GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Pseudomonas fluorescens FW300-N2E3

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate AO353_07265 AO353_07265 spermidine/putrescine ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_07265
          Length = 374

 Score =  207 bits (526), Expect = 5e-58
 Identities = 116/325 (35%), Positives = 186/325 (57%), Gaps = 20/325 (6%)

Query: 2   VRIIVKNVSKVFKKGKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTGE 61
           V +  + V K +  G+ + + ++N+ I  GE   +LGPSG+GKTT + ++AG + P+ GE
Sbjct: 13  VLVSFRGVQKSYD-GENLIVKDLNLEIRKGEFLTLLGPSGSGKTTSLMMLAGFETPTAGE 71

Query: 62  LYFDDRLVASNGKLIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKRV 121
           +    R + +     VPP  R IGMVFQ +AL+P++T  EN+AFPLT   ++K ++  RV
Sbjct: 72  ILLAGRAINN-----VPPHKRDIGMVFQNYALFPHMTVAENLAFPLTVRGLNKSDVSDRV 126

Query: 122 EEVAKILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSARA 181
           + V  ++ +      +P +LSGGQQQRVALARALV +P L+L+DEP   LD ++R+  + 
Sbjct: 127 KRVLSMVQLDAFAQRYPAQLSGGQQQRVALARALVFEPQLVLMDEPLGALDKQLREHMQM 186

Query: 182 LVKEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASLI 241
            +K +  RLGVT++ V+HD  +   ++DRV V  +G++ Q+  P +LY+ P +  VA+ I
Sbjct: 187 EIKHLHQRLGVTVVYVTHDQGEALTMSDRVAVFHQGEIQQIAPPRELYEKPKNTFVANFI 246

Query: 242 GEINELEGKV-----------TNEGVVIGSLRFPVSVSSDRAIIGIRPEDVKLSKDVIKD 290
           GE N L G++              G  + +L   V  + +   + IRPE V L+      
Sbjct: 247 GENNRLNGRLHSHTGDRCVVELGRGEKVEALAVNVGKTGEPVTLSIRPERVSLNG---SS 303

Query: 291 DSWILVGKGKVKVIGYQGGLFRITI 315
           +S +    G+V    Y G   R+ +
Sbjct: 304 ESCVNRFSGRVAEFIYLGDHVRVRL 328


Lambda     K      H
   0.319    0.139    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: 323
Number of extensions: 13
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: 353
Length of database: 374
Length adjustment: 29
Effective length of query: 324
Effective length of database: 345
Effective search space:   111780
Effective search space used:   111780
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 (21.7 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