GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Shewanella oneidensis MR-1

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate 200449 SO1271 polyamine ABC transporter, ATP-binding protein (NCBI ptt file)

Query= reanno::psRCH2:GFF857
         (371 letters)



>FitnessBrowser__MR1:200449
          Length = 378

 Score =  228 bits (580), Expect = 3e-64
 Identities = 125/325 (38%), Positives = 193/325 (59%), Gaps = 15/325 (4%)

Query: 9   ICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDLLIDNQRVN 68
           + K +D       + L I  GE    +G SG GKSTLLR++AG E  TSG + +D + + 
Sbjct: 26  VSKLFDDVRAVDDVSLTINKGEIFALLGGSGSGKSTLLRMLAGFERPTSGRIYLDGEDIT 85

Query: 69  DLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEILQLDKLLE 128
           DLPP +R + M+FQSYAL+PHMTVA+N+AFGLK   + K EI++RV+ + +++ +++  +
Sbjct: 86  DLPPYERPINMMFQSYALFPHMTVAQNIAFGLKQDKLPKAEIEQRVQEMLKLVHMEQYGK 145

Query: 129 RKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLHQRIRSTMI 188
           RKP  LSGGQRQRVA+ R++ + PK+ L DEP+  LD  LR QM++E+  + +R+  T +
Sbjct: 146 RKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRTQMQLEVVEILERVGVTCV 205

Query: 189 YVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLG-----SPQMNFVE 243
            VTHDQ EAMT+A +I +++ G IAQ G P+ +Y  P +R +A F+G     S ++   E
Sbjct: 206 MVTHDQEEAMTMAGRISIMSDGWIAQTGSPMDIYESPNSRMIAEFIGSVNLFSGEIEVDE 265

Query: 244 VRAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFVM---PDEADFTF-H 299
           V  +   P  +      GY +T  ++   V       L +RPE  ++     E ++ +  
Sbjct: 266 VDHLIIKPNDLARSFYVGYGVTTSLEDKRV------WLAVRPEKTIISREQPEGEYNWAK 319

Query: 300 GQITVAERLGQYNLLYLTLERLQDV 324
           G +     LG  ++ Y+ LE  Q V
Sbjct: 320 GIVHDIAYLGGISVYYIRLENGQIV 344


Lambda     K      H
   0.322    0.139    0.405 

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: 323
Number of extensions: 17
Number of successful extensions: 1
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: 378
Length adjustment: 30
Effective length of query: 341
Effective length of database: 348
Effective search space:   118668
Effective search space used:   118668
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 (21.9 bits)
S2: 50 (23.9 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