GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Thauera aminoaromatica S2

Align Putrescine-binding periplasmic protein SpuD (characterized)
to candidate WP_004307355.1 C665_RS09750 polyamine ABC transporter substrate-binding protein

Query= SwissProt::Q02UB7
         (367 letters)



>NCBI__GCF_000310185.1:WP_004307355.1
          Length = 362

 Score =  270 bits (691), Expect = 3e-77
 Identities = 144/367 (39%), Positives = 223/367 (60%), Gaps = 5/367 (1%)

Query: 1   MMKRFGKTLLALTLAGSVAGMAQAADNKVLHVYNWSDYIAPDTLEKFTKETGIKVVYDVY 60
           M  +FG  +  L LA   AG A AA+  +L+VYNW+DYIA DT+  F K +GI+V YD+Y
Sbjct: 1   MTLKFG-WMAVLALA---AGAAVAAEEPILNVYNWNDYIAADTIPAFEKASGIEVRYDLY 56

Query: 61  DSNEVLEAKLLAGKSGYDVVVPSNSFLAKQIKAGVYQKLDKSKLPNWKNLNKDLMHTLEV 120
           DSN  L+ KLL G SGYDVV PS  +  KQI+AG++Q LDKS+LPN  +++  ++  + V
Sbjct: 57  DSNATLQGKLLTGGSGYDVVYPSVEYAGKQIQAGIFQPLDKSRLPNLVHIDPLILEAVAV 116

Query: 121 SDPGNEHAIPYMWGTIGIGYNPDKVKAAFGDNAPVDSWDLVFKPENIQKLKQCGVSFLDS 180
           +DPGN + +PYMW TIG+  N DKV  A     P ++WDL+F P    +LK CG++ +D 
Sbjct: 117 ADPGNRYLVPYMWFTIGVAINVDKVMKALDGKLPDNAWDLLFDPALTARLKGCGIALMDE 176

Query: 181 PTEILPAALHYLGYKPDTDNPKELKAAEELFLKIRPYVTYFHSSKYISDLANGNICVAIG 240
            ++++PAA+   G  P   +P +++AA E    +R  +  F+++  I  +A G++CVA+ 
Sbjct: 177 ASDVIPAAMLDAGLDPVKMDPADIRAAVEHIRPVRKDIRSFNTAP-IEQMAKGSLCVAMM 235

Query: 241 YSGDIYQAKSRAEEAKNKVTVKYNIPKEGAGSFFDMVAIPKDAENTEGALAFVNFLMKPE 300
           +SGD   A  RA+   ++V ++Y IP  GA    D++AIP+DA +   A  +++ +M P 
Sbjct: 236 FSGDARIAARRAQIGGSEVRLQYLIPAVGAMMSVDVMAIPRDAPHPHNAHRWIDAMMDPA 295

Query: 301 IMAEITDVVQFPNGNAAATPLVSEAIRNDPGIYPSEEVMKKLYTFPDLPAKTQRAMTRSW 360
            +A I++   + + N AA  L    +R+DP I   E V + L   P L    QR +T++ 
Sbjct: 296 TVARISNETFYISANTAALALTDATLRDDPAINVPEAVKRTLRAKPVLGKDVQRELTQAL 355

Query: 361 TKIKSGK 367
            + K+ +
Sbjct: 356 NRFKAAR 362


Lambda     K      H
   0.315    0.133    0.390 

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: 341
Number of extensions: 17
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: 367
Length of database: 362
Length adjustment: 29
Effective length of query: 338
Effective length of database: 333
Effective search space:   112554
Effective search space used:   112554
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: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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