL-AAIVMIL 375
           + L A   G AG+ +  + G++ P   +   S      V LGG G+ +G +L A +V  +
Sbjct: 259 WVLSAVLCGLAGALYVPQVGIINPSEMSPTNSIEAAVWVALGGRGTLIGPLLGAGVVNGM 318

Query: 376 LPEMMREFSEYRMLMFGALMVLMMIWRPQGLL 407
                  F EY +   GAL +++ ++ P+G++
Sbjct: 319 KSWFTVAFPEYWLFFLGALFIVVTLYLPKGVI 350


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: 453
Number of extensions: 23
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: 418
Length of database: 359
Length adjustment: 30
Effective length of query: 388
Effective length of database: 329
Effective search space:   127652
Effective search space used:   127652
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