GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TAT in Escherichia coli BW25113

Align tryptophan permease (characterized)
to candidate 16265 b2156 lysine transporter (NCBI)

Query= CharProtDB::CH_091156
         (592 letters)



>FitnessBrowser__Keio:16265
          Length = 489

 Score =  273 bits (699), Expect = 9e-78
 Identities = 151/429 (35%), Positives = 237/429 (55%), Gaps = 5/429 (1%)

Query: 74  DTSNLKRTLKPRHLIMIAIGGSIGTGLFVGSGKAIAEGGPLGVVIGWAIAGSQIIGTIHG 133
           +   L+R LK RHL MIAIGGSIGTGLFV SG  I++ GP G ++ + + G  +   +  
Sbjct: 9   EAPGLRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYMLIGLMVYFLMTS 68

Query: 134 LGEITVRFPVVGAFANYGTRFLDPSISFVVSTIYVLQWFFVLPLEIIAAAMTVQYWNSSI 193
           LGE+    PV G+FA YG  +++    F +   Y   W   + ++++AA + + +W    
Sbjct: 69  LGELAAYMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQLVMSWWFPDT 128

Query: 194 DPVIWVAIFYAVIVSINLFGVRGFGEAEFAFSTIKAITVCGFIILCVVLICGGGPDHEFI 253
              IW A+F  VI  +N   VRGFGEAE+ FS IK  TV  FII+ V++I G     +  
Sbjct: 129 PGWIWSALFLGVIFLLNYISVRGFGEAEYWFSLIKVTTVIVFIIVGVLMIIGIFKGAQPA 188

Query: 254 GAKYWH-DPGCLANGFPGVLSVLVVASYSLGGIEMTCLASGET-DP-KGLPSAIKQVFWR 310
           G   W       A GF  ++ V ++  +S  G E+  +A+GE+ DP K +P A++QVFWR
Sbjct: 189 GWSNWTIGEAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESEDPAKNIPRAVRQVFWR 248

Query: 311 ILFFFLISLTLVGFLVPYTNQNLLGG--SSVDNSPFVIAIKLHHIKALPSIVNAVILISV 368
           IL F++ ++ ++  ++PYT+ +LL      +  SPF +  +   + +  +++NAVIL +V
Sbjct: 249 ILLFYVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSAAAVMNAVILTAV 308

Query: 369 LSVGNSCIFASSRTLCSMAHQGLIPWWFGYIDRAGRPLVGIMANSLFGLLAFLVKSGSMS 428
           LS GNS ++AS+R L ++A  G  P  F  + R G P   + A ++   L FL       
Sbjct: 309 LSAGNSGMYASTRMLYTLACDGKAPRIFAKLSRGGVPRNALYATTVIAGLCFLTSMFGNQ 368

Query: 429 EVFNWLMAIAGLATCIVWLSINLSHIRFRLAMKAQGKSLDELEFVSAVGIWGSAYSALIN 488
            V+ WL+  +G+   I WL I +SH RFR     QG  +++L + S     G  ++ ++ 
Sbjct: 369 TVYLWLLNTSGMTGFIAWLGIAISHYRFRRGYVLQGHDINDLPYRSGFFPLGPIFAFILC 428

Query: 489 CLILIAQFY 497
            +I + Q Y
Sbjct: 429 LIITLGQNY 437


Lambda     K      H
   0.326    0.141    0.447 

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: 792
Number of extensions: 44
Number of successful extensions: 5
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: 592
Length of database: 489
Length adjustment: 35
Effective length of query: 557
Effective length of database: 454
Effective search space:   252878
Effective search space used:   252878
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 (21.6 bits)
S2: 52 (24.6 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