Alignments for a candidate for araVsh in Azospirillum brasilense Sp245

GapMind for catabolism of small carbon sources

Alignments for a candidate for araVsh in Azospirillum brasilense Sp245

Align ABC transporter related (characterized, see rationale)
to candidate AZOBR_RS31245 AZOBR_RS31245 ABC transporter ATP-binding protein

Query= uniprot:A0KWY5
         (499 letters)



>FitnessBrowser__azobra:AZOBR_RS31245
          Length = 518

 Score =  323 bits (829), Expect = 7e-93
 Identities = 189/506 (37%), Positives = 306/506 (60%), Gaps = 19/506 (3%)

Query: 4   ILELKQISKHYPGVKALEDVSLRLFAGEVHALLGENGAGKSTLVKVMTGA--QSKDMGDI 61
           ILE+K I+K +PGVKAL+DV+L +  GE+HAL+GENGAGKSTL+KV++G   Q    G+I
Sbjct: 5   ILEMKGITKTFPGVKALDDVNLSVREGEIHALIGENGAGKSTLMKVLSGVYPQGSFDGEI 64

Query: 62  LFLGEPQHFNTPMDAQKAGISTVYQEVNLVPNLTVAQNLFLGYEPRRLGLIHFKKMYADA 121
            F G+PQ F    D+++ GI  ++QE+ LVP L++ +NLFLG E    G+I +      A
Sbjct: 65  RFRGQPQAFRGIADSERLGIIIIHQELALVPLLSITENLFLGNEQASRGVIDWDAATLRA 124

Query: 122 RAVLTQFKLDIDVSAPLSDYSIAVQQLIAIARGVAMSAKVLVLDEPTASLDAKEVQVLFG 181
           R +L    L       ++D  +  QQL+ IA+ ++   K+L+LDEPTASL+  +   L  
Sbjct: 125 RELLRLVGLHDPPETLITDIGVGKQQLVEIAKALSKEVKLLILDEPTASLNESDSDALLE 184

Query: 182 ILNQLKAKGVAIVFITHFLDQVYQISDRITVLRNGQFIG--EYLTAELPQPKLIEAMLGR 239
           +L Q KA+G+A + I+H L+++ +++DR+T+LR+G  +   +   A + Q ++I  M+GR
Sbjct: 185 LLLQFKARGIASILISHKLNEIAKVADRVTILRDGTTVETLDCREAVVSQDRIIRGMVGR 244

Query: 240 SLQEQLVDKQEKERTVTRAEAVLLSLEDVSV-------KGSIQSMNLTVPKGQAVGLAGL 292
           +L ++        R  T    VL  ++  S        +  ++ +NLTV +G+ VG+AGL
Sbjct: 245 ALSDRY------PRRTTVPGDVLFEVKGWSADHPAHPGRRVVRDVNLTVRRGEVVGIAGL 298

Query: 293 LGSGRSEVCNAVFGLDLVDS--GSIHLAGQKLNLSQPVDAISAGIALCPEDRKIDGIIGP 350
           +G+GR+E   ++FG     +  G   L G+++++S    A++ G+A   EDRK  G++  
Sbjct: 299 MGAGRTEFAMSLFGRSYGRNIRGQAFLDGREIDVSTISRAMANGLAYATEDRKHLGLVLD 358

Query: 351 LSIRENIILALQARIGWWRYLSNTRQQEIAQFFIDKLQIATPDADKPIEQLSGGNQQKVI 410
             IR N+ LA    +     + + R+ ++A+ F  +L+I   D  +    LSGGNQQKV+
Sbjct: 359 NDIRHNVTLANLRGVAKRWVIDHEREVQVAEEFRRRLRIRCADVFQETVNLSGGNQQKVV 418

Query: 411 LARWLAIEPILLVLDEPTRGIDIGAHAEIVKLIRTLCDEGMSLLVASSELDELVAFSNKV 470
           L++WL  +P +L+LDEPTRGID+GA  EI  +I  L  EG  +++ SSE+ EL+  ++++
Sbjct: 419 LSKWLFADPQVLILDEPTRGIDVGAKYEIYTIINQLVAEGRGVVLISSEMPELLGVADRI 478

Query: 471 VVLRDRYAVRELSGAELTSQHVMQAI 496
            V+     V E+  AE + + +M AI
Sbjct: 479 YVMNAGEMVAEMPAAEASQEKIMGAI 504



 Score = 69.7 bits (169), Expect = 2e-16
 Identities = 61/249 (24%), Positives = 109/249 (43%), Gaps = 42/249 (16%)

Query: 14  YPGVKALEDVSLRLFAGEVHALLGENGAGKSTLVKVMTGAQSKDMGDILFLGEPQHFNTP 73
           +PG + + DV+L +  GEV  + G  GAG++     + G            G        
Sbjct: 274 HPGRRVVRDVNLTVRRGEVVGIAGLMGAGRTEFAMSLFGRS---------YGRNIRGQAF 324

Query: 74  MDAQKAGISTVYQEVNLVPNLTVAQNLFLGYEPRR-LGL-----IHFKKMYADARAVLTQ 127
           +D ++  +ST+ +         +A  L    E R+ LGL     I      A+ R V  +
Sbjct: 325 LDGREIDVSTISR--------AMANGLAYATEDRKHLGLVLDNDIRHNVTLANLRGVAKR 376

Query: 128 FKLD-------------------IDVSAPLSDYSIAVQQLIAIARGVAMSAKVLVLDEPT 168
           + +D                    DV     + S   QQ + +++ +    +VL+LDEPT
Sbjct: 377 WVIDHEREVQVAEEFRRRLRIRCADVFQETVNLSGGNQQKVVLSKWLFADPQVLILDEPT 436

Query: 169 ASLDAKEVQVLFGILNQLKAKGVAIVFITHFLDQVYQISDRITVLRNGQFIGEYLTAELP 228
             +D      ++ I+NQL A+G  +V I+  + ++  ++DRI V+  G+ + E   AE  
Sbjct: 437 RGIDVGAKYEIYTIINQLVAEGRGVVLISSEMPELLGVADRIYVMNAGEMVAEMPAAEAS 496

Query: 229 QPKLIEAML 237
           Q K++ A++
Sbjct: 497 QEKIMGAIM 505


Lambda     K      H
   0.319    0.136    0.377 

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: 606
Number of extensions: 27
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: 499
Length of database: 518
Length adjustment: 34
Effective length of query: 465
Effective length of database: 484
Effective search space:   225060
Effective search space used:   225060
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
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