GapMind for catabolism of small carbon sources

 

Alignments for a candidate for yjtF in Paraburkholderia bryophila 376MFSha3.1

Align Inner membrane ABC transporter permease protein YjfF (characterized)
to candidate H281DRAFT_02176 H281DRAFT_02176 monosaccharide ABC transporter membrane protein, CUT2 family

Query= SwissProt::P37772
         (331 letters)



>FitnessBrowser__Burk376:H281DRAFT_02176
          Length = 321

 Score =  161 bits (407), Expect = 2e-44
 Identities = 111/316 (35%), Positives = 167/316 (52%), Gaps = 22/316 (6%)

Query: 2   IKRNLPLMIT-IGVFVLGYLYCLTQFPGFASTRVICNILTDNAFLGIIAVGMTFVILSGG 60
           +K+NLP+++  + + VLG    L ++  FAS   I +    N+   +I+VGM FVI++GG
Sbjct: 1   MKKNLPILLALVALVVLG----LVRYEHFASAYNITSFWRYNSMFALISVGMAFVIITGG 56

Query: 61  IDLSVGSVIAFTGVFLAKVIGDFGLSPLLAFPLVLVMGCAFGAFMGLLIDALKIPAFIIT 120
           IDLSVG+V A + V  A      G   ++A       G A G   G++I  LKI  FI+T
Sbjct: 57  IDLSVGTVAAMSSVVAALASAHGGWVAVVAG---CAAGLAVGVLNGVIITRLKILPFIVT 113

Query: 121 LAGMFFLRGVSYLVSEESIPINHPIYDTLSSLAWKIPGGGRLSAM---GLLMLAVVVIGI 177
           LA      GV+ L+ +             S   +   G G L  +   G++   V V G 
Sbjct: 114 LATSLGAHGVALLLGKNDA------VSIASDSNFANFGQGDLFGLPIPGIVAALVAVAGW 167

Query: 178 FLAHRTRFGNQVYAIGGNATSANLMGISTRSTTIRIYMLSTGLATLAGIVFSIYTQAGYA 237
                TRFG    AIGG+  +A LMG++   T +  Y +S  LA +AG++ +    AG  
Sbjct: 168 LALRSTRFGRHSLAIGGSEEAARLMGLNVDRTLVMAYAVSGLLAGMAGVILAAQFGAGQP 227

Query: 238 LAGVGVELDAIASVVIGGTLLSGGVGTVLGTLFGVAIQGLIQTYINFDG-----TLSSWW 292
             GVG EL AI++VV+GGTLL+GG G++  T+ GV + GL+   +NF+      +LS++W
Sbjct: 228 NEGVGWELFAISAVVLGGTLLTGGEGSIAMTIAGVLLLGLVFNLLNFENGLGFISLSAYW 287

Query: 293 TKIAIGILLFIFIALQ 308
             +  G+ L + I LQ
Sbjct: 288 QSVIRGVFLLLVIVLQ 303


Lambda     K      H
   0.329    0.145    0.428 

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: 309
Number of extensions: 20
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: 331
Length of database: 321
Length adjustment: 28
Effective length of query: 303
Effective length of database: 293
Effective search space:    88779
Effective search space used:    88779
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 (21.8 bits)
S2: 48 (23.1 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