GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas fluorescens FW300-N2C3

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate AO356_05180 AO356_05180 sugar ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_05180
          Length = 386

 Score =  196 bits (497), Expect = 1e-54
 Identities = 114/327 (34%), Positives = 186/327 (56%), Gaps = 13/327 (3%)

Query: 27  LKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRASPQERNIAQVF 86
           +++  +DG    L+GPSGCGK+T++N ++GL   + G ++   +DV+  SP++R+IA VF
Sbjct: 24  IELSIKDGEFLILVGPSGCGKSTLMNCIAGLETITGGAIMIGDQDVSGMSPKDRDIAMVF 83

Query: 87  QFPVIYDTMTVAENLAFPLRNRKVPEGQIKQRVGVIAEMLEMSGQLNQRAAGLAADAKQK 146
           Q   +Y TM+V EN+ F L+ RK+ +  I + V  +A++L++   LN++   L+   +Q+
Sbjct: 84  QSYALYPTMSVRENIEFGLKIRKMNQSAIDEEVNRVAKLLQIEHLLNRKPGQLSGGQQQR 143

Query: 147 ISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHELKLTLIYVTHDQVEALTF 206
           +++GR L R      LFDEPL+ +D  L+ ++R ++K +H  LK T +YVTHDQ+EA+T 
Sbjct: 144 VAMGRALARRP-KIYLFDEPLSNLDAKLRVEMRTEMKLMHQRLKTTTVYVTHDQIEAMTL 202

Query: 207 ADQVVVMTRGKAVQVGSADALFERPAHTFVGHFIGSPGMNFLP---AHRDGENLSVAGH- 262
            D+V VM  G   Q G+   ++  PA+ FV  FIGSP MNF+P     +DG  L++    
Sbjct: 203 GDKVAVMKDGIIQQFGTPKDIYTNPANLFVASFIGSPPMNFIPLRLQRKDGRLLALLDSG 262

Query: 263 --RLASPVG---RALPAGALQVGIRPEYLALA--QPQQAGALPGTVVQVQDIGTYQMLTA 315
             R   P+G     L    + +G+RPE + LA  +P     +   V   +  G   ++  
Sbjct: 263 QARCELPMGMQDAGLEDREVILGMRPEQIMLAGSEPNGLPTIRAEVQVTEPTGPDTLVFV 322

Query: 316 KVGEHTVKARFTPETRLPSSGDTAWLQ 342
            + +  V  R  P+   P  G+T  LQ
Sbjct: 323 SLNDTKVCCRLAPDV-APQVGETLTLQ 348


Lambda     K      H
   0.320    0.136    0.395 

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: 329
Number of extensions: 18
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: 358
Length of database: 386
Length adjustment: 30
Effective length of query: 328
Effective length of database: 356
Effective search space:   116768
Effective search space used:   116768
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