Aligments for a candidate for rbsA in Acidovorax sp. GW101-3H11

GapMind for catabolism of small carbon sources

Aligments for a candidate for rbsA in Acidovorax sp. GW101-3H11

Align ribose transport, ATP-binding protein RbsA; EC 3.6.3.17 (characterized)
to candidate Ac3H11_2431 ABC transporter ATP-binding protein

Query= CharProtDB::CH_003578
         (501 letters)



>lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_2431 ABC transporter
           ATP-binding protein
          Length = 514

 Score =  257 bits (657), Expect = 6e-73
 Identities = 175/520 (33%), Positives = 270/520 (51%), Gaps = 36/520 (6%)

Query: 1   MEALLQLKGIDKAFPGVKALSGAALNVYPGRVMALVGENGAGKSTMMKVLTGIYTRDAGT 60
           M  +L+L  I K F  + A    +L +  G V+AL+GENGAGKST+M +L G Y  D G+
Sbjct: 1   MSNVLRLSHITKRFGKLVANDSISLTLARGEVLALLGENGAGKSTLMSILFGHYVADEGS 60

Query: 61  LLWLGKETTFTGPKSSQEAGIGIIHQELNLIPQLTIAENIFLGREFVNRFGKIDWKTMYA 120
           +   G+      P+++  AGIG++HQ   L   LT+ +N+ LG E +       W+    
Sbjct: 61  IEVFGQPLPPGQPRAALAAGIGMVHQHFTLADNLTVLDNVLLGSEPL-------WQPFSR 113

Query: 121 EAD---KLLA---KLNLRFKSDKLVGDLSIGDQQMVEIAKVLSFESKVIIMDEPTDALTD 174
            ++   KLLA   +  L    D  VG LS+G++Q VEI K L   + ++I+DEPT  LT 
Sbjct: 114 RSEARAKLLAVSQQFGLPVSPDAKVGSLSVGERQRVEILKALYRGAHILILDEPTAVLTP 173

Query: 175 TETESLFRVIRELKSQGRGIVYISHRMKEIFEICDDVTVFRDGQFIAEREVASLTEDSLI 234
            E+E+LF  + ++ +QG  I++ISH++ E+  +   V V R G+ +AE      T+  L 
Sbjct: 174 QESEALFDTLAQMVAQGLSIIFISHKLGEVLRVSHRVAVLRQGKLVAEAPAQGTTQGQLA 233

Query: 235 EMMVGRKLEDQYPHLDKAPGDIRLKVDNL-CGPG----VNDVSFTLRKGEILGVSGLMGA 289
           + MVG  +E       +  G+    + N+   P     +NDVS TLR GEI+ ++G+ G 
Sbjct: 234 QWMVGHAIEAAERRPAQNVGEPICTLSNVSTAPAGRDRLNDVSLTLRAGEIVAIAGVSGN 293

Query: 290 GRTELMKVLYGALPRTSGYVTLDGHEVVTRSPQDGLANGIVYISEDRKRDGLVLGMSVKE 349
           G+  L  VL G    T+G VTL G  +  R P   ++ G+  I EDR   G+V  + V E
Sbjct: 294 GQVALADVLCGVRAATTGQVTLRGAPLQAR-PAWLVSQGVARIPEDRHAVGVVGDLPVWE 352

Query: 350 NMSLTALR--YFS----RAGGSLKHADEQQAVSDFIRLFNVKTPSMEQAIGLLSGGNQQK 403
           N     LR  +F+    RA    + A  Q A       F+V+    +     LSGGN QK
Sbjct: 353 NAVSERLRGPWFAHPWFRAFWVKRRAARQHA-QRVAETFDVRGGGADAPARSLSGGNMQK 411

Query: 404 VAIARGLMTR----------PKVLILDEPTRGVDVGAKKEIYQLINQFKADGLSIILVSS 453
           + + R LM            P++++  +PT G+D+GA   + Q +   +  G +++L+S 
Sbjct: 412 LILGRALMPPQDAAGNSAPVPQLIVAHQPTWGLDIGAVMFVQQQLINARDSGAAVLLISD 471

Query: 454 EMPEVLGMSDRIIVMHEGHLSGEFTREQATQEVLMAAAVG 493
           ++ EVL + DR+ VMH+G LS     E  T+E +  A  G
Sbjct: 472 DLDEVLALGDRVAVMHDGRLSEALPAEGWTREAIGLAMAG 511


Lambda     K      H
   0.318    0.137    0.380 

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: 555
Number of extensions: 23
Number of successful extensions: 9
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: 501
Length of database: 514
Length adjustment: 34
Effective length of query: 467
Effective length of database: 480
Effective search space:   224160
Effective search space used:   224160
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 (21.7 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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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 paper from 2022 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