GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Azospirillum brasilense Sp245

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate AZOBR_RS30410 AZOBR_RS30410 ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__azobra:AZOBR_RS30410
          Length = 371

 Score =  246 bits (629), Expect = 5e-70
 Identities = 145/334 (43%), Positives = 203/334 (60%), Gaps = 14/334 (4%)

Query: 1   MTSVSVR--DLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDG 58
           M SV VR   + L++G+  VL  ++LDI  GEF   LG SGCGK+TLL  IAG      G
Sbjct: 14  MESVGVRIDGVDLSYGSHRVLKDIHLDIKPGEFFAFLGPSGCGKTTLLRLIAGFNTAQRG 73

Query: 59  QIFIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRAS 118
            + I  R+++      R +GMVFQSYAL+P MTV +N++FGL+  ++P AEIE+RV  A 
Sbjct: 74  AVTIGGRDISGLPAHKRDVGMVFQSYALWPHMTVRRNVAFGLEERRVPRAEIERRVDAAL 133

Query: 119 EILQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKR 178
           +++ ++ L  R+PS+LSGGQ+QRVA+ R +V +  V L DEPLSNLDAKLR ++R E+  
Sbjct: 134 DLVGLKHLADRRPSQLSGGQQQRVALARTIVIEPKVLLLDEPLSNLDAKLRVQMRQELLS 193

Query: 179 LHQSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPS 238
           L + L  T I+VTHDQ EA T+ DRIAVM+ G++QQ+  P  +Y+ P NLFVAGF+G  +
Sbjct: 194 LQRKLGLTTIFVTHDQEEANTICDRIAVMEDGIVQQVGTPQELYDHPANLFVAGFLG--T 251

Query: 239 MNFFRGEVEPKD-GRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDE----A 293
            N   G+V   D G +FV  GG+       P    ++PG    L  RP+++ + +     
Sbjct: 252 ANVLEGQVRAVDGGTAFVMGGGVPI-----PLPHGVEPGAAGKLMFRPQNLFIRQDGGPP 306

Query: 294 RDGEPTHQAVVDIEEPMGADNLLWLTFAGQSMSV 327
           R G      VV   E +GA     +   GQ + V
Sbjct: 307 RAGHVRLMGVVRHREFLGASIRYAVDIGGQQVQV 340


Lambda     K      H
   0.320    0.137    0.392 

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: 390
Number of extensions: 17
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: 361
Length of database: 371
Length adjustment: 30
Effective length of query: 331
Effective length of database: 341
Effective search space:   112871
Effective search space used:   112871
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