GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gltP in Sphingomonas koreensis DSMZ 15582

Align Na+/H+ dicarboxylate symporter (characterized, see rationale)
to candidate Ga0059261_3350 Ga0059261_3350 Na+/H+-dicarboxylate symporters

Query= uniprot:L0GT47
         (419 letters)



>FitnessBrowser__Korea:Ga0059261_3350
          Length = 436

 Score =  308 bits (788), Expect = 3e-88
 Identities = 171/404 (42%), Positives = 241/404 (59%), Gaps = 5/404 (1%)

Query: 19  LWQQILIGLALGVAAGMAFGADAQLLAPIGTLFLNAIKMLIVPLVFVSLVAGITSMQDSA 78
           LW++IL  L LG  AG+A+G  A  +A IG LF+  I+ML+VPLVF+++ AG+ ++ D  
Sbjct: 31  LWRRILGALVLGAIAGVAWGPGATSIAWIGELFVRLIRMLVVPLVFLTIAAGVAALADPK 90

Query: 79  KLGRISLKTIAIYLVTTAFAVSIGLLFGALFSPGEGMNMVASGNEQAKQAPSLVSILVGL 138
           +LG I +KT+A+Y+ TT  AV+ GL+   L  PG G +   +        P    + + +
Sbjct: 91  RLGSIGVKTLAMYVFTTTLAVTTGLIVATLIGPGIGASFADAVPRAMGTPPDTARMFMEI 150

Query: 139 VPANPVTAFAEGNILQIIVFAIALGVSINLIGERGAPAVRLFDALAETFYKLTDLVMRVA 198
           +P NPV A A+G  L +I FAI +G  +   G+   P     +  ++   K+   VM  A
Sbjct: 151 IPDNPVGAMADGKTLSVIFFAILVGAGVIAAGKGAEPVRAFLNGASDVMLKIVGFVMETA 210

Query: 199 PIGVFALTAGVVGSHGAEVLLPLAGVIGVIYLASIAHVLLVYGGL-LGLLARLNPLRFFQ 257
           P GVFAL A V+G+ G    L +  +   +   S    LL++G + + L+A L+PL FF+
Sbjct: 211 PFGVFALIAVVMGTSGPASFLAILKLAICVVAGSAVVTLLIHGLIVVRLMAWLSPLPFFR 270

Query: 258 GIAPALAVAFSTSSSSGTLPVSIECARKNLGVSEGVAGFVLPVGATINMDGTAIYQGVLA 317
           GIA A+ V FSTSSSS TLPV+I  A+ NLG+S+ VA  VLP+GATI MDG A+Y  +L 
Sbjct: 271 GIADAIMVGFSTSSSSATLPVAIRVAQNNLGISKPVASTVLPLGATIGMDGAAMYVAMLT 330

Query: 318 LFIAQAFGIDLSAGQYAMIILTATLASIGTAGIPGAGLIMLGLVLTAAGLPLEGVALIAG 377
           LF AQAFG+DL+   Y +I  T T+ ++G A +P   L +L  VL A G+  E  AL+ G
Sbjct: 331 LFSAQAFGLDLTWADYLVIAATTTIVAMGVAPVPSGSLFVLAAVLHAIGITPEQTALVVG 390

Query: 378 ----IDRILDMARTTVNVAGDLMTTTLVGRSEQELDRAIYDSSN 417
                DRILDM RT  NV  DL   T V R E E+D  +Y+S+N
Sbjct: 391 FVLPFDRILDMTRTVPNVTSDLAIATAVARWEGEMDVTVYNSAN 434


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: 574
Number of extensions: 35
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: 419
Length of database: 436
Length adjustment: 32
Effective length of query: 387
Effective length of database: 404
Effective search space:   156348
Effective search space used:   156348
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: 51 (24.3 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