GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Sm in Sinorhizobium meliloti 1021

Align MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized)
to candidate SMc03065 SMc03065 alpha-glucoside ABC transporter ATP-binding protein

Query= TCDB::Q8DT25
         (377 letters)



>FitnessBrowser__Smeli:SMc03065
          Length = 362

 Score =  311 bits (796), Expect = 2e-89
 Identities = 186/378 (49%), Positives = 240/378 (63%), Gaps = 33/378 (8%)

Query: 1   MTTLKLDNIYKRYPNAKHYSVENFNLDIHDKEFIVFVGPSGCGKSTTLRMIAGLEDITEG 60
           MT L L +I K Y       +   +LDI + EF+VFVGPSGCGKST LRMIAGLE+IT G
Sbjct: 1   MTGLLLKDIRKSYGAVD--VIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGG 58

Query: 61  NLYIDDKLMNDASPKDRDIAMVFQNYALYPHMSVYENMAFGLKLRKYKKDDINKRVHEAA 120
           +++ID + +ND  P  R IAMVFQ+YALYPHM+VY+NMAFG+++ +  K++I++RV  AA
Sbjct: 59  DMFIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAA 118

Query: 121 EILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVAMRAEIAK 180
           ++L LT +L+R P  LSGGQRQRVA+GRAI R+ KVFL DEPLSNLDA LRVA R EIAK
Sbjct: 119 DMLQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAK 178

Query: 181 IHRRIGATT-IYVTHDQTEAMTLADRIVIMSATPNPDKTGSIGRIEQIGTPQELYNEPAN 239
           +  R+  TT IYVTHDQ EAMTLADRIV++SA          G IEQ+G P ELY  PAN
Sbjct: 179 LSERMSDTTMIYVTHDQVEAMTLADRIVVLSA----------GHIEQVGAPLELYERPAN 228

Query: 240 KFVAGFIGSPAMNFFEVTVEKERLVNQDGLSLALPQGQEKILE---EKGYLGKKVTLGIR 296
            FVA FIGSPAMN    T+       Q  +SLA   G+   L+        GK  + G+R
Sbjct: 229 LFVARFIGSPAMNVIPATITATG--QQTAVSLA--GGKSVTLDVPTNASENGKTASFGVR 284

Query: 297 PEDI---SSDQIVHETFPNASVTADILVSELLGSESMLYVK--FGSTEFTARVNARDSHS 351
           PED+    +D  + E          + + E LG  ++LY++    +    A++       
Sbjct: 285 PEDLRVTEADDFLFE--------GTVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVG 336

Query: 352 PGEKVQLTFNIAKGHFFD 369
            G+KV+ T + AK H FD
Sbjct: 337 RGDKVRFTADKAKLHLFD 354


Lambda     K      H
   0.318    0.135    0.379 

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: 357
Number of extensions: 14
Number of successful extensions: 5
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: 377
Length of database: 362
Length adjustment: 30
Effective length of query: 347
Effective length of database: 332
Effective search space:   115204
Effective search space used:   115204
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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