GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdcC in Pseudomonas fluorescens GW456-L13

Align Threonine/serine transporter TdcC; H(+)/threonine-serine symporter (characterized)
to candidate PfGW456L13_3379 Serine transporter

Query= SwissProt::P0AAD8
         (443 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3379
          Length = 396

 Score =  386 bits (991), Expect = e-112
 Identities = 201/417 (48%), Positives = 278/417 (66%), Gaps = 24/417 (5%)

Query: 26  LGLFGTAIGAGVLFFPIRAGFGGLIPILLMLVLAYPIAFYCHRALARLCLSGSNPSGNIT 85
           LGLFGTAIGAG LF PI AG GG  P+L++ +LA+P+ FY HR L R  LSG     +IT
Sbjct: 2   LGLFGTAIGAGTLFLPINAGLGGFWPLLILALLAFPMTFYAHRGLTRFVLSGRE-GADIT 60

Query: 86  ETVEEHFGKTGGVVITFLYFFAICPLLWIYGVTITNTFMTFWENQLGFAPLNRGFVALFL 145
           E VEEHFG   G +IT LYFFAI P+L IY V +TNT  +F E+QL   P  R  ++L L
Sbjct: 61  EVVEEHFGIKAGALITLLYFFAIFPILLIYSVALTNTVGSFLEHQLHITPPPRAVLSLVL 120

Query: 146 LLLMAFVIWFGKDLMVKVMSYLVWPFIASLVLISLSLIPYWNSAVIDQVDLGSLSLTGHD 205
           +L +  V+  G+ ++VK MS +V+PFI +L+ +++ LIP+WN  ++         +    
Sbjct: 121 ILGLLAVVRCGEQMIVKAMSLMVYPFIVALLFLAVYLIPHWNGGILATAS----QVPAPS 176

Query: 206 GILITVWLGISIMVFSFNFSPIVSSFVVSKREEYEKDFGRDFTERKCSQIISRASMLMVA 265
            +L T+WL I +MVFSFN SPI+S+F V ++  Y      +  E + SQI+SRA +LMV 
Sbjct: 177 ALLHTLWLAIPVMVFSFNHSPIISAFAVDQKRRY-----GEHAEERSSQILSRAHLLMVV 231

Query: 266 VVMFFAFSCLFTLSPANMAEAKAQNIPVLSYLANHFASMTGTKTTFAITLEYAASIIALV 325
           +V+FF FSC+ TLSPA +AEAKAQN+ +LSYLANHF++          T+ +AA +IA V
Sbjct: 232 MVLFFVFSCVLTLSPAQLAEAKAQNLSILSYLANHFSNP---------TIAFAAPLIAFV 282

Query: 326 AIFKSFFGHYLGTLEGLNGLVLKFGYKGDKTKVSLGKLNTISMIFIMGSTWVVAYANPNI 385
           AI KSF GHY+G  EGL GL++K G      + S   L+ ++  F++   W+VA  NP+I
Sbjct: 283 AISKSFLGHYIGASEGLKGLIVKSG-----KRPSAKALDRMTAAFMLVVCWIVATLNPSI 337

Query: 386 LDLIEAMGAPIIASLLCLLPMYAIRKAPSLAKYRGRLDNVFVTVIGLLTILNIVYKL 442
           L +IE +G P+IA++L L+PMYAIRK P++A+YRG+  NVFVT +GL+ I  +VY L
Sbjct: 338 LGMIETLGGPVIAAILFLMPMYAIRKVPAMARYRGQASNVFVTAVGLVAISALVYSL 394


Lambda     K      H
   0.328    0.141    0.430 

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: 482
Number of extensions: 27
Number of successful extensions: 7
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: 443
Length of database: 396
Length adjustment: 32
Effective length of query: 411
Effective length of database: 364
Effective search space:   149604
Effective search space used:   149604
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 (21.8 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