GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Dechlorosoma suillum PS

Align ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized)
to candidate Dsui_0258 Dsui_0258 sulfate ABC transporter, ATP-binding protein

Query= BRENDA::P68187
         (371 letters)



>FitnessBrowser__PS:Dsui_0258
          Length = 360

 Score =  211 bits (536), Expect = 3e-59
 Identities = 128/341 (37%), Positives = 186/341 (54%), Gaps = 34/341 (9%)

Query: 3   SVQLQNVTKAWGEVVVSKDINLDIHEGEFVVFVGPSGCGKSTLLRMIAGLETITSGDLFI 62
           S++++N+ K +G  V   D++L I  GE V  +GPSGCGK+TLLR+IAG+ET   G +  
Sbjct: 2   SIEIRNIAKRFGNFVALDDVSLSIPTGELVALLGPSGCGKTTLLRIIAGMETADEGQVMF 61

Query: 63  GEKRMNDTPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEV----INQRVNQVA 118
                      ER VG VFQ YAL+ H++V EN++FGL++   K+      I +RV  + 
Sbjct: 62  EGSEATHLHARERQVGFVFQHYALFRHMNVFENVAFGLRVKPRKERPCESEIRKRVMDLL 121

Query: 119 EVLQLAHLLDRKPKALSGGQRQRVAIGRTLVAEPSVFLLDEPLSNLDAALRVQMRIEISR 178
            ++QL  L DR P  LSGGQRQR+A+ R L  EP V LLDEP   LD  +R ++R  + R
Sbjct: 122 SLVQLDWLADRYPTQLSGGQRQRIALARALAVEPKVLLLDEPFGALDTKVRKELRRWLRR 181

Query: 179 LHKRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPK 238
           LH  +  + ++VTHDQ EA+ +AD++VV++ GR+ QVG P E+Y  PA  FV  F+G+  
Sbjct: 182 LHDEMHISSVFVTHDQEEALEVADRVVVMNKGRIEQVGSPDEVYSNPASPFVYQFLGN-- 239

Query: 239 MNFLPVKVTATAIDQVQVELPMPNRQQVWLPVESRDVQVGANMSLGIRPEHLLPSDIA-D 297
           +N    +V                    W  V   DV  G      IRP  +    +A  
Sbjct: 240 VNVFHSRV-----------------HGAWAEVARDDVPAGQEAVAFIRPHDIDIDTVATP 282

Query: 298 VILEGEVQVVEQLGNETQIHIQIPSIRQNLVYRQNDVVLVE 338
             LE +V  V+ +G         P +R  +++ Q ++V VE
Sbjct: 283 ESLEAKVSYVQTIG---------PLVRVEVIH-QGELVEVE 313


Lambda     K      H
   0.320    0.137    0.393 

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: 317
Number of extensions: 11
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: 371
Length of database: 360
Length adjustment: 30
Effective length of query: 341
Effective length of database: 330
Effective search space:   112530
Effective search space used:   112530
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