GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bgtB' in Marinobacter adhaerens HP15

Align ABC-type permease for basic amino acids and glutamine (characterized, see rationale)
to candidate GFF2245 HP15_2195 amino acid ABC transporter, permease protein

Query= uniprot:Q31RP0
         (377 letters)



>FitnessBrowser__Marino:GFF2245
          Length = 395

 Score =  255 bits (651), Expect = 2e-72
 Identities = 151/369 (40%), Positives = 216/369 (58%), Gaps = 15/369 (4%)

Query: 12  WRDERLWRWVWQLLVLLVVGLGAIWLVDNLVYNLSQRGLSLSFDWLDQSAGFNIGESAIA 71
           W D R+    +Q + + +V  G   LVDN + N+  RG+S  F +L ++AGF I  + + 
Sbjct: 16  WYDPRVRSLFFQAVAIALVFWGGWILVDNTLSNMESRGISTGFGFLGETAGFGIIMNLVP 75

Query: 72  YRTADSYARALVVGLVNSLRVIAIGLILTTVIGTLAGVAAFSENWLLRQLSRGYVAVVRN 131
           Y    SY R   VGL N+L V A+G++  T++G + GVA  S NWL+ +++  Y+ V+RN
Sbjct: 76  YDATMSYGRTFWVGLTNTLLVSAMGVVAATILGFIIGVARLSSNWLVAKMALVYIEVIRN 135

Query: 132 TPLLLQLIVWYFPILLSLPAAQQPWHWLGSLYLSKQGIYLPWPQTPG-----WLVVILAI 186
            PLLLQ+  WYF +L +LP+ +Q     G+L+L+ +G+YLP P T       W  ++LAI
Sbjct: 136 IPLLLQIFFWYFAVLSNLPSPRQSVDVGGALFLNNRGLYLPDPVTQEGFGIVWGGILLAI 195

Query: 187 ALVLFVS-WLAQRQRSP-------RDWRWLYGAIAVVTVLMLLTQLSWP-QQLQPGQIRG 237
           A V+ +  W  +RQ +        +    +   + +++ L+    L W    L+     G
Sbjct: 196 AAVVGIRIWAKKRQLATGQIFPTFKVGVAILVLVPIISYLVAGRPLEWDLPALRGFNFGG 255

Query: 238 GLRLSLEFTALLLGLVAYTGAFITEIIRGGILSVPAGQWEAAAALGLTRSQTLWQIVVPQ 297
           G+ +  E  AL + L  YT +FI EI+R GILSV  GQ EA+ ALGL    TL  +V+PQ
Sbjct: 256 GITIIPELAALWIALSLYTASFIAEIVRSGILSVSKGQTEASKALGLPNGLTLRLVVIPQ 315

Query: 298 ALRVIVPSLNSQYVGFAKNSSLAIAVGYPDLYATAQ-TTLNQTGRPVEVFLILMLTYLAI 356
           A+RVI+P L SQY+   KNSSLA A+GYPDL A    TTLNQTG+ VEV  I M  YL I
Sbjct: 316 AMRVIIPPLTSQYLNLVKNSSLATAIGYPDLVAVFMGTTLNQTGQAVEVVAITMAVYLTI 375

Query: 357 NAVISAGMN 365
           + +IS  MN
Sbjct: 376 SLLISLFMN 384


Lambda     K      H
   0.326    0.140    0.445 

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: 429
Number of extensions: 31
Number of successful extensions: 3
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: 377
Length of database: 395
Length adjustment: 30
Effective length of query: 347
Effective length of database: 365
Effective search space:   126655
Effective search space used:   126655
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 50 (23.9 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