GapMind for catabolism of small carbon sources

 

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

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate AO353_25130 AO353_25130 ABC transporter

Query= reanno::psRCH2:GFF857
         (371 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_25130
          Length = 381

 Score =  372 bits (956), Expect = e-108
 Identities = 206/362 (56%), Positives = 249/362 (68%), Gaps = 3/362 (0%)

Query: 1   MASVTLRDICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDL 60
           M  + L ++ K   G  I R + L+I  GEFVVFVGPSGCGKSTLLRLIAGL+ I +GDL
Sbjct: 1   MIKLKLDNVNKQLGGVRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICAGDL 60

Query: 61  LIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEI 120
           LID +RVNDL P++R VGMVFQSYALYPHM+V +N++FGLKLA  +K  ++ RV   A+I
Sbjct: 61  LIDERRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTEKSSLRERVLRTAQI 120

Query: 121 LQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLH 180
           LQLDKLL+RKPK+LSGGQRQRVA+GR M REP + LFDEPLSNLDA LRVQMR EIARLH
Sbjct: 121 LQLDKLLQRKPKELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLH 180

Query: 181 QRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQMN 240
            R+ STMIYVTHDQVEAMTLADKIVVLN G + QVG P  LY  P +RFVAGFLGSP+MN
Sbjct: 181 ARLGSTMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMN 240

Query: 241 FVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFVMPDEADFTFHG 300
           F+  R + A  ET  ++ P     +LP D S ++   PL+LG+RPEH V    AD T   
Sbjct: 241 FLAAR-LHAPGETSLVDTPVLGMTSLPFDSSNLAADTPLSLGVRPEH-VSLKAADGTVGV 298

Query: 301 QITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADKCHLFRENGEAC 360
            +T  E LG    ++L   +   +I  C + N     G+     L     HLF  +G A 
Sbjct: 299 IVTGVEYLGSETYVHLDTGQDDPLICRC-EVNAGWQVGDRVELQLDIGNLHLFDADGTAL 357

Query: 361 TR 362
            R
Sbjct: 358 RR 359


Lambda     K      H
   0.322    0.139    0.405 

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: 421
Number of extensions: 14
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: 371
Length of database: 381
Length adjustment: 30
Effective length of query: 341
Effective length of database: 351
Effective search space:   119691
Effective search space used:   119691
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 (21.9 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