GapMind for catabolism of small carbon sources

 

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

Align Extracellular sucrase; Beta-fructofuranosidase; Invertase; Protein B46; Saccharase; EC 3.2.1.26 (characterized)
to candidate AO353_04255 AO353_04255 sucrase

Query= SwissProt::F8DT27
         (413 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_04255
          Length = 426

 Score =  372 bits (955), Expect = e-107
 Identities = 189/411 (45%), Positives = 258/411 (62%), Gaps = 27/411 (6%)

Query: 7   SRWTRAQAMKVNKFDLTTSMPEIGTDFPIMRDDLWLWDTWPLRDINGNPVSFKGWNVIFS 66
           S WTRA A+KV+  D TT+ P +  DFP++ +++++WDT PLRDI+GN  S  GW+VIF+
Sbjct: 16  SLWTRADALKVHADDPTTTQPLVSADFPVLSNEVFIWDTMPLRDIDGNVASVDGWSVIFT 75

Query: 67  LVADR--NIP--------------WNDRHSHARIGYFYSKDGKSWVYGGHLLQESANTRT 110
           L ADR  N P              WNDRH  A++ Y++S+ GK W +GG ++ +  +  T
Sbjct: 76  LTADRHPNDPEYIDENGNYDIIRDWNDRHGRAKMYYWFSRTGKDWQFGGRVMAQGVSPTT 135

Query: 111 AEWSGGTIMAPGSRNQVETFFTSTLFDKNGVREAVAAVTKGRIYADSEGVWFKGFDQSTD 170
            EW+G  I+    +  V+ ++T+          A     +GR+     GV   GF + T 
Sbjct: 136 REWAGSPILL-NDQGDVDLYYTAV------TPGATIVKVRGRVVTTEHGVEMVGFKKVTS 188

Query: 171 LFQADGLFYQNYAENNLWNFRDPHVFINPEDGETYALFEANVATVRGEDDIGEDEIGPVP 230
           LF+ADG  YQ   +N  W FRDP  F +P+DG+ Y LFE NVA  RG   +GE EIG VP
Sbjct: 189 LFEADGEIYQTETQNPYWGFRDPWPFRDPKDGKLYMLFEGNVAGERGSHKVGEAEIGDVP 248

Query: 231 ANTVVPKDANLCSASIGIARCLSPDRTEWELLPPLLTAFGVNDQMERPHVIFQNGLTYLF 290
                  ++   +A +GIA     D  +WE+LPPLLTA GVNDQ ERPH +FQ+G  YLF
Sbjct: 249 PGYEDVGNSRFQTACVGIAVANDEDGDDWEMLPPLLTAVGVNDQTERPHFLFQDGKYYLF 308

Query: 291 TISHDSTYADGLTGSDGLYGFVSENGIFGPYEPLNGSGLVLGGPASQPTEAYAHYIMNNG 350
           TISH  TYADG+TG DG+YGFV+++ +FGPY PLNGSGLVLG P+SQP + Y+HY+M NG
Sbjct: 309 TISHKFTYADGVTGPDGVYGFVADS-LFGPYVPLNGSGLVLGNPSSQPFQTYSHYVMPNG 367

Query: 351 LVESFINEIIDPKSG---KVIAGGSLAPTVRVELQGHETFATEVFDYGYIP 398
           LV SFI+ +   +S    +   GG+ APTV ++++G +TF    +DYGYIP
Sbjct: 368 LVTSFIDTVPTKESDTGMQYRVGGTEAPTVGIKVKGQQTFVVAEYDYGYIP 418


Lambda     K      H
   0.319    0.137    0.438 

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: 658
Number of extensions: 41
Number of successful extensions: 5
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: 413
Length of database: 426
Length adjustment: 32
Effective length of query: 381
Effective length of database: 394
Effective search space:   150114
Effective search space used:   150114
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: 50 (23.9 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