Aligments for a candidate for rhaT' in Pseudomonas fluorescens FW300-N1B4

GapMind for catabolism of small carbon sources

Aligments for a candidate for rhaT' in Pseudomonas fluorescens FW300-N1B4

Align RhaT, component of Rhamnose porter (Richardson et al., 2004) (Transport activity is dependent on rhamnokinase (RhaK; AAQ92412) activity (Richardson and Oresnik, 2007) This could be an example of group translocation!) (characterized)
to candidate Pf1N1B4_6034 Ribose ABC transport system, ATP-binding protein RbsA (TC 3.A.1.2.1)

Query= TCDB::Q7BSH4
         (512 letters)



>lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_6034 Ribose ABC transport
           system, ATP-binding protein RbsA (TC 3.A.1.2.1)
          Length = 517

 Score =  287 bits (735), Expect = 6e-82
 Identities = 174/496 (35%), Positives = 276/496 (55%), Gaps = 12/496 (2%)

Query: 19  AILEMRGISQIFPGVKALDNVSIALHPGTVTALIGENGAGKSTLVKILTGIYRPNEGEIL 78
           A+L + GI + +     L  + + L  G V AL GENGAGKSTL KI+ G+  P  G++ 
Sbjct: 8   AVLSVSGIGKTY-AQPVLTGIDLTLMRGEVLALTGENGAGKSTLSKIIGGLVAPTTGQMR 66

Query: 79  VDGRPTTFASAQAAIDAGVTAIHQETVLFDELTVAENIFLGHAPRTRFRTIDWQTMNSRS 138
             GR     S   A + G+  + QE  L   L+VAEN+FL + P        W +     
Sbjct: 67  FQGRDYRPGSRSQAEELGIRMVMQELNLLPTLSVAENLFLDNLPSHG----GWISRKQLR 122

Query: 139 KALLTALES----NIDPTIRLKDLSIAQRHLVAIARALSIEARIVIMDEPTAALSRKEID 194
           KA + A+       IDP   + +L I  + +V IAR L  +  ++I+DEPTA L+ +E++
Sbjct: 123 KAAIEAMAQVGLDAIDPDTLVGELGIGHQQMVEIARNLIGDCHVLILDEPTAMLTAREVE 182

Query: 195 DLFRIVRGLKEQGKAILFISHKFDELYEIADDFVVFPRRSRRPVRGVSRKTPQDEIVRMM 254
            LF  +  L+ +G +I++ISH+ +EL  +A    V    +   V  ++     +++V +M
Sbjct: 183 MLFEQITRLQARGVSIIYISHRLEELARVAQRIAVLRDGNLVCVEPMANYN-SEQLVTLM 241

Query: 255 VGRDVENVFPKIDVAIGGPVLEIRNYSHRTEFRDISFTLRKGEILGVYGLIGAGRSELSQ 314
           VGR++          IG P L ++  +   + RD+SF +R GEI G+ GLIGAGR+EL +
Sbjct: 242 VGRELGEHIDMGPRKIGAPALTVKGLTRSDKVRDVSFEVRAGEIFGISGLIGAGRTELLR 301

Query: 315 SLFGITKPLSGKMVL--EGQEITIHSPQDAIRAGIVYVPEERGRHGLALPMPIFQNMTLP 372
            +FG     SG + L    Q ++I SP DA+  GI  + E+R   GL L   I  N+ L 
Sbjct: 302 LIFGADTADSGTVALGASAQVVSIRSPADAVGHGIALITEDRKGEGLLLTQSISANIALG 361

Query: 373 SLARTSRRGFLRAANEFALARKYAERLDLRAAALSVPVGTLSGGNQQKVVIGKWLATAPK 432
           ++   S  GF+   +E +LA++    + +R+++ +  V  LSGGNQQKVVIG+WL     
Sbjct: 362 NMPVISSGGFVNNGDEMSLAQRQINAMRIRSSSPTQLVSELSGGNQQKVVIGRWLERDCT 421

Query: 433 VIILDEPTKGIDIGSKAAVHGFISELAAEGLSIIMVSSELPEIIGMSDRVLVMKEGLSAG 492
           V++ DEPT+GID+G+K  ++  + EL  +G ++++VSS+L E++ + DR+ V+  G    
Sbjct: 422 VMLFDEPTRGIDVGAKFDIYALLGELTRQGKALVVVSSDLRELMLICDRIGVLSAGRLID 481

Query: 493 IFERAELSPEALVRAA 508
            FER   + + L+ AA
Sbjct: 482 TFERDSWTQDDLLAAA 497



 Score = 84.3 bits (207), Expect = 9e-21
 Identities = 67/222 (30%), Positives = 107/222 (48%), Gaps = 5/222 (2%)

Query: 289 ISFTLRKGEILGVYGLIGAGRSELSQSLFGITKPLSGKMVLEGQEITIHSPQDAIRAGIV 348
           I  TL +GE+L + G  GAG+S LS+ + G+  P +G+M  +G++    S   A   GI 
Sbjct: 27  IDLTLMRGEVLALTGENGAGKSTLSKIIGGLVAPTTGQMRFQGRDYRPGSRSQAEELGIR 86

Query: 349 YVPEERGRHGLALPMPIFQNMTLPSLARTSRRGFLRAANEFALARKYAERLDLRAAALSV 408
            V +E     L   + + +N+ L +L   S  G++        A +   ++ L A     
Sbjct: 87  MVMQELN---LLPTLSVAENLFLDNLP--SHGGWISRKQLRKAAIEAMAQVGLDAIDPDT 141

Query: 409 PVGTLSGGNQQKVVIGKWLATAPKVIILDEPTKGIDIGSKAAVHGFISELAAEGLSIIMV 468
            VG L  G+QQ V I + L     V+ILDEPT  +       +   I+ L A G+SII +
Sbjct: 142 LVGELGIGHQQMVEIARNLIGDCHVLILDEPTAMLTAREVEMLFEQITRLQARGVSIIYI 201

Query: 469 SSELPEIIGMSDRVLVMKEGLSAGIFERAELSPEALVRAATG 510
           S  L E+  ++ R+ V+++G    +   A  + E LV    G
Sbjct: 202 SHRLEELARVAQRIAVLRDGNLVCVEPMANYNSEQLVTLMVG 243


Lambda     K      H
   0.320    0.137    0.382 

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: 629
Number of extensions: 34
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 512
Length of database: 517
Length adjustment: 35
Effective length of query: 477
Effective length of database: 482
Effective search space:   229914
Effective search space used:   229914
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)
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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