GapMind for catabolism of small carbon sources

 

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

Align Na+/H+ dicarboxylate symporter (characterized, see rationale)
to candidate N515DRAFT_1080 N515DRAFT_1080 Na+/H+-dicarboxylate symporter

Query= uniprot:L0GT47
         (419 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1080
          Length = 422

 Score =  308 bits (788), Expect = 3e-88
 Identities = 161/397 (40%), Positives = 244/397 (61%), Gaps = 4/397 (1%)

Query: 20  WQQILIGLALGVAAGMAFG-ADAQLLAPIGTLFLNAIKMLIVPLVFVSLVAGITSMQDSA 78
           W+++L G  LG  AG   G        P+G +++  IKM+ VPLVF ++V  ++S+    
Sbjct: 13  WKRVLAGFVLGALAGWLCGPGSVAWFQPLGDVYVALIKMIAVPLVFFAVVNSVSSLHGVQ 72

Query: 79  KLGRISLKTIAIYLVTTAFAVSIGLLFGALFSPGEGMNMVA-SGNEQAKQAPSLVSILVG 137
           ++  +  +T   + +T A AV +GLL G L  PG G+  +  +G+ + ++ PS V +L+ 
Sbjct: 73  RMAALGGRTFLWFALTAALAVGVGLLVGHLTDPGLGVGQLTMAGDYKVREVPSAVKVLLD 132

Query: 138 LVPANPVTAFAEGNILQIIVFAIALGVSINLIGERGAPAVRLFDALAETFYKLTDLVMRV 197
           +VP NP  A +EG ILQ+I FA  LG+++  IGE+ A    LF    +   ++T  V+ +
Sbjct: 133 VVPTNPFRALSEGKILQVIFFAGLLGLALVKIGEKSARLRELFGEANDAMIQVTRFVLEM 192

Query: 198 APIGVFALTAGVVGSHGAEVLLPLAGVIGVIYLASIAHVLLVYGGLLGLLARLNPLRFFQ 257
            PIG F L A +V  +G E LLPL   +  +Y A    +++VYGGLL L   L+P RFF+
Sbjct: 193 TPIGTFGLIAALVAGYGFEKLLPLGKFVLALYAACAVQIVVVYGGLL-LAHGLSPRRFFR 251

Query: 258 GIAPALAVAFSTSSSSGTLPVSIECARKNLGVSEGVAGFVLPVGATINMDGT-AIYQGVL 316
           G+ PA+ VAF++SSS  ++PV++    +NLGVS   A F +P+GA+I MDG  AIY  + 
Sbjct: 252 GVLPAMQVAFTSSSSFASMPVALRSVTQNLGVSPAYASFAVPLGASIKMDGCGAIYPAIS 311

Query: 317 ALFIAQAFGIDLSAGQYAMIILTATLASIGTAGIPGAGLIMLGLVLTAAGLPLEGVALIA 376
           ++F+AQ FG+ L   QY +I+L + L S GTAG+PG   +M+ LVL++AGLP+EG+  + 
Sbjct: 312 SIFVAQYFGLQLEPAQYFVILLASVLGSFGTAGVPGTATVMVTLVLSSAGLPVEGIGYLV 371

Query: 377 GIDRILDMARTTVNVAGDLMTTTLVGRSEQELDRAIY 413
            IDR+LDM RT  NV G ++   LV R +  LD  +Y
Sbjct: 372 AIDRVLDMMRTMTNVTGQMLVPVLVAREQGLLDMDVY 408


Lambda     K      H
   0.324    0.140    0.386 

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: 550
Number of extensions: 36
Number of successful extensions: 4
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: 419
Length of database: 422
Length adjustment: 32
Effective length of query: 387
Effective length of database: 390
Effective search space:   150930
Effective search space used:   150930
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 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