Alignments for a candidate for fruK in Pseudomonas stutzeri RCH2

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruK in Pseudomonas stutzeri RCH2

Align Fructose import ATP-binding protein FruK; EC 7.5.2.- (characterized)
to candidate GFF1357 Psest_1392 ABC-type uncharacterized transport systems, ATPase components

Query= SwissProt::Q8G847
         (513 letters)



>FitnessBrowser__psRCH2:GFF1357
          Length = 518

 Score =  235 bits (599), Expect = 3e-66
 Identities = 154/482 (31%), Positives = 253/482 (52%), Gaps = 26/482 (5%)

Query: 12  GITIEFPGVKALDGVDLTLYPGEVHALMGENGAGKSTMIKALTGVYKINAGSIMVDGKPQ 71
           GIT ++PG  A D +DL++ PGE+HAL+GENGAGKST++K + GV + +AG I   G+  
Sbjct: 13  GITKQYPGCLANDRIDLSIQPGEIHALLGENGAGKSTLMKIIYGVTQPDAGEIHWQGERV 72

Query: 72  QFNGTLDAQNAGIATVYQEVNLCTNLSVGENV--MLGHEKRGPFGIDWKKTHEAAKKYLA 129
                  A+  GI  V+Q  +L   LSV EN+   LG +   P  ++  K  E +++Y  
Sbjct: 73  TMRDPAQARERGIGMVFQHFSLFETLSVAENIALALGAKAGTPKQLE-PKIREVSQRY-- 129

Query: 130 QMGLESIDPHTPLSSISIAMQQLVAIARAMVINAKVLILDEPTSSLDANEVRDLFAIMRK 189
             G+  ++P   + S+SI  +Q V I R ++ + ++LILDEPTS L   E  +LF  +R+
Sbjct: 130 --GM-PLEPQRLVHSLSIGERQRVEIIRCLMQDIRLLILDEPTSVLTPQEADELFVTLRR 186

Query: 190 VRDSGVAILFVSHFLDQIYEITDRLTILRNGQFIKEVMTKDTPRDELIGMMIGKSAAELS 249
           +   G +ILF+SH L+++  +    T+LR G+   E +  +    EL  +M+G +     
Sbjct: 187 LAAEGCSILFISHKLNEVRALCQSATVLRAGRVSGECIPAECSDLELARLMVGDAE---- 242

Query: 250 QIGAKKARREITPGEKPIVDVKGLGKKG------TINPVDVDIYKGEVVGFAGLLGSGRT 303
                +A    + G  P + V+ L          ++  VD+++  GE+VG AG+ G+G+ 
Sbjct: 243 ---GLEAEYPKSEGRAPFLRVERLSWHNADPFGVSLKEVDLEVRAGEIVGIAGVAGNGQD 299

Query: 304 ELGRLLYGADKPDSG---TYTLNGKKVNISDPYTALKNKIAYSTENRRDEGIIGDLTVRQ 360
           EL  LL G  +  +         G  V    P    ++ +A+    R   G +  +++  
Sbjct: 300 ELLALLSGEQRLQAAQAMRIRFLGDDVAHLRPGARRRHGMAFVPAERLGHGAVPSMSLAD 359

Query: 361 NILIALQATRGMFKP--IPKKEADAIVDKYMKELNVRPADPDRPVKNLSGGNQQKVLIGR 418
           N L+      GM +   I +    A  ++ ++   V+  D   P  +LSGGN QK ++GR
Sbjct: 360 NGLLTAYQQTGMVEQGLIRRGRVRAFAEQVIQRFAVKTPDAQTPAASLSGGNLQKFILGR 419

Query: 419 WLATHPELLILDEPTRGIDIGAKAEIQQVVLDLASQGMGVVFISSELEEVVRLSDDIEVL 478
            +   P+LLI   PT G+D+GA A I + +++L   G  ++ IS +LEE+ ++SD I  L
Sbjct: 420 EILQQPKLLIAAHPTWGVDVGAAAAIHRALIELRDAGAAILVISEDLEELFQISDRIAAL 479

Query: 479 KD 480
            D
Sbjct: 480 SD 481



 Score = 62.8 bits (151), Expect = 3e-14
 Identities = 55/248 (22%), Positives = 107/248 (43%), Gaps = 42/248 (16%)

Query: 22  ALDGVDLTLYPGEVHALMGENGAGKSTMIKALTGVYKINAGSIM---------------- 65
           +L  VDL +  GE+  + G  G G+  ++  L+G  ++ A   M                
Sbjct: 274 SLKEVDLEVRAGEIVGIAGVAGNGQDELLALLSGEQRLQAAQAMRIRFLGDDVAHLRPGA 333

Query: 66  -----VDGKPQQFNG-----TLDAQNAGIATVYQEVNLCTNLSVGENVMLGHEKRGPFGI 115
                +   P +  G     ++   + G+ T YQ+  +         V  G  +RG    
Sbjct: 334 RRRHGMAFVPAERLGHGAVPSMSLADNGLLTAYQQTGM---------VEQGLIRRG---- 380

Query: 116 DWKKTHEAAKKYLAQMGLESIDPHTPLSSISIAMQQLVAIARAMVINAKVLILDEPTSSL 175
              +    A++ + +  +++ D  TP +S+S    Q   + R ++   K+LI   PT  +
Sbjct: 381 ---RVRAFAEQVIQRFAVKTPDAQTPAASLSGGNLQKFILGREILQQPKLLIAAHPTWGV 437

Query: 176 DANEVRDLFAIMRKVRDSGVAILFVSHFLDQIYEITDRLTILRNGQFIKEVMTKDTPRDE 235
           D      +   + ++RD+G AIL +S  L+++++I+DR+  L +G+   +  T  T   E
Sbjct: 438 DVGAAAAIHRALIELRDAGAAILVISEDLEELFQISDRIAALSDGRLSPQRATASTCPVE 497

Query: 236 LIGMMIGK 243
           +   M G+
Sbjct: 498 VGRWMAGQ 505


Lambda     K      H
   0.316    0.135    0.376 

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: 567
Number of extensions: 24
Number of successful extensions: 8
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: 513
Length of database: 518
Length adjustment: 35
Effective length of query: 478
Effective length of database: 483
Effective search space:   230874
Effective search space used:   230874
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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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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
the source code
instructions for running GapMind on your computer

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