GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00885 in Halomonas desiderata SP1

Align ABC-type branched-chain amino acid transport system, permease component protein (characterized, see rationale)
to candidate WP_086509603.1 BZY95_RS08775 urea ABC transporter permease subunit UrtB

Query= uniprot:D8IUY4
         (309 letters)



>NCBI__GCF_002151265.1:WP_086509603.1
          Length = 524

 Score =  137 bits (345), Expect = 6e-37
 Identities = 90/298 (30%), Positives = 162/298 (54%), Gaps = 21/298 (7%)

Query: 11  GLVLGSMYALIALGYTMVYGVLNLINFAHGDILMVGAMVGLSLLKVVQQVAPGLPGIVQL 70
           GL LGS+  L A+G  + +GV+ +IN AHG+++M+GA    ++    QQ+ PG PG+  L
Sbjct: 238 GLSLGSVLVLAAIGLAITFGVMGVINMAHGELIMLGAYTTWAM----QQLLPGQPGLA-L 292

Query: 71  VIAIVGAIPVCIVVSLLIERIAYRPLRNAPRLAPLITAIGVSILLQTLAMMIWGRSPLPF 130
           ++AI     V  +  + IER   + L+  P L  L+   G+S++LQ L     G SPL  
Sbjct: 293 ILAIPAGFLVAALAGIAIERGVIQFLKGRP-LETLLATFGISLILQQLVRT--GISPLNR 349

Query: 131 PQVMP---SDPVHIAGAL-ISPTQIMLLALAVLAMVGLVLIVEKTKMGRAMRATAENPRI 186
             + P   S  + +  AL ++  ++ +L  A++    L+LI+ +T++G  +RA  +N  +
Sbjct: 350 TVITPEWMSGSIAVNDALSLTLNRMYVLGFALVVFAVLMLIMRRTRLGLEVRAVTQNRAM 409

Query: 187 AGLMGVDANKVIVVTFAIGAGLAAIAGVMWAANYSTAQFAMGFVPGLKAFSAAVLGGIGN 246
           A  MG+ A +V ++TFA+G+G+A +AGV   +  +     +G    + +F   V GG+GN
Sbjct: 410 ARSMGIRATRVDIMTFALGSGVAGLAGVA-LSQLTNVGPNLGQNYIIDSFMVVVFGGVGN 468

Query: 247 IYGAMLGGILLGLIESLGAGYIGDLTGNFLGSNYQDIFAFIVLIIVLTLRPSGIMGER 304
           ++G ++ G+ LG+I  +   + G +           I   + +I+ +  RP G+  ++
Sbjct: 469 LWGTLVAGLSLGVINQVLEPWAGAVMAK--------IIVLVFIILFIQKRPRGLFPQK 518


Lambda     K      H
   0.328    0.144    0.416 

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: 354
Number of extensions: 14
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: 309
Length of database: 524
Length adjustment: 31
Effective length of query: 278
Effective length of database: 493
Effective search space:   137054
Effective search space used:   137054
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 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