GapMind for catabolism of small carbon sources

 

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

Align ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

Query= BRENDA::P68187
         (371 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  317 bits (811), Expect = 4e-91
 Identities = 182/374 (48%), Positives = 239/374 (63%), Gaps = 23/374 (6%)

Query: 1   MASVQLQNVTKAW--GEVVVSKDINLDIHEGEFVVFVGPSGCGKSTLLRMIAGLETITSG 58
           MA V+L  + K +  G V V+ + + +I +GE +V VGPSGCGK+TLLRMIAGLE+I+ G
Sbjct: 1   MAKVRLDKLRKVYPNGHVGVA-EASFEIADGELLVLVGPSGCGKTTLLRMIAGLESISGG 59

Query: 59  DLFIGEKRMNDTPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVINQRVNQVA 118
            L IGE+ +ND  P +R + MVFQ+YALYPH++VAEN+ FGLKL G  K  I +RV + A
Sbjct: 60  TLSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLKLRGQPKAEIERRVAEAA 119

Query: 119 EVLQLAHLLDRKPKALSGGQRQRVAIGRTLVAEPSVFLLDEPLSNLDAALRVQMRIEISR 178
            +L+L   LD +P ALSGGQRQRVA+GR LV +P VFLLDEPLSNLDA LR+ MR+EI+R
Sbjct: 120 RMLELEQRLDSRPAALSGGQRQRVALGRALVRDPKVFLLDEPLSNLDAKLRLSMRVEIAR 179

Query: 179 LHKRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPK 238
           +H+RL  TM+YVTHDQ+EAMTL  +IVVL+ G + Q+  P+ LY  PA+ FVAGF+GSP 
Sbjct: 180 IHQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFLGSPA 239

Query: 239 MNFL--------PVKVTATAIDQVQVELPMPNRQQVWLPVESRDVQVGANMSLGIRPEH- 289
           MN L          K+     + V  ELP     + W     RD+ V      G+RPE  
Sbjct: 240 MNLLRGILYRDGGWKLAMPQGELVLGELPQGAALEAW---RDRDIVV------GLRPEDL 290

Query: 290 LLPSDIADVILEGEVQVVEQLGNETQIHIQIPSIRQNLVYRQNDVVLVEEGATFAIGLPP 349
           LL +D A   L  +++VVE +GNE  ++++   +   LV R     L   G+T   G  P
Sbjct: 291 LLCADAAGAALAAQLEVVEPVGNEVFLNLRHGELA--LVSRMPPRELPAPGSTLHFGFAP 348

Query: 350 ERCHLFREDGTACR 363
           ER H F   G   R
Sbjct: 349 ERLHFFDAKGEGAR 362


Lambda     K      H
   0.320    0.137    0.393 

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: 393
Number of extensions: 19
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: 371
Length of database: 364
Length adjustment: 30
Effective length of query: 341
Effective length of database: 334
Effective search space:   113894
Effective search space used:   113894
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