GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natF in Azospirillum brasilense Sp245

Align Extracellular solute-binding protein, family 3 (characterized, see rationale)
to candidate AZOBR_RS08655 AZOBR_RS08655 amino acid ABC transporter substrate-binding protein

Query= uniprot:Q31RP1
         (359 letters)



>FitnessBrowser__azobra:AZOBR_RS08655
          Length = 340

 Score =  339 bits (870), Expect = 6e-98
 Identities = 169/321 (52%), Positives = 220/321 (68%), Gaps = 3/321 (0%)

Query: 40  ESNSRLNQVQARGKLLCGVEGRLPGFSFLDSQGNYSGLDVDICKAIAAALFNDPKAIEYR 99
           ++   L+ V+ RG + CGV   LPGF   DS GN++GLDVD C+A+A ALFNDP  +++ 
Sbjct: 22  QAGPTLDAVKGRGFVQCGVNAGLPGFGNPDSSGNWTGLDVDYCRAVAVALFNDPNKVKFT 81

Query: 100 SLDSVERFPALASGEVDLLSRNTTWTLSRDAKGGNNLEFAPTTFYDGQGLMVRRNSGIQS 159
            L + +RFPA+ SGEVDLLSRNTT TL+RD   G  L FAP T+YDGQG MV +  G++S
Sbjct: 82  PLSAQQRFPAIQSGEVDLLSRNTTVTLTRDTSVG--LNFAPVTYYDGQGFMVNKKLGVKS 139

Query: 160 LQDFQGKSICVETGTTSELNLADTMRELGVQYQEIKFPNSDANYAAYAQGRCEGVTSDRS 219
            ++  G ++CV+ GTT+ELNLAD  R   + Y  +   ++D   AAY  GRC+ +T+D S
Sbjct: 140 AKELNGATVCVQAGTTTELNLADYFRTNNMSYNPVVIESNDEVNAAYFAGRCDVLTTDAS 199

Query: 220 QLAARRTTLSDA-DQHQLLDAVISKEPLSPATLNNDSPWFDVVKWVVNATIQAEEFGITQ 278
            LA  R  ++   D H +L  +ISKEPL+PA  + D  WFDVVKW V ATIQAEE GIT 
Sbjct: 200 GLAGTRAGVAPVPDDHIILPEIISKEPLAPAVRHGDDQWFDVVKWTVYATIQAEEMGITS 259

Query: 279 ANIDQFKTSKNPEIRRFLGLEGELGQQLGLSNDFAYRAIKAVGNYGEIYERNVGQQSPLK 338
            N+D+F  SKNPEI+R LG    +G+ LGL   +AY  IK +GNYGEI+ERNVG ++PLK
Sbjct: 260 KNVDEFVNSKNPEIQRILGTSPGMGKALGLDEKWAYNIIKTMGNYGEIFERNVGTKTPLK 319

Query: 339 LNRGLNQLYKNGGLLYSPPFR 359
           L RGLN L+ NGGL Y+ P R
Sbjct: 320 LERGLNALWTNGGLQYAMPIR 340


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: 361
Number of extensions: 12
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: 340
Length adjustment: 29
Effective length of query: 330
Effective length of database: 311
Effective search space:   102630
Effective search space used:   102630
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