Alignments for a candidate for araVsh in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Alignments for a candidate for araVsh in Escherichia coli BW25113

Align ABC transporter related (characterized, see rationale)
to candidate 17809 b3749 fused D-ribose transporter subunits of ABC superfamily: ATP-binding components (NCBI)

Query= uniprot:A0KWY5
         (499 letters)



>FitnessBrowser__Keio:17809
          Length = 501

 Score =  349 bits (895), Expect = e-100
 Identities = 193/503 (38%), Positives = 314/503 (62%), Gaps = 14/503 (2%)

Query: 1   MSLILELKQISKHYPGVKALEDVSLRLFAGEVHALLGENGAGKSTLVKVMTGAQSKDMGD 60
           M  +L+LK I K +PGVKAL   +L ++ G V AL+GENGAGKST++KV+TG  ++D G 
Sbjct: 1   MEALLQLKGIDKAFPGVKALSGAALNVYPGRVMALVGENGAGKSTMMKVLTGIYTRDAGT 60

Query: 61  ILFLGEPQHFNTPMDAQKAGISTVYQEVNLVPNLTVAQNLFLGYE-PRRLGLIHFKKMYA 119
           +L+LG+   F  P  +Q+AGI  ++QE+NL+P LT+A+N+FLG E   R G I +K MYA
Sbjct: 61  LLWLGKETTFTGPKSSQEAGIGIIHQELNLIPQLTIAENIFLGREFVNRFGKIDWKTMYA 120

Query: 120 DARAVLTQFKLDIDVSAPLSDYSIAVQQLIAIARGVAMSAKVLVLDEPTASLDAKEVQVL 179
           +A  +L +  L       + D SI  QQ++ IA+ ++  +KV+++DEPT +L   E + L
Sbjct: 121 EADKLLAKLNLRFKSDKLVGDLSIGDQQMVEIAKVLSFESKVIIMDEPTDALTDTETESL 180

Query: 180 FGILNQLKAKGVAIVFITHFLDQVYQISDRITVLRNGQFIGEYLTAELPQPKLIEAMLGR 239
           F ++ +LK++G  IV+I+H + ++++I D +TV R+GQFI E   A L +  LIE M+GR
Sbjct: 181 FRVIRELKSQGRGIVYISHRMKEIFEICDDVTVFRDGQFIAEREVASLTEDSLIEMMVGR 240

Query: 240 SLQEQL--VDKQEKERTVTRAEAVLLSLEDVSVKGSIQSMNLTVPKGQAVGLAGLLGSGR 297
            L++Q   +DK   +        + L ++++   G +  ++ T+ KG+ +G++GL+G+GR
Sbjct: 241 KLEDQYPHLDKAPGD--------IRLKVDNLCGPG-VNDVSFTLRKGEILGVSGLMGAGR 291

Query: 298 SEVCNAVFGLDLVDSGSIHLAGQKLNLSQPVDAISAGIALCPEDRKIDGIIGPLSIRENI 357
           +E+   ++G     SG + L G ++    P D ++ GI    EDRK DG++  +S++EN+
Sbjct: 292 TELMKVLYGALPRTSGYVTLDGHEVVTRSPQDGLANGIVYISEDRKRDGLVLGMSVKENM 351

Query: 358 IL-ALQARIGWWRYLSNTRQQEIAQFFIDKLQIATPDADKPIEQLSGGNQQKVILARWLA 416
            L AL+        L +  +Q+    FI    + TP  ++ I  LSGGNQQKV +AR L 
Sbjct: 352 SLTALRYFSRAGGSLKHADEQQAVSDFIRLFNVKTPSMEQAIGLLSGGNQQKVAIARGLM 411

Query: 417 IEPILLVLDEPTRGIDIGAHAEIVKLIRTLCDEGMSLLVASSELDELVAFSNKVVVLRDR 476
             P +L+LDEPTRG+D+GA  EI +LI     +G+S+++ SSE+ E++  S++++V+ + 
Sbjct: 412 TRPKVLILDEPTRGVDVGAKKEIYQLINQFKADGLSIILVSSEMPEVLGMSDRIIVMHEG 471

Query: 477 YAVRELSGAELTSQHVMQAIAEG 499
           +   E +  E  +Q V+ A A G
Sbjct: 472 HLSGEFT-REQATQEVLMAAAVG 493



 Score =  102 bits (255), Expect = 2e-26
 Identities = 73/236 (30%), Positives = 121/236 (51%), Gaps = 18/236 (7%)

Query: 15  PGVKALEDVSLRLFAGEVHALLGENGAGKSTLVKVMTGAQSKDMGDILFLGEPQHFNTPM 74
           PGV    DVS  L  GE+  + G  GAG++ L+KV+ GA  +  G +   G      +P 
Sbjct: 266 PGVN---DVSFTLRKGEILGVSGLMGAGRTELMKVLYGALPRTSGYVTLDGHEVVTRSPQ 322

Query: 75  DAQKAGISTVYQEVN---LVPNLTVAQNLFLG---YEPRRLGLIHFKKMYADARAVLTQF 128
           D    GI  + ++     LV  ++V +N+ L    Y  R  G +     +AD +  ++ F
Sbjct: 323 DGLANGIVYISEDRKRDGLVLGMSVKENMSLTALRYFSRAGGSLK----HADEQQAVSDF 378

Query: 129 KLDIDVSAPLSDYSIAV-----QQLIAIARGVAMSAKVLVLDEPTASLDAKEVQVLFGIL 183
               +V  P  + +I +     QQ +AIARG+    KVL+LDEPT  +D    + ++ ++
Sbjct: 379 IRLFNVKTPSMEQAIGLLSGGNQQKVAIARGLMTRPKVLILDEPTRGVDVGAKKEIYQLI 438

Query: 184 NQLKAKGVAIVFITHFLDQVYQISDRITVLRNGQFIGEYLTAELPQPKLIEAMLGR 239
           NQ KA G++I+ ++  + +V  +SDRI V+  G   GE+   +  Q  L+ A +G+
Sbjct: 439 NQFKADGLSIILVSSEMPEVLGMSDRIIVMHEGHLSGEFTREQATQEVLMAAAVGK 494


Lambda     K      H
   0.319    0.136    0.377 

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: 582
Number of extensions: 32
Number of successful extensions: 8
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: 499
Length of database: 501
Length adjustment: 34
Effective length of query: 465
Effective length of database: 467
Effective search space:   217155
Effective search space used:   217155
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 (21.8 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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 paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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