GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Tistlia consotensis USBA 355

Align Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate WP_085123761.1 B9O00_RS16330 ABC transporter ATP-binding protein

Query= SwissProt::P19566
         (369 letters)



>NCBI__GCF_900177295.1:WP_085123761.1
          Length = 361

 Score =  317 bits (812), Expect = 3e-91
 Identities = 175/370 (47%), Positives = 239/370 (64%), Gaps = 18/370 (4%)

Query: 1   MASVQLRNVTKAWGDVVVS-KDINLDIHDGEFVVFVGPSGCGKSTLLRMIAGLETITSGD 59
           M SV+ +++ KA+GD  V+ +D +L++ DGEF+ F+GPSGCGK+T LRM AGLET TSG+
Sbjct: 1   MVSVRYQHLHKAFGDGSVALQDFSLEVADGEFLTFLGPSGCGKTTTLRMTAGLETPTSGE 60

Query: 60  LFIGETRMNDIPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVMNQRVNQVAE 119
           +F GE  + D+PP  R + MVFQSYALYPH++V +N+ + L+  G  ++   +R   +A 
Sbjct: 61  IFFGERPVVDLPPGRRNIAMVFQSYALYPHMTVQQNLEYPLRKQGVARDERARRATALAA 120

Query: 120 VLQLAHLLERKPKALSGGQRQRVAIGRTLVAEPRVFLLDEPLSNLDAALRVQMRIEISRL 179
            LQL  LL R+PK LSGGQ+QRVA+GR L+ EP VFLLDEPLSNLDA LR QMR E+ +L
Sbjct: 121 TLQLDALLHRRPKHLSGGQQQRVALGRALIREPEVFLLDEPLSNLDAELRTQMRAELIQL 180

Query: 180 HKRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKM 239
           H+R+GRTMIYVTHDQVEAMT++ +I V+  G + QVG PLE+Y  P +RFVA F+GSP M
Sbjct: 181 HRRIGRTMIYVTHDQVEAMTMSTRIAVMSKGELQQVGTPLEIYREPRNRFVAAFVGSPAM 240

Query: 240 NFLPVKV------TATAIEQVQVELPNRQQIWLPVESRGVQVGANMSLGIRPEHLLPSDI 293
           NF+   +             ++V LP+ +   L     G+   + +  GIRPEHL    +
Sbjct: 241 NFVEGGIELRDGRAVFRAAGLEVALPDARSARL----AGLARASGVLAGIRPEHL---SL 293

Query: 294 ADVTLEGEVQVVEQLGHETQIHIQIPAIRQNLVYRQNDVVLVEEGATFAIGLPPERCHLF 353
              + EG V VVE +GHE  +  + PA R  +V R         G    + + PE+ HLF
Sbjct: 294 EPGSGEGRVLVVEAMGHEDIVTAETPAGR--IVVRSAGTATAAAGDLVPLRVDPEKLHLF 351

Query: 354 REDGSACRRL 363
             D ++  RL
Sbjct: 352 --DAASGERL 359


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: 373
Number of extensions: 11
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: 361
Length adjustment: 30
Effective length of query: 339
Effective length of database: 331
Effective search space:   112209
Effective search space used:   112209
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 Apr 09 2024. 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