GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Herbaspirillum seropedicae SmR1

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate HSERO_RS01355 HSERO_RS01355 sugar ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__HerbieS:HSERO_RS01355
          Length = 381

 Score =  286 bits (733), Expect = 5e-82
 Identities = 174/394 (44%), Positives = 230/394 (58%), Gaps = 28/394 (7%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA +TL    K Y D        +  + LDI + EF V +GPSGCGKST LR +AGLE +
Sbjct: 1   MASITLRAAQKAYGDAPP----VIRNVDLDIGEHEFCVFLGPSGCGKSTLLRSIAGLEDL 56

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           T G+L +  + +N V +  R +AMVFQSYAL+PH +V  NMSFGL  +  LP  EI Q+V
Sbjct: 57  TSGDLFIGGKRVNDVPSAQRSVAMVFQSYALFPHMTVYENMSFGLTLAK-LPKAEIEQKV 115

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            E   +L + +LL RKP +LSGGQ+QRVA+GRAIVR P VFL DEPLSNLDA LR++ R 
Sbjct: 116 REAARILQLEELLQRKPKELSGGQRQRVAIGRAIVRRPGVFLFDEPLSNLDATLRSQTRI 175

Query: 181 ELQRLQGEL-GVTTVYVTHDQTEAMTMGDRVAVLDD-------GELQQVGTPLDCYHRPN 232
           E+ RL  +    + VYVTHDQ EAMT+ DR+ +L         G + QVGTP++ YH P 
Sbjct: 176 EIARLHRQFEQASVVYVTHDQVEAMTLADRIVLLHAGADTQRFGSIAQVGTPMELYHHPR 235

Query: 233 NLFVAGFIGEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASG-------LTLGIR 285
           N FVAGFIG P MN     ++G   + +G    LSG+    L  A G       +T+G+R
Sbjct: 236 NRFVAGFIGSPRMNFLPAQVAG--VQENGILVRLSGSEETLLVAAQGALQPGQMVTVGVR 293

Query: 286 PEDVTVGERRSGQRTFDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDR 345
           PE + +G +  GQ     EVV+VE  G +  VHL   D   G    A   G +R+  G+R
Sbjct: 294 PEHMEIGSQ--GQYGIHREVVLVERLGEQTYVHL---DEPAGQPLVAKAAGDARITRGER 348

Query: 346 TTVSFPEDAIHLFDGETGDALKNRELPSNRAIDA 379
             V+      +LFD + G AL   ++    A+ A
Sbjct: 349 VRVAIAPACAYLFD-QDGLALTRTQVQGGLAVAA 381


Lambda     K      H
   0.316    0.136    0.384 

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: 408
Number of extensions: 21
Number of successful extensions: 7
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: 383
Length of database: 381
Length adjustment: 30
Effective length of query: 353
Effective length of database: 351
Effective search space:   123903
Effective search space used:   123903
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: 42 (22.0 bits)
S2: 50 (23.9 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