GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Desulfobacter vibrioformis DSM 8776

Align ABC transporter substrate-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized)
to candidate WP_035236789.1 Q366_RS04660 ABC transporter substrate-binding protein

Query= TCDB::Q8DQI1
         (386 letters)



>NCBI__GCF_000745975.1:WP_035236789.1
          Length = 381

 Score =  143 bits (361), Expect = 7e-39
 Identities = 110/353 (31%), Positives = 171/353 (48%), Gaps = 11/353 (3%)

Query: 35  SVEEKTIKIGFNFEESGSLAAYGTAEQKGAQLAVDEINAAGGIDGKQIEVVDKDNKSETA 94
           +V     KIG  F  +G  +  G  E+K  ++ V++INAAGGIDG ++E V  D++ + A
Sbjct: 23  AVAADVYKIGGIFSVTGRASFLGDPEKKTMEMMVEQINAAGGIDGHRLEAVIYDSEGDPA 82

Query: 95  EAASVTTNLVTQSKVSAVVGPATSGATAAAVANATKAGVPLISPSATQDGLTKGQDYLFI 154
           +A S    L+ + KV A++GP+T+  T A V    +  VPLIS +A     T    ++F 
Sbjct: 83  KAVSAVNKLLHKDKVIAIIGPSTTPTTLAIVNFTKREKVPLISCAAGIKITTPVDPWVFK 142

Query: 155 GTFQDSFQGKIISNYVSEKLNAKKVVLYTDNA-SDYAKGIAKSFRESYKGEIVADETFVA 213
               D      +   +      K  +L   NA  +  K    S  E +  ++V +E+F A
Sbjct: 143 TAQSDLLAVAAVYQQMKTAGIKKIGILTVSNAYGESGKKQLLSQAEKFGIQVVLNESFGA 202

Query: 214 GDTDFQAALTKMKGKDFDAIVVPGYYNEAGKIVNQARGMGIDKPIVGGDGFNGEEFVQQA 273
            DTD  A L K+K    DAIV  G       +   A+ + ID P+    G    +F++ A
Sbjct: 203 KDTDTTAQLAKIKAAGPDAIVCWGTNPGPAVVAKNAKQLKIDIPLYQSHGVGSPKFIELA 262

Query: 274 TAEKASNI-----YFISGFSTTVEVSAKA-KAFLDAYRAKYNEEPSTFAALAYDSVHLVA 327
                 NI       ++      +   K  + +  AY+ K++   S F   AYD+V+L+A
Sbjct: 263 GDAANGNILPTGKILVTSLLDDTDPQKKVLEDYQKAYQNKFSGNVSGFGGYAYDAVNLLA 322

Query: 328 NAAKGAKNSGE-IKNNLAKTKDFEGVTGQTSFDA-DHNTVKTA--YMMTMNNG 376
           NA KG+    E I++NL  TK + G TG+ +F A DHN +  A   M+ + NG
Sbjct: 323 NALKGSSGDKEKIRDNLEATKGYVGATGEFNFTAQDHNGLSPAAFVMVEIQNG 375


Lambda     K      H
   0.310    0.126    0.337 

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: 314
Number of extensions: 11
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: 386
Length of database: 381
Length adjustment: 30
Effective length of query: 356
Effective length of database: 351
Effective search space:   124956
Effective search space used:   124956
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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