GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natF in Dinoroseobacter shibae DFL-12

Align Extracellular solute-binding protein, family 3 (characterized, see rationale)
to candidate 3606888 Dshi_0318 cationic amino acid ABC transporter, periplasmic binding protein (RefSeq)

Query= uniprot:Q31RP1
         (359 letters)



>FitnessBrowser__Dino:3606888
          Length = 338

 Score =  299 bits (766), Expect = 6e-86
 Identities = 145/316 (45%), Positives = 201/316 (63%), Gaps = 3/316 (0%)

Query: 45  LNQVQARGKLLCGVEGRLPGFSFLDSQGNYSGLDVDICKAIAAALFNDPKAIEYRSLDSV 104
           L +VQARG + CG+   L GF+  D+ G + G DV +C+A+AAA+F DP A+ +  + + 
Sbjct: 25  LEEVQARGAVNCGISTGLVGFASQDANGEWQGFDVAVCRAVAAAVFGDPTAVNFNPVTNQ 84

Query: 105 ERFPALASGEVDLLSRNTTWTLSRDAKGGNNLEFAPTTFYDGQGLMVRRNSGIQSLQDFQ 164
            RF  L SGE+D+L+RNTTWT SRD      LEF    +YDGQG MV +  G+ S  +  
Sbjct: 85  VRFEVLNSGEIDMLARNTTWTFSRDVD--LKLEFTGINYYDGQGFMVPKALGVSSATELD 142

Query: 165 GKSICVETGTTSELNLADTMRELGVQYQEIKFPNSDANYAAYAQGRCEGVTSDRSQLAAR 224
           G ++C++ GTT+ELNLAD  R   + ++ +    +      Y  G C+  T+D S LAA 
Sbjct: 143 GATVCIQKGTTTELNLADFFRANNISFEPVPISTASEAQQQYLAGACDVYTTDASGLAAT 202

Query: 225 RTTLSDADQHQLLDAVISKEPLSPATLNNDSPWFDVVKWVVNATIQAEEFGITQANIDQF 284
           R +    D+H +L  +ISKEPL P   + D+ W D+V+W +NA I AEE G+T AN+ + 
Sbjct: 203 RASFESPDEHVVLPEIISKEPLGPLVRHGDNEWGDIVRWTLNALIAAEELGVTSANVAEL 262

Query: 285 KT-SKNPEIRRFLGLEGELGQQLGLSNDFAYRAIKAVGNYGEIYERNVGQQSPLKLNRGL 343
              + NPEI R LG EG LG+QLGLS D+A   IKA GNYGEI+E ++G+ +P+ L RGL
Sbjct: 263 AAGTDNPEINRLLGTEGNLGEQLGLSADWAVNVIKAGGNYGEIFETHIGENTPIGLARGL 322

Query: 344 NQLYKNGGLLYSPPFR 359
           N  +  GGLLY+PPFR
Sbjct: 323 NAQWTEGGLLYAPPFR 338


Lambda     K      H
   0.317    0.134    0.391 

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: 299
Number of extensions: 11
Number of successful extensions: 3
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: 359
Length of database: 338
Length adjustment: 29
Effective length of query: 330
Effective length of database: 309
Effective search space:   101970
Effective search space used:   101970
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 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