GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Pseudomonas stutzeri RCH2

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate GFF3990 Psest_4063 sulfate ABC transporter, ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_2941
         (350 letters)



>FitnessBrowser__psRCH2:GFF3990
          Length = 334

 Score =  226 bits (577), Expect = 5e-64
 Identities = 127/324 (39%), Positives = 193/324 (59%), Gaps = 26/324 (8%)

Query: 4   LQLRGIEKFFGEHRAIKGIDLTIQQGEFIVFVGPSGCGKSTLLRLIAGLEAIDGGSLMLD 63
           +++  I K FG+ +A+  I+L IQ GE +  +GPSGCGK++LLR+IAGLE  D GS++  
Sbjct: 3   IEISHINKRFGQFQALNTINLHIQSGELVALLGPSGCGKTSLLRIIAGLETPDSGSIVFH 62

Query: 64  GRDITDQPSSKRDLAMVFQSYALYPHMSVYENMSFALKLA----KVDKQVIDEKVQNAAR 119
           G D++ +    R++  VFQ YAL+ HM+V+EN++F L++     +  + VI EKV     
Sbjct: 63  GEDVSSRDVRDRNVGFVFQHYALFRHMTVFENVAFGLRMKPKKQRPSEAVIAEKVHELLG 122

Query: 120 ILNLTQYLQRTPKELSGGQRQRVAIGRAIVRAPKVFLFDEPLSNLDAALRGQTRVEIAKL 179
           ++ L     R P++LSGGQRQR+A+ RA+   PKV L DEP   LDA +R + R  +A+L
Sbjct: 123 LVQLDWLADRYPEQLSGGQRQRIALARALAVEPKVLLLDEPFGALDAKVRKELRRWLARL 182

Query: 180 HRDLGATTIYVTHDQVEAMTLADRVVVLRDGIIEQVGTPLELYDKPANQFVAQFIGTPQM 239
           H D+  T+++VTHDQ EAM +ADR+VV+  G+IEQ+GTP E+Y  PA++FV  F+G    
Sbjct: 183 HEDVHLTSVFVTHDQEEAMEVADRIVVMNKGVIEQIGTPAEVYANPASEFVYDFLG---- 238

Query: 240 NVVPVDKLPQPVQQQAPAAPAGAAVGAIGLRPENITV-RTTGATPVGGQVDLIEALGAET 298
                ++L    Q+            ++  RP  + + R   A  + G+V  I  LGA T
Sbjct: 239 ---DANRLQLDDQR------------SVLFRPHEVALSREAVAEHLAGEVRDIRPLGALT 283

Query: 299 LIYVTTPGGAQFVSRQ--NDRTDL 320
            + +   G A+ +  +  ND   L
Sbjct: 284 RVTLKVAGQAEPIEAEVGNDHASL 307


Lambda     K      H
   0.320    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: 289
Number of extensions: 12
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: 350
Length of database: 334
Length adjustment: 29
Effective length of query: 321
Effective length of database: 305
Effective search space:    97905
Effective search space used:    97905
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.

Links

Downloads

Related tools

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