GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malF_Aa in Escherichia coli BW25113

Align Binding-protein-dependent transport systems inner membrane component (characterized, see rationale)
to candidate 18061 b4033 maltose transporter subunit (NCBI)

Query= uniprot:C8WUR0
         (321 letters)



>FitnessBrowser__Keio:18061
          Length = 514

 Score =  181 bits (460), Expect = 3e-50
 Identities = 97/252 (38%), Positives = 152/252 (60%), Gaps = 6/252 (2%)

Query: 66  GLKNYEELLNPHDPLSNLFLPTFIWTLVYALCTTALAYLVGLFLAVLLNNKHMRERTLYR 125
           G KN+  +    + +   FL  F+WT+V++L T  L   VG+ LA L+  + +R + +YR
Sbjct: 260 GWKNFTRVFTD-EGIQKPFLAIFVWTVVFSLITVFLTVAVGMVLACLVQWEALRGKAVYR 318

Query: 126 TLLIVPWAVPNLISMLAWQGLLNDQYGQINALLHGVFGLPRIPWLTSALWARIAVIMVNV 185
            LLI+P+AVP+ IS+L ++GL N  +G+IN +L  +FG+ +  W +    AR  +I+VN 
Sbjct: 319 VLLILPYAVPSFISILIFKGLFNQSFGEINMMLSALFGV-KPAWFSDPTTARTMLIIVNT 377

Query: 186 WAGFPYMMTVCLGALQSIPTDQYEAAEIDGANWWQVFRYVTMPSVWRISLPLLIPSFSYN 245
           W G+PYMM +C+G L++IP D YEA+ +DGA  +Q F  +T+P + +   PL+I SF++N
Sbjct: 378 WLGYPYMMILCMGLLKAIPDDLYEASAMDGAGPFQNFFKITLPLLIKPLTPLMIASFAFN 437

Query: 246 FNNFNASYLLTGGGPPN-SNNPFLGQTDILATAAYKMTLT---FNRYDLGATISVLLFIL 301
           FNNF    LLT GGP         G TD+L    Y++         + L A I+ L+F+L
Sbjct: 438 FNNFVLIQLLTNGGPDRLGTTTPAGYTDLLVNYTYRIAFEGGGGQDFGLAAAIATLIFLL 497

Query: 302 VALISWVQMRYT 313
           V  ++ V ++ T
Sbjct: 498 VGALAIVNLKAT 509



 Score = 28.5 bits (62), Expect = 4e-04
 Identities = 11/40 (27%), Positives = 25/40 (62%)

Query: 24  AYGYLSPALVTICVLSILPIFYTIYISFTNFNQMHFLSYQ 63
           A+ Y+ P +  + +  + P+  TI I+FTN++  + L+++
Sbjct: 64  AWRYVYPGMAGMGLFVLFPLVCTIAIAFTNYSSTNQLTFE 103


Lambda     K      H
   0.327    0.140    0.451 

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: 457
Number of extensions: 29
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 321
Length of database: 514
Length adjustment: 31
Effective length of query: 290
Effective length of database: 483
Effective search space:   140070
Effective search space used:   140070
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 (21.7 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