GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Caulobacter crescentus NA1000

Align Spermidine/putrescine ABC transporter, spermidine/putrescine-binding protein, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate CCNA_03239 CCNA_03239 spermidine/putrescine-binding protein

Query= TCDB::Q97Q45
         (356 letters)



>FitnessBrowser__Caulo:CCNA_03239
          Length = 368

 Score =  198 bits (504), Expect = 2e-55
 Identities = 102/300 (34%), Positives = 164/300 (54%), Gaps = 1/300 (0%)

Query: 33  DSQKLVIYNWGDYIDPELLTQFTEETGIQVQYETFDSNEAMYTKIKQGGTTYDIAIPSEY 92
           +  KL  YNW  YI    L  F + TGI V    F +N+ ++ K+K G   +D+ +PS  
Sbjct: 46  EEAKLNFYNWDTYIGETTLGDFKKATGIDVNMSLFATNDELFAKLKAGNPGFDVVVPSNE 105

Query: 93  MINKMKDEDLLVPLDYSKIEGIENIGPEFLNQSFDPGNKFSIPYFWGTLGIVYNETMVDE 152
            + +M    LL PLD++KI  ++NI P FLN  FDPG KFS+PY W  LGI Y ++ V  
Sbjct: 106 FVTRMSQGGLLEPLDHAKIPNMKNIDPSFLNPEFDPGRKFSMPYTWLLLGIGYRKSKVKG 165

Query: 153 APEHWDDLW-KPEYKNSIMLFDGAREVLGLGLNSLGYSLNSKDLQQLEETVDKLYKLTPN 211
            P+ W  L+   +YK  I L   + +++ L    LG+S+N+     L +    L K  P 
Sbjct: 166 VPDSWKWLFDSDQYKGRIALLSESADLVRLSAKYLGHSVNNIPQDMLPKIEQMLIKQKPF 225

Query: 212 IKAIVADEMKGYMIQNNVAIGVTFSGEASQMLEKNENLRYVVPTEASNLWFDNMVIPKTV 271
           +KA   D  +  ++   V + + ++G+ +Q ++++ +L +VVP E S +  D + IPK  
Sbjct: 226 VKAFHDDNGQDMLMSGEVDLVLEYNGDIAQAMKEDPDLDFVVPKEGSLINSDTLCIPKGA 285

Query: 272 KNQNSAYAFINFMLKPENALQNAEYVGYSTPNLPAKELLPEETKEDKAFYPDVETMKHLE 331
              N+A+AFIN++L  +   + ++ + Y TPN  AK L+PE+ K +   +P  + M   E
Sbjct: 286 PRPNNAHAFINYLLDAQAGAEISKTILYPTPNAAAKALMPEDYKNNPVIFPPADVMAKCE 345


Lambda     K      H
   0.316    0.135    0.397 

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: 320
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: 356
Length of database: 368
Length adjustment: 29
Effective length of query: 327
Effective length of database: 339
Effective search space:   110853
Effective search space used:   110853
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 (21.6 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