GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12660 in Pseudomonas simiae WCS417

Align D-lactate transporter, permease component 2 (characterized)
to candidate GFF556 PS417_02830 urea ABC transporter permease

Query= reanno::Phaeo:GFF1250
         (340 letters)



>FitnessBrowser__WCS417:GFF556
          Length = 500

 Score =  147 bits (372), Expect = 4e-40
 Identities = 105/341 (30%), Positives = 171/341 (50%), Gaps = 48/341 (14%)

Query: 4   ILLQILNGLDKGSAYALIALGLTLIFGTLGVVNFAHGALFMIGAFCAVTVQRVLSLSFET 63
           IL Q  +G+  GS   L ALGL + FG LGV+N AHG + M+GA+    VQ ++      
Sbjct: 204 ILGQAFSGMSLGSILLLAALGLAITFGLLGVINMAHGEMLMLGAYSTYMVQLLMQRYMPQ 263

Query: 64  VDETQKDFLGNPLKVKTPYVESWFGPEVGGAIIDWAVPLAILFAIPIMIGVGYVMERGLI 123
             E                    F P +       A+P+A      +   +G  +ER +I
Sbjct: 264 AIE--------------------FYPLI-------ALPVAFF----VTAAIGMALERTVI 292

Query: 124 KHFYKRPHADQILVTFGLAIVLQEVVKYFYGANPIQTPAPDALNGVVNLGSIIGMDIVYP 183
           +H Y RP  + +L T+G++++L ++V+  +GA  ++   P+ L+G V     +  ++V P
Sbjct: 293 RHLYGRP-LETLLATWGISLMLIQLVRLVFGAQNVEVSNPEWLSGGVQ----VLPNLVLP 347

Query: 184 VWRVVYFFFAVVIIGGIFSFLQFTTFGMVVRAGMADRETVGLLGINIDRRFTIMFGIAAA 243
             R+V   FA+ ++   +  L  T  G+ VRA   +R      G+   R   + FG+ + 
Sbjct: 348 YNRIVIIAFALCVVVLTWLLLNKTRLGLNVRAVTQNRNMAACCGVPTGRVDMLAFGLGSG 407

Query: 244 VAGLAGVMYTPINSPNYHMGMDFLVLSFVVVVVGGMGSLPGAVLAGFLLGVLESFASMNE 303
           +AGL GV  + I +    +G  +++ SF+VVV+GG+G L G+V+A F LG+         
Sbjct: 408 IAGLGGVALSQIGNVGPDLGQSYIIDSFLVVVLGGVGQLAGSVMAAFGLGIAN------- 460

Query: 304 IKSLIPGIDQII--IYVVAIIILL--TRPRGLMGRKGVMED 340
            K L P I  ++  I ++A+IIL    RP+GL   KG + D
Sbjct: 461 -KILEPQIGAVLGKILILALIILFIQKRPQGLFALKGRVID 500


Lambda     K      H
   0.329    0.147    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: 350
Number of extensions: 20
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 340
Length of database: 500
Length adjustment: 31
Effective length of query: 309
Effective length of database: 469
Effective search space:   144921
Effective search space used:   144921
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: 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