GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Dyella japonica UNC79MFTsu3.2

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  275 bits (704), Expect = 1e-78
 Identities = 172/373 (46%), Positives = 229/373 (61%), Gaps = 27/373 (7%)

Query: 1   MGQIQLTDLTKRFGDT-VAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGD 59
           M +++L  L K + +  V V + S +I D E LVLVGPSGCGK+T LRM+AGLE+ + G 
Sbjct: 1   MAKVRLDKLRKVYPNGHVGVAEASFEIADGELLVLVGPSGCGKTTLLRMIAGLESISGGT 60

Query: 60  IYIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVA 119
           + IG   +N   P++RDIAMVFQ+YALYPHMTV +N+ FGL+   G   AE + RV E A
Sbjct: 61  LSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLKLR-GQPKAEIERRVAEAA 119

Query: 120 ETLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQN 179
             L +   LD +P  LSGGQ+QRVALGRA+VRDP+VFL+DEPLSNLDAKLR  MR E+  
Sbjct: 120 RMLELEQRLDSRPAALSGGQRQRVALGRALVRDPKVFLLDEPLSNLDAKLRLSMRVEIAR 179

Query: 180 LQDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPM 239
           +  +L  T VYVTH+Q EAMT+  RI V++ G +QQ+ +P   Y  P NLFVA F+G P 
Sbjct: 180 IHQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFLGSPA 239

Query: 240 INLVRGTRSESTFVGEHFSYPLDEDV---------MESVDDRDDFVLGVRPEDIEV-ADA 289
           +NL+RG        G   + P  E V         +E+  DR D V+G+RPED+ + ADA
Sbjct: 240 MNLLRGILYRDG--GWKLAMPQGELVLGELPQGAALEAWRDR-DIVVGLRPEDLLLCADA 296

Query: 290 APDDAALDDHDLQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDRVTV 349
           A   AA     L   + VVEP G++  L+L H      + AL +      L   G  +  
Sbjct: 297 A--GAA-----LAAQLEVVEPVGNEVFLNLRH-----GELALVSRMPPRELPAPGSTLHF 344

Query: 350 TIPPDKIHLFDAE 362
              P+++H FDA+
Sbjct: 345 GFAPERLHFFDAK 357


Lambda     K      H
   0.317    0.135    0.386 

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: 331
Number of extensions: 10
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: 364
Length adjustment: 30
Effective length of query: 353
Effective length of database: 334
Effective search space:   117902
Effective search space used:   117902
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: 41 (21.6 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