Aligments for a candidate for frcA in Azospirillum brasilense Sp245

GapMind for catabolism of small carbon sources

Aligments for a candidate for frcA in Azospirillum brasilense Sp245

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

Query= SwissProt::Q9F9B0
         (260 letters)



>FitnessBrowser__azobra:AZOBR_RS31210
          Length = 516

 Score =  159 bits (403), Expect = 9e-44
 Identities = 97/248 (39%), Positives = 145/248 (58%), Gaps = 9/248 (3%)

Query: 2   AQEPILTARGLVKRYGRVTALDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPDEG 61
           A  P+L  RGL K +  V ALD  DF +  GEI A++G+NGAGKS++IK ++G    D G
Sbjct: 8   ASPPLLAIRGLSKAFLGVQALDGVDFTVRHGEIHALLGENGAGKSTLIKTLTGVYQRDAG 67

Query: 62  EIRLEGKPIQFRSPMEARQAGIETVYQNLALSPALSIADNMFLGREIRKPGIMGKWFRSL 121
            + LEG+ I  R   EA++  I TVYQ + L P LS+A+N+FLGR+  + G+       +
Sbjct: 68  TVTLEGRAIAPRGVEEAQRLHIGTVYQEVNLLPNLSVAENLFLGRQPMRFGL-------V 120

Query: 122 DRAAMEKQARAKLSELGLMTIQNINQAVETLSGGQRQGVAVARAAAFGSKVVIMDEPTAA 181
           DR AM ++ARA L   GL    ++   +   S   +Q VA+ARA    +KV+I+DEPTA+
Sbjct: 121 DRGAMRRRARAVLIPYGLTL--DVTAPLGRFSVATQQIVAIARAVDMSAKVLILDEPTAS 178

Query: 182 LGVKESRRVLELILDVRRRGLPIVLISHNMPHVFEVADRIHIHRLGRRLCVINPKDYTMS 241
           L  +E   + +++  +R RG+ IV ++H +  V+ + DRI + R GR +      +    
Sbjct: 179 LDAQEVAVLFKVMRTLRSRGIGIVFVTHFLDQVYALCDRITVLRNGRLVGERRTAELPRL 238

Query: 242 DAVAFMTG 249
           D VA M G
Sbjct: 239 DLVAMMLG 246



 Score = 92.4 bits (228), Expect = 2e-23
 Identities = 61/255 (23%), Positives = 124/255 (48%), Gaps = 13/255 (5%)

Query: 2   AQEPILTARGLVKRYGRVTALDRADFDLYPGEILAVIGDNGAGKSSMIKAISGAVTPDEG 61
           A+ P++  RG    YG+  +++  D D+ PGE++ + G  G+G++   + + G    D G
Sbjct: 267 ARPPLVRFRG----YGKARSVEPFDLDIRPGEVVGLAGLLGSGRTETARLVFGMDRADRG 322

Query: 62  EIRLEGKPIQFRSPMEARQAGIETVYQNL---ALSPALSIADNMFLGREIRKPGIMGKWF 118
           E  ++G+ ++ R P +A + G     ++     +  ALS+ +N+ L  + R+      W 
Sbjct: 323 EAAVDGQAVRLRGPRDAIRLGFGFCPEDRKKEGIVGALSVRENIILALQARQ-----GWL 377

Query: 119 RSLDRAAMEKQARAKLSELGLMTIQNINQAVETLSGGQRQGVAVARAAAFGSKVVIMDEP 178
           R + R   E+ A   +  L + T  +  Q ++ LSGG +Q   +AR  A   +++I+DEP
Sbjct: 378 RPIPRCRQEEIADRFIRLLDIRT-PHAEQPIQLLSGGNQQKALLARWLATEPRLLILDEP 436

Query: 179 TAALGVKESRRVLELILDVRRRGLPIVLISHNMPHVFEVADRIHIHRLGRRLCVINPKDY 238
           T  + V     ++ LI  +   G+ ++++S  +  +   + R+ + R  R +  +   + 
Sbjct: 437 TRGIDVGAHAEIIRLIERLCADGMALLVVSSELEEIVAYSRRVVVLRDRRHVAELRGGEV 496

Query: 239 TMSDAVAFMTGAKEP 253
            +   VA +     P
Sbjct: 497 AVDRIVAAIASESVP 511


Lambda     K      H
   0.321    0.136    0.383 

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: 334
Number of extensions: 21
Number of successful extensions: 5
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: 260
Length of database: 516
Length adjustment: 29
Effective length of query: 231
Effective length of database: 487
Effective search space:   112497
Effective search space used:   112497
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: 49 (23.5 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