GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdcC in Escherichia coli BW25113

Align Threonine/serine transporter TdcC; H(+)/threonine-serine symporter (characterized)
to candidate 16926 b2845 predicted transporter (NCBI)

Query= SwissProt::P0AAD8
         (443 letters)



>FitnessBrowser__Keio:16926
          Length = 409

 Score =  222 bits (566), Expect = 1e-62
 Identities = 130/420 (30%), Positives = 227/420 (54%), Gaps = 22/420 (5%)

Query: 17  WRKSDTTWTLGLFGTAIGAGVLFFPIRAGFGGLIPILLMLVLAYPIAFYCHRALARLCLS 76
           W K +T W+  L+GTA+GAG LF PI+ G  G + + +  ++A+P+ ++ H+AL +  LS
Sbjct: 5   WSKEETLWSFALYGTAVGAGTLFLPIQLGSAGAVVLFITALVAWPLTYWPHKALCQFILS 64

Query: 77  GSNPSG-NITETVEEHFGKTGGVVITFLYFFAICPLLWIYGVTITNTFMTFWENQLGFAP 135
               +G  IT  V  ++GK  G +IT LYF A   ++ IY V ITN+        +    
Sbjct: 65  SKTSAGEGITGAVTHYYGKKIGNLITTLYFIAFFVVVLIYAVAITNSLTEQLAKHMVIDL 124

Query: 136 LNRGFVALFLLLLMAFVIWFGKDLMVKVMSYLVWPFIASLVLISLSLIPYWNSAVIDQVD 195
             R  V+L ++L++  +   G+   ++VM +LV+P IA  + +S+ L+  W      Q D
Sbjct: 125 RIRMLVSLGVVLILNLIFLMGRHATIRVMGFLVFPLIAYFLFLSIYLVGSW------QPD 178

Query: 196 LGSLSLTGHDGILITVWLGISIMVFSFNFSPIVSSFVVSKREEYEKDFGRDFTERKCSQI 255
           L +  +  +   L  +W+ I +MVF+F+ +PI+S+F + +RE+Y      +    KC +I
Sbjct: 179 LLTTQVEFNQNTLHQIWISIPVMVFAFSHTPIISTFAIDRREKY-----GEHAMDKCKKI 233

Query: 256 ISRASMLMVAVVMFFAFSCLFTLSPANMAEAKAQNIPVLSYLANHFASMTGTKTTFAITL 315
           +  A +++   V+FF FSCL ++ P+ +  AK + + +LS L     SM      +   L
Sbjct: 234 MKVAYLIICISVLFFVFSCLLSIPPSYIEAAKEEGVTILSAL-----SMLPNAPAW---L 285

Query: 316 EYAASIIALVAIFKSFFGHYLGTLEGLNGLVLKFGYKGDKTKVSLGKLNTISMIFIMGST 375
             +  I+A+VA+ KSF G Y G +EG    V+K   +    K S      +S++ +   T
Sbjct: 286 SISGIIVAVVAMSKSFLGTYFGVIEGATE-VVKTTLQQVGVKKSRAFNRALSIMLVSLIT 344

Query: 376 WVVAYANPNILDLIEAMGAPIIASLLCLLPMYAIRKAPSLAKYRGRLDNVFVTVIGLLTI 435
           ++V   NPN + +I A+  P+IA +L ++P  +    P+L  +R  + N+   ++G+L +
Sbjct: 345 FIVCCINPNAISMIYAISGPLIAMILFIMPTLSTYLIPALKPWRS-IGNLITLIVGILCV 403


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: 519
Number of extensions: 26
Number of successful extensions: 8
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: 409
Length adjustment: 32
Effective length of query: 411
Effective length of database: 377
Effective search space:   154947
Effective search space used:   154947
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: 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