GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12660 in Dinoroseobacter shibae DFL-12

Align D-lactate transporter, permease component 2 (characterized)
to candidate 3609311 Dshi_2696 inner-membrane translocator (RefSeq)

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



>FitnessBrowser__Dino:3609311
          Length = 554

 Score =  152 bits (384), Expect = 2e-41
 Identities = 99/326 (30%), Positives = 162/326 (49%), Gaps = 41/326 (12%)

Query: 11  GLDKGSAYALIALGLTLIFGTLGVVNFAHGALFMIGAFCAVTVQRVLSLSFETVDETQKD 70
           GL  GS   L A+GL + FG +GV+N AHG L MIGA+    VQ ++  SF         
Sbjct: 265 GLSLGSVLLLAAIGLAITFGVMGVINMAHGELVMIGAYTTFFVQEIIRTSF--------- 315

Query: 71  FLGNPLKVKTPYVESWFGPEVGGAIIDWAVPLAILFAIPIMIGVGYVMERGLIKHFYKRP 130
                     P+            + DW++ +A   A  +   VG  +ERG ++  Y RP
Sbjct: 316 ----------PH------------LFDWSLLIAAPLAFAVAGAVGVAIERGCVRFLYGRP 353

Query: 131 HADQILVTFGLAIVLQEVVKYFYGANPIQTPAPDALNGVVNLGSIIGMDIVYPVWRVVYF 190
             + +L T+G++++LQ+ V+  +G N  +   P  ++G   +G    M I Y   R+   
Sbjct: 354 -LETLLATWGISLILQQTVRSIFGPNNREVGNPSWMSGAFEVGQ---MTITYN--RLWIL 407

Query: 191 FFAVVIIGGIFSFLQFTTFGMVVRAGMADRETVGLLGINIDRRFTIMFGIAAAVAGLAGV 250
            FA+ +   +   L+ T  G+ +RA   +R     +GI       + FG+ A +AGLAGV
Sbjct: 408 LFALAVFAVLLFVLKKTAIGLQMRAVTQNRAMAANMGIRTGWVDAMTFGLGAGIAGLAGV 467

Query: 251 MYTPINSPNYHMGMDFLVLSFVVVVVGGMGSLPGAVLAGFLLGVLESFASMNEIKSLIPG 310
             + I++ + ++G  ++V SF+VVV GG G++ G + A F LG+   F  +      +  
Sbjct: 468 ALSQIDNVSPNLGQSYIVDSFMVVVFGGAGNIWGTLAAAFSLGIANKF--LEPYAGAV-- 523

Query: 311 IDQIIIYVVAIIILLTRPRGLMGRKG 336
           + +I++ V  I+ +  RPRGL   KG
Sbjct: 524 LAKILVLVFIILFIQKRPRGLFAVKG 549


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: 395
Number of extensions: 17
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 2
Length of query: 340
Length of database: 554
Length adjustment: 32
Effective length of query: 308
Effective length of database: 522
Effective search space:   160776
Effective search space used:   160776
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: 51 (24.3 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