GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Dyella japonica UNC79MFTsu3.2

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  213 bits (542), Expect = 6e-60
 Identities = 134/353 (37%), Positives = 192/353 (54%), Gaps = 27/353 (7%)

Query: 1   MARISLDLAHSYKPNPQQDSDYALLPLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVP 60
           MA++ LD      PN        +     E  DG    L+GPSGCGKTT+L +++GL   
Sbjct: 1   MAKVRLDKLRKVYPN----GHVGVAEASFEIADGELLVLVGPSGCGKTTLLRMIAGLESI 56

Query: 61  SHGKVLFDGRDVTRASPQERNIAQVFQFPVIYDTMTVAENLAFPLRNRKVPEGQIKQRVG 120
           S G +    R V   +P++R+IA VFQ   +Y  MTVAENL F L+ R  P+ +I++RV 
Sbjct: 57  SGGTLSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLKLRGQPKAEIERRVA 116

Query: 121 VIAEMLEMSGQLNQRAAGLAADAKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRR 180
             A MLE+  +L+ R A L+   +Q+++LGR LVR D    L DEPL+ +D  L+  +R 
Sbjct: 117 EAARMLELEQRLDSRPAALSGGQRQRVALGRALVR-DPKVFLLDEPLSNLDAKLRLSMRV 175

Query: 181 KLKQIHHELKLTLIYVTHDQVEALTFADQVVVMTRGKAVQVGSADALFERPAHTFVGHFI 240
           ++ +IH  LK T++YVTHDQ+EA+T   ++VV+  G   Q+ +   L++ PA+ FV  F+
Sbjct: 176 EIARIHQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFL 235

Query: 241 GSPGMNFLPA--HRDGENLSVAGHRLASPVGR----ALPAGA---------LQVGIRPEY 285
           GSP MN L    +RDG      G +LA P G      LP GA         + VG+RPE 
Sbjct: 236 GSPAMNLLRGILYRDG------GWKLAMPQGELVLGELPQGAALEAWRDRDIVVGLRPED 289

Query: 286 LALAQPQQAGALPGTVVQVQDIGTYQMLTAKVGEHTVKARFTPETRLPSSGDT 338
           L L       AL   +  V+ +G    L  + GE  + +R  P   LP+ G T
Sbjct: 290 LLLCADAAGAALAAQLEVVEPVGNEVFLNLRHGELALVSRMPPR-ELPAPGST 341


Lambda     K      H
   0.320    0.136    0.395 

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: 297
Number of extensions: 15
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: 358
Length of database: 364
Length adjustment: 29
Effective length of query: 329
Effective length of database: 335
Effective search space:   110215
Effective search space used:   110215
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 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