GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Cupriavidus basilensis 4G11

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate RR42_RS18590 RR42_RS18590 hypothetical protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Cup4G11:RR42_RS18590
          Length = 359

 Score =  300 bits (768), Expect = 4e-86
 Identities = 170/355 (47%), Positives = 226/355 (63%), Gaps = 16/355 (4%)

Query: 19  GDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSAQ 78
           G    +  + +DI DG+F VLVGPSGCGKST LRM+AGLE +T GE+ + +RV+N +  +
Sbjct: 14  GSTQVIRGVDIDIADGQFTVLVGPSGCGKSTLLRMIAGLEEITTGEIAIGNRVVNRLPPK 73

Query: 79  DRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKPG 138
           +RDIAMVFQ+YALYPH +V  NM+F L+ + G   +EI+++V + + +LG+  LL+R P 
Sbjct: 74  ERDIAMVFQNYALYPHMTVYDNMAFSLKLAKG-DKEEIKRKVAKASAILGLDSLLERYPR 132

Query: 139 QLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYVTH 198
           QLSGGQ+QRVA+GRAIVRDP+VFL DEPLSNLDAKLR +MR E++ L   L  T+VYVTH
Sbjct: 133 QLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRAEIKELHQRLRTTSVYVTH 192

Query: 199 DQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSL---SGD 255
           DQ EAMTM D++ V+ DG ++Q G PL  Y  P+NLFVAGFIG P+MN   G L    GD
Sbjct: 193 DQIEAMTMADQIVVMRDGRVEQRGKPLALYDHPDNLFVAGFIGSPAMNFVPGVLRRSGGD 252

Query: 256 TF--RGDGFDYPLSGATRDQLGGASG--LTLGIRPEDVTVGERRSGQRTFDAEVVVVEPQ 311
                 DG   P + A  D   G  G  +  G+RPE +T+G    G +T    V VVEP 
Sbjct: 253 AAVEFPDGTRLP-APARFDATAGTDGQRVIYGVRPEHLTLGMPGQGLQT---RVSVVEPT 308

Query: 312 GNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDGETGDAL 366
           G    ++ RF +     +F +    +    AGD   +       HLFD ++G  L
Sbjct: 309 GANTEIYSRFCE----AEFISIFRERHDFAAGDILNLVPDHQHTHLFDADSGQTL 359


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: 448
Number of extensions: 26
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: 359
Length adjustment: 30
Effective length of query: 353
Effective length of database: 329
Effective search space:   116137
Effective search space used:   116137
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