GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Nocardioides dokdonensis FR1436

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_068109002.1 I601_RS10130 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:D4GP39
         (383 letters)



>NCBI__GCF_001653335.1:WP_068109002.1
          Length = 400

 Score =  330 bits (847), Expect = 3e-95
 Identities = 183/386 (47%), Positives = 243/386 (62%), Gaps = 25/386 (6%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA +TL ++ K Y    G    AV ++S+DI DGEF++LVGPSGCGKST LRM+ GLE +
Sbjct: 1   MAAITLKNIVKKY----GDGFPAVNDVSIDIADGEFVILVGPSGCGKSTLLRMIVGLEDI 56

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
           T G++ + DR +N ++ +DR++AMVFQ+YALYPH SV  N++F L  + G P+ EI ++V
Sbjct: 57  TSGDMMIGDRKVNDLAPRDRNLAMVFQNYALYPHLSVYENIAFPLRLA-GAPEKEIDEKV 115

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
            E +  L + + L+RKPG LSGGQ+QRVA+GRAIVR  + FL DEPLSNLDAKLR +MRT
Sbjct: 116 REASKTLELDEHLERKPGNLSGGQRQRVAMGRAIVRQADAFLFDEPLSNLDAKLRGQMRT 175

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E+ RLQ  LG+TTVYVTHDQTEAMT+GDRVAVL  G LQQ+ TP + Y  P NLFVAGFI
Sbjct: 176 EIARLQKRLGITTVYVTHDQTEAMTLGDRVAVLKRGLLQQLATPRELYENPGNLFVAGFI 235

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRP---EDVTVGERRSG 297
           G P MN     + G + +       +  A  ++  G   L  GIRP   ED T+ ++   
Sbjct: 236 GSPPMNFLPAEVEGTSVKLPFGTVQIPEAKAERCQGKGVLMAGIRPEYFEDATIADKVGS 295

Query: 298 QRTFDAEVVVVEPQGNENAVHLRF----------------VDGDE-GTQFTATTTGQSRV 340
             TF A+V  VE  GNE   ++ F                +DG+   TQ   +  G SR+
Sbjct: 296 DSTFSADVDYVEWLGNETYAYIPFEAPPEVEAKMRELEADLDGEGLRTQLVVSLDGASRI 355

Query: 341 EAGDRTTVSFPEDAIHLFDGETGDAL 366
           + G+   +      +HLFD  TG+ L
Sbjct: 356 KEGETAEIWVDATKMHLFDPATGENL 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: 488
Number of extensions: 22
Number of successful extensions: 4
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: 400
Length adjustment: 31
Effective length of query: 352
Effective length of database: 369
Effective search space:   129888
Effective search space used:   129888
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 24 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