Alignments for a candidate for mglA in Azospirillum brasilense Sp245

GapMind for catabolism of small carbon sources

Alignments for a candidate for mglA in Azospirillum brasilense Sp245

Align Galactose/methyl galactoside import ATP-binding protein MglA; EC 7.5.2.11 (characterized)
to candidate AZOBR_RS31245 AZOBR_RS31245 ABC transporter ATP-binding protein

Query= SwissProt::P23924
         (506 letters)



>FitnessBrowser__azobra:AZOBR_RS31245
          Length = 518

 Score =  357 bits (915), Expect = e-103
 Identities = 198/498 (39%), Positives = 303/498 (60%), Gaps = 12/498 (2%)

Query: 13  LLEMRGINKSFPGVKALDNVNLNVRPHSIHALMGENGAGKSTLLKCLFGIYQKDS--GSI 70
           +LEM+GI K+FPGVKALD+VNL+VR   IHAL+GENGAGKSTL+K L G+Y + S  G I
Sbjct: 5   ILEMKGITKTFPGVKALDDVNLSVREGEIHALIGENGAGKSTLMKVLSGVYPQGSFDGEI 64

Query: 71  VFQGKEVDFHSAKEALENGISMVHQELNLVLQRSVMDNMWLGRYPTKGMFVDQDKMYQDT 130
            F+G+   F    ++   GI ++HQEL LV   S+ +N++LG        +D D      
Sbjct: 65  RFRGQPQAFRGIADSERLGIIIIHQELALVPLLSITENLFLGNEQASRGVIDWDAATLRA 124

Query: 131 KAIFDELDIDIDPRARVGTLSVSQMQMIEIAKAFSYNAKIVIMDEPTSSLTEKEVNHLFT 190
           + +   + +   P   +  + V + Q++EIAKA S   K++I+DEPT+SL E + + L  
Sbjct: 125 RELLRLVGLHDPPETLITDIGVGKQQLVEIAKALSKEVKLLILDEPTASLNESDSDALLE 184

Query: 191 IIRKLKERGCGIVYISHKMEEIFQLCDEITILRDGQWIATQPLEG--LDMDKIIAMMVGR 248
           ++ + K RG   + ISHK+ EI ++ D +TILRDG  + T       +  D+II  MVGR
Sbjct: 185 LLLQFKARGIASILISHKLNEIAKVADRVTILRDGTTVETLDCREAVVSQDRIIRGMVGR 244

Query: 249 SLNQRFPDKENKPGDVILEVR-----HLTSLRQPSIRDVSFDLHKGEILGIAGLVGAKRT 303
           +L+ R+P +   PGDV+ EV+     H     +  +RDV+  + +GE++GIAGL+GA RT
Sbjct: 245 ALSDRYPRRTTVPGDVLFEVKGWSADHPAHPGRRVVRDVNLTVRRGEVVGIAGLMGAGRT 304

Query: 304 DIVETLFG--IREKSSGTITLHGKKINNHTANEAINHGFALVTEERRSTGIYAYLDIGFN 361
           +   +LFG        G   L G++I+  T + A+ +G A  TE+R+  G+    DI  N
Sbjct: 305 EFAMSLFGRSYGRNIRGQAFLDGREIDVSTISRAMANGLAYATEDRKHLGLVLDNDIRHN 364

Query: 362 SLISNIRNYKNKVGLLDNSRMKSDTQWVIDSMRVKTPGHRTQIGSLSGGNQQKVIIGRWL 421
             ++N+R    +  ++D+ R     +     +R++      +  +LSGGNQQKV++ +WL
Sbjct: 365 VTLANLRGVAKR-WVIDHEREVQVAEEFRRRLRIRCADVFQETVNLSGGNQQKVVLSKWL 423

Query: 422 LTQPEILMLDEPTRGIDVGAKFEIYQLIAELAKKGKGIIIISSEMPELLGITDRILVMSN 481
              P++L+LDEPTRGIDVGAK+EIY +I +L  +G+G+++ISSEMPELLG+ DRI VM+ 
Sbjct: 424 FADPQVLILDEPTRGIDVGAKYEIYTIINQLVAEGRGVVLISSEMPELLGVADRIYVMNA 483

Query: 482 GLVSGIVDTKTTTQNEIL 499
           G +   +     +Q +I+
Sbjct: 484 GEMVAEMPAAEASQEKIM 501



 Score = 89.7 bits (221), Expect = 2e-22
 Identities = 66/248 (26%), Positives = 118/248 (47%), Gaps = 11/248 (4%)

Query: 10  GEYLLEMRGINK---SFPGVKALDNVNLNVRPHSIHALMGENGAGKSTLLKCLFG-IYQK 65
           G+ L E++G +    + PG + + +VNL VR   +  + G  GAG++     LFG  Y +
Sbjct: 258 GDVLFEVKGWSADHPAHPGRRVVRDVNLTVRRGEVVGIAGLMGAGRTEFAMSLFGRSYGR 317

Query: 66  D-SGSIVFQGKEVDFHSAKEALENGISMVHQE---LNLVLQRSVMDNMWLG--RYPTKGM 119
           +  G     G+E+D  +   A+ NG++   ++   L LVL   +  N+ L   R   K  
Sbjct: 318 NIRGQAFLDGREIDVSTISRAMANGLAYATEDRKHLGLVLDNDIRHNVTLANLRGVAKRW 377

Query: 120 FVDQDKMYQDTKAIFDELDIDI-DPRARVGTLSVSQMQMIEIAKAFSYNAKIVIMDEPTS 178
            +D ++  Q  +     L I   D       LS    Q + ++K    + +++I+DEPT 
Sbjct: 378 VIDHEREVQVAEEFRRRLRIRCADVFQETVNLSGGNQQKVVLSKWLFADPQVLILDEPTR 437

Query: 179 SLTEKEVNHLFTIIRKLKERGCGIVYISHKMEEIFQLCDEITILRDGQWIATQPLEGLDM 238
            +       ++TII +L   G G+V IS +M E+  + D I ++  G+ +A  P      
Sbjct: 438 GIDVGAKYEIYTIINQLVAEGRGVVLISSEMPELLGVADRIYVMNAGEMVAEMPAAEASQ 497

Query: 239 DKIIAMMV 246
           +KI+  ++
Sbjct: 498 EKIMGAIM 505


Lambda     K      H
   0.319    0.137    0.388 

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: 679
Number of extensions: 35
Number of successful extensions: 11
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: 506
Length of database: 518
Length adjustment: 35
Effective length of query: 471
Effective length of database: 483
Effective search space:   227493
Effective search space used:   227493
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 (21.7 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