GapMind for catabolism of small carbon sources

 

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

Align Xanthosine permease; Xanthosine transporter (characterized)
to candidate N515DRAFT_2002 N515DRAFT_2002 MFS transporter, NHS family, xanthosine permease

Query= SwissProt::P45562
         (418 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2002
          Length = 420

 Score =  471 bits (1212), Expect = e-137
 Identities = 232/412 (56%), Positives = 303/412 (73%), Gaps = 4/412 (0%)

Query: 1   MSIAMRLKVMSFLQYFIWGSWLVTLGSYMINTLHFTGANVGMVYSSKGIAAIIMPGIMGI 60
           MSI +RL +M FLQYF+WGSWL+T+G+Y     H+ G   G ++S+ GIA++ MP I G+
Sbjct: 1   MSIKLRLVIMYFLQYFVWGSWLLTIGAYWFQNKHWPGTQFGAIFSTMGIASLFMPSIAGV 60

Query: 61  IADKWLRAERAYMLCHLVCAGVLFYAASVTDPDMMFWVMLVNAMAFMPTIALSNSVSYSC 120
           IADKW+ AE+   L H+  A +LF   ++  P +MFWVML+N M +MPTI+LS +V+Y+ 
Sbjct: 61  IADKWINAEKLLGLMHIGGAIMLFVVPAIDSPGLMFWVMLLNMMFYMPTISLSIAVAYNA 120

Query: 121 LAQAGLDPVTAFPPIRVFGTVGFIVAMWAVSLLHLELSSLQLYIASGASLLLSAYALTLP 180
           L  +G D VT FPPIRV+GTVGFI A+W VSLLHLE ++ Q ++A  A+LLL  YA TLP
Sbjct: 121 LKSSGEDIVTVFPPIRVWGTVGFIAALWTVSLLHLETTAGQFHVAGAAALLLGLYAFTLP 180

Query: 181 KIPVA-EKKATTSLASKLGLDAFVLFKNPRMAIFFLFAMMLGAVLQITNVFGNPFLHDFA 239
           K P   E+K   SL   LGL +F L +N +MAIFF+FAM+LGA LQ+TN +G+ FLHDFA
Sbjct: 181 KCPPRFERKEQQSLLDTLGLTSFALLRNTQMAIFFMFAMLLGAALQLTNAYGDTFLHDFA 240

Query: 240 RNPEFADSFVVKYPSILLSVSQMAEVGFILTIPFFLKRFGIKTVMLMSMVAWTLRFGFFA 299
               + +   V+YP+I++S+SQ++E  FIL IPFFLKRFGIKTVML+SM+AWTLRFG FA
Sbjct: 241 AMEPYKNLIAVRYPAIIMSISQISETLFILAIPFFLKRFGIKTVMLISMLAWTLRFGLFA 300

Query: 300 YGDPSTTGFILLLLSMIVYGCAFDFFNISGSVFVEQEVDSSIRASAQGLFMTMVNGVGAW 359
           YGDP   G  +++LS IVYG AFDFFNISGS+FVE + D SIRASAQGLFM M NG+GA 
Sbjct: 301 YGDPG-AGLWMIVLSCIVYGMAFDFFNISGSLFVEGQADPSIRASAQGLFMLMTNGIGAV 359

Query: 360 VGSILSGMAVDYF--SVDGVKDWQTIWLVFAGYALFLAVIFFFGFKYNHDPE 409
           +GS +SG  +D F    DG K+W  IW+ F+ Y+L +AV+F F FK+ HDP+
Sbjct: 360 LGSSVSGWMIDAFFTQADGSKNWHGIWITFSLYSLIVAVLFVFLFKHKHDPK 411


Lambda     K      H
   0.330    0.141    0.435 

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: 567
Number of extensions: 33
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: 418
Length of database: 420
Length adjustment: 32
Effective length of query: 386
Effective length of database: 388
Effective search space:   149768
Effective search space used:   149768
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 (21.9 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