GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Klebsiella michiganensis M5al

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate BWI76_RS06690 BWI76_RS06690 ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__Koxy:BWI76_RS06690
          Length = 369

 Score =  310 bits (793), Expect = 5e-89
 Identities = 165/359 (45%), Positives = 233/359 (64%), Gaps = 11/359 (3%)

Query: 1   MTSVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQI 60
           M+++ +R+++  FG+   L ++NLDI+ GEF V +G SGCGKSTLL  IAGL +VS+G++
Sbjct: 1   MSNIRLRNVTKRFGSTVTLHQVNLDIEDGEFAVFVGPSGCGKSTLLRMIAGLEEVSEGEV 60

Query: 61  FIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEI 120
            I D  +    P  RG+ MVFQSYALYP MTV +N+ +GLKV K+P  EI ++V+  ++ 
Sbjct: 61  LIGDEVMNDVVPAHRGVAMVFQSYALYPHMTVAENMGYGLKVNKVPKDEIRRQVEMVAKT 120

Query: 121 LQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLH 180
           LQ+  LL RKP +LSGGQRQRVAIGRA+VR+  VF+FDEPLSNLDA+LR E+R+ I +LH
Sbjct: 121 LQLSHLLDRKPKQLSGGQRQRVAIGRAIVRNPRVFMFDEPLSNLDAELRVEMRLHIAKLH 180

Query: 181 QSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMN 240
             LK TM+YVTHDQ+EA+TLAD+I VM  G ++Q+  PM++Y  P N FVAGFIGSP MN
Sbjct: 181 HELKTTMVYVTHDQVEAMTLADKIVVMNYGKVEQMGSPMSLYYNPVNKFVAGFIGSPKMN 240

Query: 241 FFRGEVEP-KDGRSFVRAG---GIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDG 296
           F    V   + G+  V+      +  ++T  P    LQPG  V LG+RPEH+  D     
Sbjct: 241 FLPATVTAWQPGQLSVKMAQDHNLTLNITTSP----LQPGAAVTLGIRPEHLSTDVNIGT 296

Query: 297 EPTHQAVVDIEEPMGADNLLW-LTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASIFD 354
               Q   ++ E +G +  L+   +   ++ + + G   + P   + ++FD     +FD
Sbjct: 297 VVEFQC--EVVERLGNNTYLFGQCYGHDNVKILLPGDVHFRPWQKISVAFDDRYCMVFD 353


Lambda     K      H
   0.320    0.137    0.392 

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: 362
Number of extensions: 15
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: 361
Length of database: 369
Length adjustment: 30
Effective length of query: 331
Effective length of database: 339
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 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