GapMind for catabolism of small carbon sources

 

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

Align Extracellular sucrase; Beta-fructofuranosidase; Invertase; Protein B46; Saccharase; EC 3.2.1.26 (characterized)
to candidate AO356_15155 AO356_15155 sucrase

Query= SwissProt::F8DT27
         (413 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_15155
          Length = 424

 Score =  377 bits (968), Expect = e-109
 Identities = 189/409 (46%), Positives = 259/409 (63%), Gaps = 25/409 (6%)

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

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

Query: 111 AEWSGGTIMAPGSRNQVETFFTSTLFDKNGVREAVAAVTKGRIYADSEGVWFKGFDQSTD 170
            EW+G  I+    R +V+ ++T+          A     +GR+     GV   GF++   
Sbjct: 136 REWAGTPILL-NDRGEVDLYYTAV------TPGATIVKVRGRVVTTEHGVSMVGFEKVKP 188

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

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

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

Query: 351 LVESFINEIIDPKSG-KVIAGGSLAPTVRVELQGHETFATEVFDYGYIP 398
           LV SFI+ +   ++G ++  GG+ APTV ++++G +TF    +DYGYIP
Sbjct: 368 LVTSFIDSVPTDETGTQIRVGGTEAPTVGMKIKGQQTFVVAEYDYGYIP 416


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: 652
Number of extensions: 50
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: 424
Length adjustment: 32
Effective length of query: 381
Effective length of database: 392
Effective search space:   149352
Effective search space used:   149352
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