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_RS16715 HSERO_RS16715 sugar ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__HerbieS:HSERO_RS16715
          Length = 361

 Score =  310 bits (793), Expect = 5e-89
 Identities = 175/358 (48%), Positives = 224/358 (62%), Gaps = 17/358 (4%)

Query: 19  GDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSAQ 78
           G    +  + +DI DGEF VLVGPSGCGKST LRM+AGLE +T GE+ +   V+N V  +
Sbjct: 14  GSTQIIRGVDIDIADGEFTVLVGPSGCGKSTLLRMLAGLEEITGGEILIGGTVVNNVQPK 73

Query: 79  DRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDE--IRQRVEETTDMLGISDLLDRK 136
           DRDIAMVFQ+YALYPH +VR NM+F L   T    D+  + +RV++  D+LG++ LLDR 
Sbjct: 74  DRDIAMVFQNYALYPHMTVRDNMAFSL---TLAKKDKAFVDERVKKAADILGLNQLLDRY 130

Query: 137 PGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYV 196
           P QLSGGQ+QRVA+GRAIVRDP+VFL DEPLSNLDAKLR +MRTE++ L   L  T++YV
Sbjct: 131 PRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRTEIKELHQRLKTTSIYV 190

Query: 197 THDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSL---- 252
           THDQ EAMTM D++ V+ DG ++Q G PLD Y  P NLFVAGFIG P+MN    +L    
Sbjct: 191 THDQIEAMTMADQIVVMRDGLVEQRGRPLDLYDYPANLFVAGFIGSPAMNFIPATLRRNA 250

Query: 253 -SGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRTFDAEVVVVEPQ 311
              +    DG   P       Q      +T G+RPE +++G    G  T   +V+VVEP 
Sbjct: 251 TGAEVEFADGTRVPAPYGAALQGNDGQKVTYGVRPEHLSIGAAGQGIAT---KVIVVEPT 307

Query: 312 GNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDGETGDALKNR 369
           G +  V  RF D    T  T+    +    AGD   +       HLFD E+G +L  R
Sbjct: 308 GADTEVFSRFGD----TSLTSIFRERHDFGAGDVIHLVPDHSRTHLFDAESGKSLAGR 361


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: 438
Number of extensions: 23
Number of successful extensions: 5
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: 361
Length adjustment: 30
Effective length of query: 353
Effective length of database: 331
Effective search space:   116843
Effective search space used:   116843
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: 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