GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HP1174 in Dyella japonica UNC79MFTsu3.2

Align Glucose/galactose porter (characterized)
to candidate N515DRAFT_0592 N515DRAFT_0592 glucose/galactose transporter

Query= TCDB::P0C105
         (412 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0592
          Length = 430

 Score =  207 bits (528), Expect = 4e-58
 Identities = 137/403 (33%), Positives = 208/403 (51%), Gaps = 25/403 (6%)

Query: 30  LLFFMWGFITCLNDILIPHLKNVFQLNYTQSMLIQFCFFGAYFIVSLPAGQLVKRISYKR 89
           LLFF++GF+T LN  LI  +K  F L+   + L+   F+ +YF ++LP+  ++KR   K+
Sbjct: 26  LLFFIFGFVTWLNGPLITFVKLAFSLDDVNAFLVPMVFYCSYFFLALPSSAVLKRTGMKK 85

Query: 90  GIVVGLIVAAIGCALFIPAASYRVYALFLGALFVLASGVTILQVAANPYVTILGKPETAA 149
           G+ +GL V AIG  LF    S RVY   L  LFV+ +G+ +LQ A+NPY++ILG  ++AA
Sbjct: 86  GMALGLFVMAIGAVLFGQFVSMRVYGGALAGLFVIGAGLALLQTASNPYISILGPIDSAA 145

Query: 150 SRLTLTQAFNSLGTTVAPVFGAVLILSA---------------ATDATVNAEADAVRFPY 194
            R+      N +   +AP     L+LS                A +A +N  A  V  PY
Sbjct: 146 QRIAFMGICNKVAGALAPFVFGWLVLSGIDTFDQQVKAAPTPEAREALLNTFAAKVHMPY 205

Query: 195 LLLALAFTVLAIIFAILKPPDVQ---EDEPALSDKKEGSAWQYRHLVLGAIGIFVYVGAE 251
           L +A    +LA+       P+++    +  A     +G+   + HL LG + +F+YVG E
Sbjct: 206 LAMAGLLVLLAVWVLRSPLPEIKPSGANSEAEIGHAKGNLLSFPHLWLGVLCLFLYVGVE 265

Query: 252 VSVGSFLVNFLSDPTVAGLSETDAAHHVAYFWGGAMVGRFIGSAAM--RYIDDGKALAFN 309
           V  G  +  +       GL   DA  H   F   AM+  ++    +  + I     LA +
Sbjct: 266 VMAGDAIGTYGQG---LGL-PLDATKHFTSFTLFAMLLGYLAGLVLIPKIISQQSYLAVS 321

Query: 310 AFVAIILLFITVATTGHIAMWSVLAIGLFNSIMFPTIFSLALHGLGSHTSQGSGILCLAI 369
           A + +       ATTG+ ++  V A+G  N++M+P IF LA+ GLG  T  GS +L +AI
Sbjct: 322 AVLGVAFTVGAWATTGYTSVGFVAALGFANAMMWPAIFPLAIKGLGRWTEAGSALLIMAI 381

Query: 370 VGGAIVPLIQGALADAIGIHLAFLMPII-CYAYIAFYGLIGSK 411
           VGGA+VP     L       L F++ ++ CY YI FYGL G +
Sbjct: 382 VGGALVPQAFVHLKQHYDFQLVFMLLMVPCYLYILFYGLRGHR 424


Lambda     K      H
   0.328    0.141    0.420 

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: 543
Number of extensions: 42
Number of successful extensions: 5
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: 412
Length of database: 430
Length adjustment: 32
Effective length of query: 380
Effective length of database: 398
Effective search space:   151240
Effective search space used:   151240
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