Aligments for a candidate for treF in Shewanella oneidensis MR-1

GapMind for catabolism of small carbon sources

Aligments for a candidate for treF in Shewanella oneidensis MR-1

Align Putative alpha-glucosidase AglA (characterized, see rationale)
to candidate 201365 SO2213 oligo-1,6-glucosidase (NCBI ptt file)

Query= uniprot:I7EUW4
         (552 letters)



>lcl|FitnessBrowser__MR1:201365 SO2213 oligo-1,6-glucosidase (NCBI
           ptt file)
          Length = 540

 Score =  569 bits (1467), Expect = e-167
 Identities = 267/500 (53%), Positives = 345/500 (69%), Gaps = 5/500 (1%)

Query: 19  WWRGAVIYQIYPRSYQDSNGDGIGDLRGITQRLPHIASLGVDAIWISPFFTSPMKDFGYD 78
           WWRGAVIYQIYPRS  D+NGDG+GDLRGI  +L +IASL VDAIWISPFF SPM DFGYD
Sbjct: 6   WWRGAVIYQIYPRSLLDTNGDGVGDLRGIITKLDYIASLNVDAIWISPFFKSPMADFGYD 65

Query: 79  VSDYCDVDPMFGSLSNFDQLVAAAHRLGLRVMIDLVLSHTSDQHAWFGESRQSRDNARAD 138
           +SDY ++DP+FGS+ +FD+L+  AH+ G++V+ID VLSHTSDQHAWF ESR+SR N +AD
Sbjct: 66  ISDYREIDPLFGSMQDFDELIEKAHQRGIKVIIDQVLSHTSDQHAWFIESRESRTNPKAD 125

Query: 139 WYVWADPQPDGTPPNNWLSIFGGSAWQWDPRREQYYLHNFLVSQPDLNFHSPAVQDALLD 198
           WYVWADP+ DGTPPNNWL+IFGG AW+W+PRR+QYYLHNFL SQPD+NFH+P V+ A+LD
Sbjct: 126 WYVWADPREDGTPPNNWLAIFGGCAWEWEPRRQQYYLHNFLRSQPDINFHNPDVRQAVLD 185

Query: 199 VTRFWLERGVDGFRLDTINFYYHDAELRSNPALPPEQRNATIAPSVNPYNHQEHLYSKNQ 258
              FWL++GVDGFRLD I F +HD  LR NPA P E+R        NPY +Q H Y+ ++
Sbjct: 186 NVEFWLKKGVDGFRLDAITFCFHDELLRDNPAKPKEKRQGRGFSEDNPYAYQYHYYNNDR 245

Query: 259 PENLAFLGRFRALLDEYPAKAAVGEVGDAQRGLEIMGSYTAANTGVHMCYAFELLAKDVL 318
           P+ + F+   R L++ YP    +GEV  A+  L +M +YT  +  +HM Y+FELL  D  
Sbjct: 246 PQTIQFIEALRQLINRYPGTVTLGEV-SAEDSLAVMAAYTKGDDRLHMAYSFELLTDD-Y 303

Query: 319 TASRLAEVFAEVDRVAANGWACWAFSNHDVIRHSSRWGLNPAAQ---RLFTTMMMCLRGT 375
           +A+ + +    ++    +GW CWA  NHDV R +SRWG         ++   M+  LRG+
Sbjct: 304 SAAYIRQTVEALENSIGDGWPCWAIGNHDVQRVASRWGRGKQTSDMAKMLNAMLCSLRGS 363

Query: 376 TCIYQGEELGLPEADIAFEDLQDPYGIEFWPEFKGRDGCRTPMVWEPSNGSGGFSAGKPW 435
            C YQGEELGL E  I F +LQDP+G  FWP FKGRDGCRTPM WE      GFS   PW
Sbjct: 364 VCSYQGEELGLTEVPIEFHELQDPFGKTFWPMFKGRDGCRTPMPWEQYADFSGFSQVSPW 423

Query: 436 LPVSPEHLNLSVASQEADPDAMLHHYRRAIALRKAHPALAVGTHDQLRAEGNVAFFTRQD 495
           LP++  H  L+V  QEAD  ++LH YR+ +A RK +PAL     + L A   +  F R+ 
Sbjct: 424 LPIAAAHRALAVDLQEADCHSVLHGYRQFLAWRKCYPALITSEIEFLDAPEPLLVFVRKL 483

Query: 496 RDEVIFCAFNLGDIPAEITL 515
            ++ +   FNL D   +++L
Sbjct: 484 GEQKLLVCFNLLDAETQLSL 503


Lambda     K      H
   0.321    0.137    0.444 

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: 931
Number of extensions: 45
Number of successful extensions: 4
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: 552
Length of database: 540
Length adjustment: 35
Effective length of query: 517
Effective length of database: 505
Effective search space:   261085
Effective search space used:   261085
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 (21.9 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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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources