Aligments for a candidate for BPHYT_RS16930 in Pseudomonas fluorescens FW300-N2E2

GapMind for catabolism of small carbon sources

Aligments for a candidate for BPHYT_RS16930 in Pseudomonas fluorescens FW300-N2E2

Align Arabinose import ATP-binding protein AraG; EC 7.5.2.12 (characterized, see rationale)
to candidate Pf6N2E2_1456 D-xylose transport ATP-binding protein XylG

Query= uniprot:B2SYR5
         (512 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1456
          Length = 518

 Score =  348 bits (894), Expect = e-100
 Identities = 208/508 (40%), Positives = 321/508 (63%), Gaps = 27/508 (5%)

Query: 5   LRFDNIGKVFPGVRALDGVSFDVNVGQVHGLMGENGAGKSTLLKILGGEYQPDS--GRVM 62
           L+ + I K F GV+AL+G+   V  G+  GL GENGAGKSTL+K+L   Y   +  G ++
Sbjct: 6   LQMNGIVKTFGGVKALNGIDIKVRPGECVGLCGENGAGKSTLMKVLSAVYPYGTWDGEIL 65

Query: 63  IDGNEVRFTSAASSIAAGIAVIHQELQYVPDLTVAENLLLGQ---LP----NSLGWVNKR 115
            DG  ++  S + + AAGI +IHQEL  VPDL+VAEN+ +G    LP    N    +++ 
Sbjct: 66  WDGQPLKAQSISETEAAGIVIIHQELTLVPDLSVAENIFMGHELTLPGGRMNYPAMIHRA 125

Query: 116 EAKRFVRE-RLEAMGVALDPNAKLRKLSIAQRQMVEICKALLRNARVIALDEPTSSLSHR 174
           EA   +RE ++  M V+L     + +     +Q+VEI KAL + AR++ LDEP+S+L+  
Sbjct: 126 EA--LMRELKVPDMNVSLP----VSQYGGGYQQLVEIAKALNKQARLLILDEPSSALTRS 179

Query: 175 ETEVLFKLVRDLRADNRAMIYISHRMDEIYELCDACTIFRDGRKIASHPTLEGVTRDTIV 234
           E EVL  ++RDL+A   A +YISH++DE+  +CD  ++ RDG+ IA+   +  ++   I+
Sbjct: 180 EIEVLLDIIRDLKAKGVACVYISHKLDEVAAVCDTISVIRDGKHIAT-TAMADMSIPKII 238

Query: 235 SEMVGREISDIYNYSARPLGEVRFAAKGIEGHALAQPA-------SFEVRRGEIVGFFGL 287
           ++MVGRE+S++Y      +GEV F A+    + +  P        SF ++RGEI+G  GL
Sbjct: 239 TQMVGREMSNLYPTEPHDVGEVIFEARHFTCYDVDNPRRKRVDDISFVLKRGEILGIAGL 298

Query: 288 VGAGRSELMHLVYGA-DHKKGGELLLDGKPIKVRSAGEAIRHGIVLCPEDRKEEGIVAMA 346
           VGAGR+EL+  ++GA   +  GE+ L+G+ I  R+  ++IR G+ + PEDRK +GI+   
Sbjct: 299 VGAGRTELVSALFGAYPGRYEGEVWLNGQQIDTRTPLKSIRAGLCMVPEDRKRQGIIPDL 358

Query: 347 TVSENINISCRRHYLRVGMFLDRKKEAETADRFIKLLKIKTPSRRQKIRFLSGGNQQKAI 406
            V +NI ++   +Y ++   +D + E  + D+ I  + +KT S    I  LSGGNQQKA+
Sbjct: 359 GVGQNITLAVLDNYSKLTR-IDAEAELGSIDKEISRMHLKTASPFLPITSLSGGNQQKAV 417

Query: 407 LSRWLAEPDLKVVILDEPTRGIDVGAKHEIYNVIYQLAERGCAIVMISSELPEVLGVSDR 466
           L++ L     +V+ILDEPTRG+DVGAK+EIY ++  LA  G +I+M+SSEL EVLGVSDR
Sbjct: 418 LAKMLLTKP-RVLILDEPTRGVDVGAKYEIYKLMGALAAEGVSIIMVSSELAEVLGVSDR 476

Query: 467 IVVMRQGRISGELTRKDATEQSVLSLAL 494
           ++V+  G++ G+    + T++ VL+ AL
Sbjct: 477 VLVIGDGQLRGDFINHELTQEQVLAAAL 504


Lambda     K      H
   0.320    0.136    0.385 

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: 666
Number of extensions: 37
Number of successful extensions: 12
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: 512
Length of database: 518
Length adjustment: 35
Effective length of query: 477
Effective length of database: 483
Effective search space:   230391
Effective search space used:   230391
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: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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

GapMind for catabolism of small carbon sources