GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Paucidesulfovibrio gracilis DSM 16080

Align Leucine-, isoleucine-, valine-, threonine-, and alanine-binding protein; LIVAT-BP; Leu/Ile/Val/Thr/Ala-binding protein (characterized)
to candidate WP_200806748.1 B5D49_RS00095 branched-chain amino acid ABC transporter substrate-binding protein

Query= SwissProt::P21175
         (373 letters)



>NCBI__GCF_900167125.1:WP_200806748.1
          Length = 395

 Score =  230 bits (587), Expect = 4e-65
 Identities = 127/338 (37%), Positives = 191/338 (56%), Gaps = 3/338 (0%)

Query: 27  ADTIKIALAGPVTGPVAQYGDMQRAGALMAIEQINKAGGVNGAQLEGVIYDDACDPKQAV 86
           A  I + + G  +G +A YG      A +  E+IN  GGV G  ++ V  DD C P++A 
Sbjct: 49  AGEIVLGVPGAHSGDLASYGLPTVNAAELVAEKINAEGGVLGRMVKVVAQDDECKPEKAT 108

Query: 87  AVANKVVNDGVKFVVGHVCSSSTQPATDIYEDEGVLMITPSATAPEITSRG-YKLIFRTI 145
             A K++++GV  V+GH+CS +T+ A  IY +  ++ ++PSAT P +T  G Y   FRTI
Sbjct: 109 NAATKLLSEGVHVVLGHICSGATKAALPIYTETRIVCMSPSATNPPLTQSGDYPNFFRTI 168

Query: 146 GLDNMQGPVAGKFIAERYKDKTIAVLHDKQQYGEGIATEVKKTVE-DAGIKVAVFEGLNA 204
             D+ Q  +   F A++    TIAV+HDK  YG+G A+  +  VE D  + V +FEG+  
Sbjct: 169 ASDDAQAQLGVDF-AKKIGLTTIAVIHDKGDYGKGFASFARDFVEADPDMNVVLFEGVTP 227

Query: 205 GDKDFNALISKLKKAGVQFVYFGGYHPEMGLLLRQAKQAGLDARFMGPEGVGNSEITAIA 264
           G  D++A++ K+K +G   V FGGYHPE   ++ Q ++  LD  F+  +GV +     +A
Sbjct: 228 GAVDYSAVVQKIKNSGADGVIFGGYHPEASKIVSQMRKKDLDLPFISDDGVKDDTFIKVA 287

Query: 265 GDASEGMLATLPRAFEQDPKNKALIDAFKAKNQDPSGIFVLPAYSAVTVIAKGIEKAGEA 324
           G+ +EG+ A+ PR    +P  +  +DA KAK     G F   AYSA   +   IEKAG  
Sbjct: 288 GEYAEGVYASGPRDISGNPLYQVALDAHKAKYGTEPGAFFYEAYSAALALLNAIEKAGST 347

Query: 325 DPEKVAEALRANTFETPTGNLGFDEKGDLKNFDFTVYE 362
           D + V  ALR    +TP G + FD KGD +   F++Y+
Sbjct: 348 DYDAVVNALRTEYVDTPVGKIKFDAKGDAEGVGFSMYQ 385


Lambda     K      H
   0.316    0.133    0.377 

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: 378
Number of extensions: 24
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: 373
Length of database: 395
Length adjustment: 30
Effective length of query: 343
Effective length of database: 365
Effective search space:   125195
Effective search space used:   125195
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 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