Alignments for a candidate for fruK in Azospirillum brasilense Sp245

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruK in Azospirillum brasilense Sp245

Align Fructose import ATP-binding protein FruK; EC 7.5.2.- (characterized)
to candidate AZOBR_RS31210 AZOBR_RS31210 sugar ABC transporter ATP-binding protein

Query= SwissProt::Q8G847
         (513 letters)



>FitnessBrowser__azobra:AZOBR_RS31210
          Length = 516

 Score =  448 bits (1153), Expect = e-130
 Identities = 236/506 (46%), Positives = 339/506 (66%), Gaps = 2/506 (0%)

Query: 2   TDKNPIVVMKGITIEFPGVKALDGVDLTLYPGEVHALMGENGAGKSTMIKALTGVYKINA 61
           T   P++ ++G++  F GV+ALDGVD T+  GE+HAL+GENGAGKST+IK LTGVY+ +A
Sbjct: 7   TASPPLLAIRGLSKAFLGVQALDGVDFTVRHGEIHALLGENGAGKSTLIKTLTGVYQRDA 66

Query: 62  GSIMVDGKPQQFNGTLDAQNAGIATVYQEVNLCTNLSVGENVMLGHEKRGPFGIDWKKTH 121
           G++ ++G+     G  +AQ   I TVYQEVNL  NLSV EN+ LG +      +D     
Sbjct: 67  GTVTLEGRAIAPRGVEEAQRLHIGTVYQEVNLLPNLSVAENLFLGRQPMRFGLVDRGAMR 126

Query: 122 EAAKKYLAQMGLESIDPHTPLSSISIAMQQLVAIARAMVINAKVLILDEPTSSLDANEVR 181
             A+  L   GL ++D   PL   S+A QQ+VAIARA+ ++AKVLILDEPT+SLDA EV 
Sbjct: 127 RRARAVLIPYGL-TLDVTAPLGRFSVATQQIVAIARAVDMSAKVLILDEPTASLDAQEVA 185

Query: 182 DLFAIMRKVRDSGVAILFVSHFLDQIYEITDRLTILRNGQFIKEVMTKDTPRDELIGMMI 241
            LF +MR +R  G+ I+FV+HFLDQ+Y + DR+T+LRNG+ + E  T + PR +L+ MM+
Sbjct: 186 VLFKVMRTLRSRGIGIVFVTHFLDQVYALCDRITVLRNGRLVGERRTAELPRLDLVAMML 245

Query: 242 GKSAAELSQIGAKKARREITPGEKPIVDVKGLGKKGTINPVDVDIYKGEVVGFAGLLGSG 301
           G+    ++   A  A         P+V  +G GK  ++ P D+DI  GEVVG AGLLGSG
Sbjct: 246 GRELEAVAHRIAPPADDAEEDARPPLVRFRGYGKARSVEPFDLDIRPGEVVGLAGLLGSG 305

Query: 302 RTELGRLLYGADKPDSGTYTLNGKKVNISDPYTALKNKIAYSTENRRDEGIIGDLTVRQN 361
           RTE  RL++G D+ D G   ++G+ V +  P  A++    +  E+R+ EGI+G L+VR+N
Sbjct: 306 RTETARLVFGMDRADRGEAAVDGQAVRLRGPRDAIRLGFGFCPEDRKKEGIVGALSVREN 365

Query: 362 ILIALQATRGMFKPIPKKEADAIVDKYMKELNVRPADPDRPVKNLSGGNQQKVLIGRWLA 421
           I++ALQA +G  +PIP+   + I D++++ L++R    ++P++ LSGGNQQK L+ RWLA
Sbjct: 366 IILALQARQGWLRPIPRCRQEEIADRFIRLLDIRTPHAEQPIQLLSGGNQQKALLARWLA 425

Query: 422 THPELLILDEPTRGIDIGAKAEIQQVVLDLASQGMGVVFISSELEEVVRLSDDIEVLKDR 481
           T P LLILDEPTRGID+GA AEI +++  L + GM ++ +SSELEE+V  S  + VL+DR
Sbjct: 426 TEPRLLILDEPTRGIDVGAHAEIIRLIERLCADGMALLVVSSELEEIVAYSRRVVVLRDR 485

Query: 482 HKIAEIENDDTVSQATIVETIANTNV 507
             +AE+   + V+   IV  IA+ +V
Sbjct: 486 RHVAELRGGE-VAVDRIVAAIASESV 510



 Score = 89.0 bits (219), Expect = 4e-22
 Identities = 60/247 (24%), Positives = 121/247 (48%), Gaps = 9/247 (3%)

Query: 6   PIVVMKGITIEFPGVKALDGVDLTLYPGEVHALMGENGAGKSTMIKALTGVYKINAGSIM 65
           P+V  +G    +   ++++  DL + PGEV  L G  G+G++   + + G+ + + G   
Sbjct: 270 PLVRFRG----YGKARSVEPFDLDIRPGEVVGLAGLLGSGRTETARLVFGMDRADRGEAA 325

Query: 66  VDGKPQQFNGTLDAQNAGIATVYQE---VNLCTNLSVGENVMLGHEKRGPF--GIDWKKT 120
           VDG+  +  G  DA   G     ++     +   LSV EN++L  + R  +   I   + 
Sbjct: 326 VDGQAVRLRGPRDAIRLGFGFCPEDRKKEGIVGALSVRENIILALQARQGWLRPIPRCRQ 385

Query: 121 HEAAKKYLAQMGLESIDPHTPLSSISIAMQQLVAIARAMVINAKVLILDEPTSSLDANEV 180
            E A +++  + + +     P+  +S   QQ   +AR +    ++LILDEPT  +D    
Sbjct: 386 EEIADRFIRLLDIRTPHAEQPIQLLSGGNQQKALLARWLATEPRLLILDEPTRGIDVGAH 445

Query: 181 RDLFAIMRKVRDSGVAILFVSHFLDQIYEITDRLTILRNGQFIKEVMTKDTPRDELIGMM 240
            ++  ++ ++   G+A+L VS  L++I   + R+ +LR+ + + E+   +   D ++  +
Sbjct: 446 AEIIRLIERLCADGMALLVVSSELEEIVAYSRRVVVLRDRRHVAELRGGEVAVDRIVAAI 505

Query: 241 IGKSAAE 247
             +S  E
Sbjct: 506 ASESVPE 512


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: 693
Number of extensions: 21
Number of successful extensions: 6
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: 516
Length adjustment: 35
Effective length of query: 478
Effective length of database: 481
Effective search space:   229918
Effective search space used:   229918
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