GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoxyribonate-transport in Rhizobium leguminosarum 3841

Align 2-deoxy-D-ribonate transporter 1 (characterized)
to candidate WP_049778410.1 RL_RS05180 MFS transporter

Query= reanno::WCS417:GFF1429
         (438 letters)



>NCBI__GCF_000009265.1:WP_049778410.1
          Length = 445

 Score =  310 bits (793), Expect = 8e-89
 Identities = 167/413 (40%), Positives = 251/413 (60%), Gaps = 7/413 (1%)

Query: 11  QALNKLMFVKLMPLLIIAYILSFLDRTNIALAKHHLDVDLGISAAAYGLGAGLFFLTYAL 70
           + L K+ F +++P +++ Y ++FLDR NI  A   ++ DLG S+  +G+GAG+FF+ Y L
Sbjct: 21  RVLRKITF-RIVPFIMLLYFIAFLDRVNIGFAALTMNQDLGFSSTVFGIGAGIFFVGYFL 79

Query: 71  SEIPSNLIMHKVGARFWIARIMVTWGLISAAMAFVQGETSFYVLRLLLGIAEAGLFPGVM 130
            E+PSNLI++KVGAR WIAR+M+TWG++S  MAFVQG TSFY LR LLG+AEAG FPG++
Sbjct: 80  FEVPSNLILNKVGARIWIARVMITWGIVSGLMAFVQGTTSFYALRFLLGVAEAGFFPGII 139

Query: 131 LYLTYWFNREQRARATGYFLLGVCFANIIGGPVGAALMRMDGMLGWHGWQWMFMLEGLPA 190
           LYL++WF   +RA  T  F+     + ++G P+  ALM M G LG  GWQWMF++E  PA
Sbjct: 140 LYLSFWFPARRRAAVTAIFMAAAPLSTVLGSPISGALMEMHGFLGLAGWQWMFLIEAAPA 199

Query: 191 VAFAWVVWRKLPDRPSKAPWLSAEEARGIEQRIAQETEEGAGEGGHSLKNWLTP-QILLA 249
           +    VV   L DRP KA WL+ EE   + + +  E + G  +  HS+   L   +++  
Sbjct: 200 IILGVVVLFYLTDRPEKAKWLTDEERSWLVKTMNAE-QAGKSKASHSILAGLADIRVIAL 258

Query: 250 IFVYFCHQITIYTVIFFLPSIISKYGELSTMSVGLLTSLPWIAAALGALLIPRFATTPGR 309
             VYF     +YT+  + P II ++G LS + VG + ++P I A +  +L  R +   G 
Sbjct: 259 ALVYFGTSAGLYTLGIWAPQIIKQFG-LSALQVGFINAIPGIFAVVAMILWARHSDKTGE 317

Query: 310 CRRLLVTGLLTMALGLGIASVSGPVFSLLGFCLSAVMFFVVQS--IIFLYPASRLKGVAL 367
               +V   L  A GL  A+ +  V+++L   L+ V   +  S   ++  P   L G A 
Sbjct: 318 RTWHVVGACLLAAAGLAFATGATSVYTVL-IALTLVNIGISSSKPPLWSMPTLFLSGPAA 376

Query: 368 AGGLGFVNACGLLGGFVGPSVMGVIEQSTGNAMNGLKVIALVLVVAALAALRL 420
           A G+  +N+ G LGGFVGPS++G I+ +TG+   GL  +A +L+++A+  L L
Sbjct: 377 AAGIATINSIGNLGGFVGPSMIGWIKDTTGSFAGGLYFVAGLLMISAILTLVL 429


Lambda     K      H
   0.327    0.141    0.438 

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: 549
Number of extensions: 26
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: 438
Length of database: 445
Length adjustment: 32
Effective length of query: 406
Effective length of database: 413
Effective search space:   167678
Effective search space used:   167678
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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