GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Echinicola vietnamensis KMM 6221, DSM 17526

Align Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate Echvi_2123 Echvi_2123 ABC-type spermidine/putrescine transport systems, ATPase components

Query= SwissProt::P19566
         (369 letters)



>FitnessBrowser__Cola:Echvi_2123
          Length = 318

 Score =  151 bits (381), Expect = 3e-41
 Identities = 102/320 (31%), Positives = 173/320 (54%), Gaps = 35/320 (10%)

Query: 1   MASVQLRNVTKAW-GDVVVSKDINLDIHDGEFVVFVGPSGCGKSTLLRMIAGLETITSGD 59
           M+ +++  V+K +    +  +D +L +  G  V  VG SG GKS+LLR+IAGLE  ++G 
Sbjct: 1   MSYLKVSEVSKRYDAGSLALEDFSLQVKRGGVVSMVGESGSGKSSLLRIIAGLEVQSAGV 60

Query: 60  LFIGETRM----NDIPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVMNQRVN 115
           + +G+ ++      + P    + ++ Q Y LYP+ +V EN++  L L    K    +R  
Sbjct: 61  VHLGDQKILNPAQKLVPGYDEIQLIHQEYKLYPNSTVEENIARPLLLYD--KAYQKERTA 118

Query: 116 QVAEVLQLAHLLERKPKALSGGQRQRVAIGRTLVAEPRVFLLDEPLSNLDAALRVQMRIE 175
           ++ E+L L    ++KP+ LSGGQ+Q+VAIGR L  EP V LLDEP S+LDA  +  +  E
Sbjct: 119 EILELLSLRAFKDKKPRQLSGGQQQKVAIGRALSIEPEVLLLDEPFSSLDAIQKRDLIEE 178

Query: 176 ISRLHKRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIG 235
           +  +   L  T+I+VTHD  +A+ ++++++++  G++ Q G   E++  PA  +VA   G
Sbjct: 179 LKEIFDALEVTVIFVTHDVDDALLMSEELLIIQKGKLLQQGNVREVFRKPASAYVARLFG 238

Query: 236 SPKMNFLP-----------VKVT------ATAIEQ--------VQVELPNRQQIW-LPVE 269
              +N +P           VK+T      A  ++Q        + V+L + +  W +   
Sbjct: 239 --YLNLIPGAEEAYVRPSEVKITSKTSIKAEVVKQQFLIHYNLLTVKLEDSELFWKVDDP 296

Query: 270 SRGVQVGANMSLGIRPEHLL 289
           SR V VG  + L  + E L+
Sbjct: 297 SRSVNVGDEVFLDYQKEQLI 316


Lambda     K      H
   0.321    0.138    0.396 

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: 199
Number of extensions: 6
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: 369
Length of database: 318
Length adjustment: 29
Effective length of query: 340
Effective length of database: 289
Effective search space:    98260
Effective search space used:    98260
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