GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Caulobacter crescentus NA1000

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate CCNA_01670 CCNA_01670 sulfate transport ATP-binding protein cysA

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Caulo:CCNA_01670
          Length = 339

 Score =  214 bits (544), Expect = 4e-60
 Identities = 128/309 (41%), Positives = 178/309 (57%), Gaps = 16/309 (5%)

Query: 19  GDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSAQ 78
           G   A+ ++ L+I DGE L L+GPSG GK+T LR +AGLE    G++  + + +   SA 
Sbjct: 13  GRYPALNKVDLEIADGELLALLGPSGSGKTTLLRTIAGLEFPDAGQVLFDGQDVTYASAA 72

Query: 79  DRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDD---EIRQRVEETTDMLGISDLLDR 135
            R +  VFQ YAL+ H +V  N++FGL+   G       EI +RVEE   ++ +  L  R
Sbjct: 73  ARRVGFVFQQYALFKHMTVAKNIAFGLDVRKGKDKPSKAEIARRVEELLKLVELEGLGGR 132

Query: 136 KPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVY 195
            P QLSGGQ+QRVAL RA+   P V L+DEP   LDA +R  +R EL+R+    GVTT++
Sbjct: 133 YPSQLSGGQRQRVALSRALAVQPSVLLLDEPFGALDATVRKSLRRELRRVHDATGVTTIF 192

Query: 196 VTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSLSGD 255
           VTHDQ EA+ + DRVA+L++G ++Q+GTP   +  P   FV GF+GE   N FDG +SG 
Sbjct: 193 VTHDQEEALELADRVAILNNGRIEQIGTPDQVHDAPETAFVCGFVGE--ANRFDGQVSGG 250

Query: 256 TFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRTFDAEVVVVEPQGNEN 315
            F+      P S A +D   GA+  T  +RP D  + E       F+  +   + QG   
Sbjct: 251 RFKAGALTVPAS-ALKD---GAA--TAYVRPHDFALDE-----AGFEVLIERAQVQGALT 299

Query: 316 AVHLRFVDG 324
           AV     DG
Sbjct: 300 AVTALTSDG 308


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: 383
Number of extensions: 21
Number of successful extensions: 3
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: 339
Length adjustment: 29
Effective length of query: 354
Effective length of database: 310
Effective search space:   109740
Effective search space used:   109740
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