GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Klebsiella michiganensis M5al

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate BWI76_RS06690 BWI76_RS06690 ABC transporter ATP-binding protein

Query= reanno::Smeli:SM_b21106
         (365 letters)



>FitnessBrowser__Koxy:BWI76_RS06690
          Length = 369

 Score =  323 bits (828), Expect = 5e-93
 Identities = 176/364 (48%), Positives = 236/364 (64%), Gaps = 19/364 (5%)

Query: 1   MAPVTLKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAI 60
           M+ + L+ + KR+G+   +H ++L+++D EF   VGPSGCGKST LRMIAGLEEVS G +
Sbjct: 1   MSNIRLRNVTKRFGSTVTLHQVNLDIEDGEFAVFVGPSGCGKSTLLRMIAGLEEVSEGEV 60

Query: 61  EIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAI 120
            IG   +ND+ P  R ++MVFQSYALYPHMTVAENMG+ LK+   P +EI+ +V   A  
Sbjct: 61  LIGDEVMNDVVPAHRGVAMVFQSYALYPHMTVAENMGYGLKVNKVPKDEIRRQVEMVAKT 120

Query: 121 LDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLH 180
           L L+HLL+R+P QLSGGQRQRVA+GRAIVR P VF+FDEPLSNLDA+LR ++R  I KLH
Sbjct: 121 LQLSHLLDRKPKQLSGGQRQRVAIGRAIVRNPRVFMFDEPLSNLDAELRVEMRLHIAKLH 180

Query: 181 ARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPMN 240
             ++ TM+YVTHDQVEAMTL+D+IV+M  G +EQ+G+P  ++  P  KFVAGFIGSP MN
Sbjct: 181 HELKTTMVYVTHDQVEAMTLADKIVVMNYGKVEQMGSPMSLYYNPVNKFVAGFIGSPKMN 240

Query: 241 MEEAVLT-------DGKLAFASGATLPLPPRFRSLVREGQKVTFGLRPDDVYPSGHGLHA 293
              A +T         K+A     TL +     S ++ G  VT G+RP+ +        +
Sbjct: 241 FLPATVTAWQPGQLSVKMAQDHNLTLNIT---TSPLQPGAAVTLGIRPEHL--------S 289

Query: 294 GDADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRML-NPRPLRPGEAVPMSFDLARA 352
            D +    +E    + E LGN T +F Q  G D V  +L      RP + + ++FD    
Sbjct: 290 TDVNIGTVVEFQCEVVERLGNNTYLFGQCYGHDNVKILLPGDVHFRPWQKISVAFDDRYC 349

Query: 353 HLFD 356
            +FD
Sbjct: 350 MVFD 353


Lambda     K      H
   0.320    0.137    0.397 

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: 370
Number of extensions: 18
Number of successful extensions: 2
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: 365
Length of database: 369
Length adjustment: 30
Effective length of query: 335
Effective length of database: 339
Effective search space:   113565
Effective search space used:   113565
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