GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12660 in Pseudomonas putida KT2440

Align D-lactate transporter, permease component 2 (characterized)
to candidate PP_4842 PP_4842 putative Urea ABC transporter

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



>FitnessBrowser__Putida:PP_4842
          Length = 495

 Score =  149 bits (376), Expect = 1e-40
 Identities = 104/341 (30%), Positives = 170/341 (49%), Gaps = 48/341 (14%)

Query: 4   ILLQILNGLDKGSAYALIALGLTLIFGTLGVVNFAHGALFMIGAFCAVTVQRVLSLSFET 63
           +L Q  +GL  GS   L ALGL + FG LGV+N AHG + M+GA+    VQ +L      
Sbjct: 199 LLGQAFSGLSLGSVLLLAALGLAITFGLLGVINMAHGEMLMLGAYSTYMVQVLLQR---- 254

Query: 64  VDETQKDFLGNPLKVKTPYVESWFGPEVGGAIIDWAVPLAILFAIPIMIGVGYVMERGLI 123
                                  F P      I++   +A+  A  +  GVG  +ER +I
Sbjct: 255 -----------------------FAP----GAIEFYPLIALPVAFAVSAGVGMALERTVI 287

Query: 124 KHFYKRPHADQILVTFGLAIVLQEVVKYFYGANPIQTPAPDALNGVVNLGSIIGMDIVYP 183
           +H Y RP  + +L T+G++++L + ++  +GA  ++   P  L+G + L      ++V P
Sbjct: 288 RHLYGRP-LETLLATWGISLILIQAIRLLFGAQNVEVSNPAWLSGGIQLLP----NLVLP 342

Query: 184 VWRVVYFFFAVVIIGGIFSFLQFTTFGMVVRAGMADRETVGLLGINIDRRFTIMFGIAAA 243
             R+V   FA+ ++   +  L  T  G+ VRA   +R      G++  R   + FG+ + 
Sbjct: 343 YNRLVIIGFALAVVLLTWLLLNRTRLGLNVRAVTQNRNMAACCGVSTGRVDMLAFGLGSG 402

Query: 244 VAGLAGVMYTPINSPNYHMGMDFLVLSFVVVVVGGMGSLPGAVLAGFLLGVLESFASMNE 303
           +AGL GV  + + +    +G  +++ SF+VVV+GG+G L G++ A F LG+         
Sbjct: 403 IAGLGGVALSQVGNVGPDLGQSYIIDSFLVVVLGGVGQLAGSLWAAFGLGIAN------- 455

Query: 304 IKSLIPGIDQII--IYVVAIIILL--TRPRGLMGRKGVMED 340
            K L P I  ++  I ++A+IIL    RP+GL   KG + D
Sbjct: 456 -KLLEPQIGAVLGKILILALIILFIQKRPQGLFALKGRVID 495


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: 357
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: 495
Length adjustment: 31
Effective length of query: 309
Effective length of database: 464
Effective search space:   143376
Effective search space used:   143376
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.

Links

Downloads

Related tools

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