GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Azospirillum brasilense Sp245

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate AZOBR_RS25335 AZOBR_RS25335 putative ABC transporter (ATP-binding protein)

Query= reanno::Smeli:SM_b21106
         (365 letters)



>FitnessBrowser__azobra:AZOBR_RS25335
          Length = 365

 Score =  261 bits (668), Expect = 2e-74
 Identities = 154/363 (42%), Positives = 209/363 (57%), Gaps = 22/363 (6%)

Query: 1   MAPVTLKKLVKRYG-ALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGA 59
           + P+ L +L KRYG A   +  + LEV   E + LVGPSGCGK+T LR+IAGL   SGG 
Sbjct: 7   LVPLALDRLAKRYGTAPPALAALSLEVAGGELLGLVGPSGCGKTTALRLIAGLTPASGGR 66

Query: 60  IEIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAA 119
           + +GGR +  LP  AR I +VFQ+YAL+PHMT A+N+ F L++ G PA E   R AEA A
Sbjct: 67  VLVGGRDITALPAHARGIGLVFQNYALFPHMTAADNVAFGLRMRGLPAAERHARTAEALA 126

Query: 120 ILDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKL 179
           ++ L+HL  R+P  LSGGQ+QRVA+ RA+  +P++ L DEPLSNLDA LR ++  EI+ L
Sbjct: 127 MVRLSHLGGRKPRALSGGQQQRVALARALAIRPNLLLLDEPLSNLDAGLRAELLAEIRTL 186

Query: 180 HARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPM 239
             R+  T ++VTHDQ EA+ + DRI ++RDG +EQVGTP +V  RPA+ FVAGF+G    
Sbjct: 187 QRRLGITALFVTHDQGEALAVCDRIAVLRDGRLEQVGTPREVHDRPASGFVAGFVGR--T 244

Query: 240 NMEEAVLTDGKLAFASGATLPLPPRFRSLVREGQKVTFGLRPDDVYPSGHGLHAGDADAV 299
           N   A    G      G  LP        + +G        P D++   H +  G A   
Sbjct: 245 NRIPAERLAGGALRVGGTLLP-------ALADGP-----AGPVDLFVRPHRIRVGAAGGA 292

Query: 300 HEIELPVTITEPLGNETLVFTQFNGR----DWVSRMLNPRP---LRPGEAVPMSFDLARA 352
             +   +  T  LG+   +  +  G     DW      P P   L PGE V +S+D A  
Sbjct: 293 GGLPAVLRGTAFLGDRIALSLEAGGAPVTVDWPVEAAPPAPGPALTPGETVALSWDPADM 352

Query: 353 HLF 355
            +F
Sbjct: 353 AVF 355


Lambda     K      H
   0.320    0.137    0.397 

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: 425
Number of extensions: 23
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 365
Length of database: 365
Length adjustment: 30
Effective length of query: 335
Effective length of database: 335
Effective search space:   112225
Effective search space used:   112225
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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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:

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:

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:

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:

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