GapMind for catabolism of small carbon sources

 

Aligments for a candidate for scrK in Pseudomonas fluorescens FW300-N2E2

Align Fructokinase (EC 2.7.1.4) (characterized)
to candidate Pf6N2E2_804 Fructokinase (EC 2.7.1.4)

Query= reanno::pseudo3_N2E3:AO353_25910
         (314 letters)



>lcl|FitnessBrowser__pseudo6_N2E2:Pf6N2E2_804 Fructokinase (EC
           2.7.1.4)
          Length = 312

 Score =  524 bits (1350), Expect = e-153
 Identities = 259/311 (83%), Positives = 281/311 (90%)

Query: 1   MYLVCGEALFDFFSENAASSQASTVNYKAIAGGSPFNVAVGLRRLGVDSALFAGLSTDYL 60
           MYLVCGEALFDFFSE  A   AS VNYKAIAGGSPFNVAVGLRRLGV+SALF GLSTDYL
Sbjct: 1   MYLVCGEALFDFFSETEADGPASQVNYKAIAGGSPFNVAVGLRRLGVESALFTGLSTDYL 60

Query: 61  GRRLQQVLADEGVRADYLLDFDAPTTLAMVAVGANGSPHYSFRGEGCADRQLTLAHLPEL 120
           GRRL QVL +EGV A YL+DFDAPTTLAMVAVGANGSPHYSFRGEGCADRQL+LAHLP+L
Sbjct: 61  GRRLHQVLLNEGVSAQYLVDFDAPTTLAMVAVGANGSPHYSFRGEGCADRQLSLAHLPDL 120

Query: 121 SDEVRGLHIGSFSLVVQPIADTLLALVRRESGKRLISLDPNVRLNPEPDIELWRSRIAEL 180
             EVRGLH GSFSLVVQPIADTLLAL++RESG+RLISLDPNVRLNP+PDIELWRSRIA L
Sbjct: 121 GPEVRGLHFGSFSLVVQPIADTLLALMQRESGRRLISLDPNVRLNPQPDIELWRSRIATL 180

Query: 181 MKYADLIKVSDEDLSLLYPGREPQSVIDSWLEHRCQLVFLTRGGQGATVFSRRHGSWSAP 240
           ++YADLIKVSDEDL LLYP +EP+++I+ WL +RCQLVFLTRGGQGATVFSR+HGSWS P
Sbjct: 181 VQYADLIKVSDEDLDLLYPAKEPEAIIEGWLGNRCQLVFLTRGGQGATVFSRQHGSWSLP 240

Query: 241 ASKVVIADTVGAGDTFQAALITWLTEQQLDSVDGLQRLSREQIDAMLRFAISAAALTCSK 300
           +  V IADTVGAGDTFQAALI WLTEQQLDS++GL  L+REQI AML FAI AAALTC K
Sbjct: 241 SCPVKIADTVGAGDTFQAALIAWLTEQQLDSIEGLHTLTREQISAMLEFAIRAAALTCGK 300

Query: 301 TGPDLPYRHQL 311
           TGPDLPYRHQL
Sbjct: 301 TGPDLPYRHQL 311


Lambda     K      H
   0.320    0.136    0.398 

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: 398
Number of extensions: 10
Number of successful extensions: 1
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: 314
Length of database: 312
Length adjustment: 27
Effective length of query: 287
Effective length of database: 285
Effective search space:    81795
Effective search space used:    81795
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: 48 (23.1 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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