GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manP in Escherichia coli BW25113

Align protein-Npi-phosphohistidine-D-mannose phosphotransferase (EC 2.7.1.191) (characterized)
to candidate 17988 b3949 predicted enzyme IIC component of PTS (NCBI)

Query= BRENDA::O31645
         (650 letters)



>FitnessBrowser__Keio:17988
          Length = 359

 Score =  285 bits (729), Expect = 2e-81
 Identities = 157/337 (46%), Positives = 217/337 (64%), Gaps = 17/337 (5%)

Query: 125 RHLMNGVSFMVPFIVVGGLLIAVALTLGGEKTPKGLVIPD---DSFWKTIEQIGSASFSF 181
           +HLM GVS M+PF+V GG+L+AV++ L G    KG V PD   D   K +  IG A  + 
Sbjct: 13  QHLMTGVSHMIPFVVSGGILLAVSVMLYG----KGAV-PDAVADPNLKKLFDIGVAGLTL 67

Query: 182 MIPILAGYIAYSIADKPGLVPGMIGGYIAATGSFYDSASGAGFLGGIIAGFLAGYAALWI 241
           M+P LA YI YSIA++  L P  IG ++        ++ GAGF G +IAG + G    ++
Sbjct: 68  MVPFLAAYIGYSIAERSALAPCAIGAWVG-------NSFGAGFFGALIAGIIGGIVVHYL 120

Query: 242 KKLKVPKAIQPIMPIIIIPVFASLIVGLAFVFLIGAPVAQIFASLTVWLAGMKGSSSILL 301
           KK+ V K ++ +MPI IIP+  +LI     ++ +G PV  +  SLT WL GM+  S ++L
Sbjct: 121 KKIPVHKVLRSVMPIFIIPIVGTLITAGIMMWGLGEPVGALTNSLTQWLQGMQQGSIVML 180

Query: 302 ALILGAMISFDMGGPVNKVAFLFGSAMIGEGNYEIMGPIAVAICIPPIGLGIATFLGKRK 361
           A+I+G M++FDMGGPVNKVA+ F    + +G Y ++   AV ICIPP+G+G+AT +G++ 
Sbjct: 181 AVIMGLMLAFDMGGPVNKVAYAFMLICVAQGVYTVVAIAAVGICIPPLGMGLATLIGRKN 240

Query: 362 FEASQREMGKAAFTMGLFGITEGAIPFAAQDPLRVIPSIMAGSMTGSVIAMIGNVGDRVA 421
           F A +RE GKAA  MG  G+TEGAIPFAA DPLRVIPSIM GS+ G+V A +  VG +  
Sbjct: 241 FSAEERETGKAALVMGCVGVTEGAIPFAAADPLRVIPSIMVGSVCGAVTAAL--VGAQCY 298

Query: 422 HGGPIVAVLGAVDHVLMFFIAVIAGSLVTALFVNVLK 458
            G   + VL  V+  L +  AV  G++VTA+ VNVLK
Sbjct: 299 AGWGGLIVLPVVEGKLGYIAAVAVGAVVTAVCVNVLK 335


Lambda     K      H
   0.319    0.137    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: 569
Number of extensions: 31
Number of successful extensions: 6
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: 650
Length of database: 359
Length adjustment: 34
Effective length of query: 616
Effective length of database: 325
Effective search space:   200200
Effective search space used:   200200
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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