GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Desulfovibrio vulgaris Miyazaki F

Align Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate 8500851 DvMF_1589 ABC transporter related (RefSeq)

Query= TCDB::Q97Q42
         (385 letters)



>FitnessBrowser__Miya:8500851
          Length = 354

 Score =  214 bits (544), Expect = 4e-60
 Identities = 136/353 (38%), Positives = 199/353 (56%), Gaps = 33/353 (9%)

Query: 6   IEFKNVSKVFEDSNTKVLKDINFELEEGKFYTLLGASGSGKSTILNIIAGLLDATTGDI- 64
           +   NV+K F       +  +N E+  G+ +++LG SG GK+T L ++AG  D   G+I 
Sbjct: 4   VRLVNVTKRF--GGVTAVDSLNLEIGRGECFSMLGPSGCGKTTTLRMVAGFEDLDDGEIH 61

Query: 65  ----MLDGVRIND-IPTNKRDVHTVFQSYALFPHMNVFENVAFPLRLRKIDKKEIEQRVA 119
               +L   R N  +P  KRD   VFQ++A++PH++V+ENVAFPLR+R++   EI++R  
Sbjct: 62  VGDRLLSARRNNYYLPPEKRDFGMVFQAFAVWPHLSVYENVAFPLRIRRLSAAEIDRRTR 121

Query: 120 EVLKMVQLEGYEKRSIRKLSGGQRQRVAIARAIINQPRVVLLDEPLSALDLKLRTDMQYE 179
           E L    L    ++S   LSGG +QRVA+ARA+   P V+LLDEPLS+LD  LR +M++E
Sbjct: 122 EALHHTSLADVAQKSPDDLSGGGKQRVALARALAINPDVMLLDEPLSSLDPHLREEMRFE 181

Query: 180 LRELQQRLGITFVFVTHDQEEALAMSDWIFVMNDGEIVQSGTPVDIYDEPINHFVATFIG 239
           +++LQ+  G + ++VTHDQ EA+A+SD I VM +G + Q GTP+D+Y  P N FV  FIG
Sbjct: 182 IKDLQRTFGFSILYVTHDQSEAMALSDRIMVMRNGVVQQVGTPLDVYTNPANSFVFGFIG 241

Query: 240 ESNILPGTMIEDYLVEFNGKRFEAVDGGMKPNEP----------VEVVIRPEDLRITLPE 289
            SN L   +  + LV  NG      D  + P  P            +  RP ++  T   
Sbjct: 242 LSNFLDVNLTPEGLVRVNGG-----DARVTPATPPSARLVSAGRAALASRPSEIDFT--A 294

Query: 290 EGKLQVKVDTQLFRGVHYEIIAY--DELGNEWMIHSTRKA---IVGEEIGLDF 337
           EG L+  V  + + G   EI+ Y  D  G E  +   R+A     G+  GL F
Sbjct: 295 EGGLRGVVRRRAYLG---EIVDYRIDVSGQEVRVQKGRRAPGPAEGDACGLVF 344


Lambda     K      H
   0.318    0.138    0.386 

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: 291
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: 385
Length of database: 354
Length adjustment: 30
Effective length of query: 355
Effective length of database: 324
Effective search space:   115020
Effective search space used:   115020
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