GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Sinorhizobium meliloti 1021

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate SM_b20661 SM_b20661 sugar uptake ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Smeli:SM_b20661
          Length = 355

 Score =  354 bits (908), Expect = e-102
 Identities = 188/347 (54%), Positives = 240/347 (69%), Gaps = 14/347 (4%)

Query: 19  PTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEGNLYIGDRRVNDVPPKDRD 78
           P +K  N++I+D EF + VGPSGCGK+T LRM+AGLE+IT G + IG++ VN +PPKDRD
Sbjct: 17  PVIKGVNIEIEDGEFVILVGPSGCGKSTLLRMLAGLENITAGEIRIGNQVVNRLPPKDRD 76

Query: 79  IAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAAKILDIAHLLDRKPKALSG 138
           IAMVFQNYALYPHMTV  NMAF L L   PK+EID+RV  AA+IL ++ LLDR P+ LSG
Sbjct: 77  IAMVFQNYALYPHMTVADNMAFSLMLAARPKSEIDKRVGVAAEILGLSKLLDRYPRQLSG 136

Query: 139 GQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRKLHQRLQTTVIYVTHDQTE 198
           GQRQRVA+GRAIVR+PQVFL DEPLSNLDAKLRV MRAEI++LHQRL+TT +YVTHDQ E
Sbjct: 137 GQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVAMRAEIKELHQRLKTTTVYVTHDQIE 196

Query: 199 AMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPAMNFIRGEIVQDGDAFYFR 258
           AMTM D+IVVM DG+++Q   P  +Y  P N+FVAGFIGSPAMN ++G +     + +  
Sbjct: 197 AMTMADKIVVMHDGIVEQIGAPLELYDNPANLFVAGFIGSPAMNMLKGRLDPADPSVFLT 256

Query: 259 APSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFMTTYPDSVLQMQVEVVEHM 318
           A   +  LP  R     A+ A G+ +V G+RPE       +M   P+  L  ++ V+E  
Sbjct: 257 ADGTA--LPVAR----PAAAAQGRDLVYGLRPE-------YMALDPNG-LPAEIAVIEPT 302

Query: 319 GSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIHIFDAET 365
           G E  L   +G + +      R     G ++ LAID   +H+FDA T
Sbjct: 303 GYETQLIARLGGHDVTCVFRERVNAKPGETIHLAIDAAHVHLFDAGT 349


Lambda     K      H
   0.321    0.138    0.395 

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: 409
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: 384
Length of database: 355
Length adjustment: 30
Effective length of query: 354
Effective length of database: 325
Effective search space:   115050
Effective search space used:   115050
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