GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Acidovorax sp. GW101-3H11

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate Ac3H11_4180 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= reanno::Smeli:SM_b21216
         (360 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4180
          Length = 367

 Score =  228 bits (581), Expect = 2e-64
 Identities = 126/305 (41%), Positives = 187/305 (61%), Gaps = 14/305 (4%)

Query: 9   IRKRY-GEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDILIGERSV 67
           ++K Y GE   ++ +D+ ++ GEFL LLG SG GK+T L ++AG   P+ GDIL+  + +
Sbjct: 14  VQKTYDGEQLVVRALDLDIQRGEFLSLLGPSGSGKTTTLMMLAGFESPTAGDILLDGKQI 73

Query: 68  LGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARLLQIENLL 127
               P  R+  MVFQ+YAL+P+L+V  N+ + L +R+VP+AE  + V+    ++++  + 
Sbjct: 74  TRTPPHKRNFGMVFQNYALFPHLTVGENVAYPLTVRKVPKAEQAERVKKALDMVRLTGMA 133

Query: 128 DRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLHQMLRTTV 187
           DR P++LSGGQ+QRVA+ RALV NPQ+ L DEPL  LD +LR  M+ ELK LH+ L  T 
Sbjct: 134 DRLPARLSGGQQQRVALARALVFNPQLVLMDEPLGALDKQLREHMQIELKELHRQLGVTF 193

Query: 188 VYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMNILDAEMT 247
           VYVTHDQ EA+T++ R+AV  +G I+QLA  + +Y+ P+  +VAGFVG       D+ + 
Sbjct: 194 VYVTHDQGEALTMSDRVAVFNEGVIQQLADVESLYETPSNRFVAGFVG-------DSTVL 246

Query: 248 ANGLKIEGCEEVLPLPAAF------NGAAWAGRRVKVGIRPEALRLAAGSEAQRLTASVE 301
           +  L+  G +  + +P  F         A  G RV+  +RPE + L   SE  R  A   
Sbjct: 247 SGTLQGAGADAAIQMPGGFLLPGVNVNQAPVGARVQACVRPERVVLLPQSEYPRPNAIPA 306

Query: 302 VVELT 306
            V  T
Sbjct: 307 TVART 311


Lambda     K      H
   0.320    0.136    0.385 

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: 318
Number of extensions: 11
Number of successful extensions: 2
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: 360
Length of database: 367
Length adjustment: 29
Effective length of query: 331
Effective length of database: 338
Effective search space:   111878
Effective search space used:   111878
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